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US20200276088A1 - Devices, system and method to control the delivery of oral medications to ensure they are efficacious, taken as prescribed, and to avoid unwanted side effects - Google Patents

Devices, system and method to control the delivery of oral medications to ensure they are efficacious, taken as prescribed, and to avoid unwanted side effects Download PDF

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US20200276088A1
US20200276088A1 US16/858,451 US202016858451A US2020276088A1 US 20200276088 A1 US20200276088 A1 US 20200276088A1 US 202016858451 A US202016858451 A US 202016858451A US 2020276088 A1 US2020276088 A1 US 2020276088A1
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drug
patient
app
information
specific
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US16/858,451
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Edmund L. Valentine
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Accoy Pharmaceuticals Inc
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Accoy Pharmaceuticals Inc
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    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
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    • G16H70/00ICT specially adapted for the handling or processing of medical references
    • G16H70/40ICT specially adapted for the handling or processing of medical references relating to drugs, e.g. their side effects or intended usage
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    • A61J7/00Devices for administering medicines orally, e.g. spoons; Pill counting devices; Arrangements for time indication or reminder for taking medicine
    • A61J7/04Arrangements for time indication or reminder for taking medicine, e.g. programmed dispensers
    • A61J7/0409Arrangements for time indication or reminder for taking medicine, e.g. programmed dispensers with timers
    • A61J7/0418Arrangements for time indication or reminder for taking medicine, e.g. programmed dispensers with timers with electronic history memory
    • AHUMAN NECESSITIES
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    • A61J7/00Devices for administering medicines orally, e.g. spoons; Pill counting devices; Arrangements for time indication or reminder for taking medicine
    • A61J7/04Arrangements for time indication or reminder for taking medicine, e.g. programmed dispensers
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    • A61J7/0427Arrangements for time indication or reminder for taking medicine, e.g. programmed dispensers with timers with direct interaction with a dispensing or delivery system
    • A61J7/0445Arrangements for time indication or reminder for taking medicine, e.g. programmed dispensers with timers with direct interaction with a dispensing or delivery system for preventing drug dispensing during a predetermined time period
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    • A61J7/00Devices for administering medicines orally, e.g. spoons; Pill counting devices; Arrangements for time indication or reminder for taking medicine
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    • G16H50/00ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics
    • G16H50/70ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for mining of medical data, e.g. analysing previous cases of other patients
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    • A61J2200/00General characteristics or adaptations
    • A61J2200/30Compliance analysis for taking medication
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    • A61J2200/00General characteristics or adaptations
    • A61J2200/70Device provided with specific sensor or indicating means
    • A61J2200/72Device provided with specific sensor or indicating means for temperature
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    • A61JCONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J2205/00General identification or selection means
    • A61J2205/30Printed labels
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61JCONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J2205/00General identification or selection means
    • A61J2205/60General identification or selection means using magnetic or electronic identifications, e.g. chips, RFID, electronic tags
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16HHEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H10/00ICT specially adapted for the handling or processing of patient-related medical or healthcare data
    • G16H10/20ICT specially adapted for the handling or processing of patient-related medical or healthcare data for electronic clinical trials or questionnaires
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16HHEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H15/00ICT specially adapted for medical reports, e.g. generation or transmission thereof
    • GPHYSICS
    • G16INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16HHEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H50/00ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics
    • G16H50/20ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A90/00Technologies having an indirect contribution to adaptation to climate change
    • Y02A90/10Information and communication technologies [ICT] supporting adaptation to climate change, e.g. for weather forecasting or climate simulation
    • Y02A90/26

Definitions

  • the present disclosure relates to a novel system to improve medication safety and effectiveness via the utilization of drug specific algorithms to control drug dispensing, avoid drug mediated adverse events, ensure prescription compliance and promote prescription persistence on a cost-effective real-time basis.
  • Drug-related hospitalizations account for 2.4 to 6.5 percent of all medical admissions in the general population.
  • a meta-analysis found a fourfold increase in the rate of hospitalization related to adverse drug events (ADE) in older adults compared with younger adults (16.6 versus 4.1 percent).
  • ADE adverse drug events
  • a number of factors in older individuals contribute to their increased risk for developing a drug-related problem. These include frailty, coexisting medical problems, memory issues, polypharmacy, and the use of non-prescribed medications.
  • Estimates indicate that 88 percent of the ADE hospitalizations among older adults were preventable, compared with 24 percent among young persons
  • Optimizing drug therapy is an essential part of medical care.
  • the process of prescribing a medication is complex and includes (i) deciding that a drug is indicated, (ii) choosing the best drug, (iii) determining a dose and schedule appropriate for the patient's physiologic status, (iv) monitoring for effectiveness and toxicity, (v) educating the patient about expected side effects, and (vi) indications for seeking consultation.
  • Avoidable adverse drug events are the serious consequence of (i) inappropriate drug prescribing, (ii) changes in the patient's reaction to the drug over time due to lifestyle, other medications, other medical conditions, worsening medical condition, or changes in the patients overall well-being, etc., or (iii) addition of new prescription or OTC medications, vitamins, dietary supplements, herbal medicines (e.g., ginseng, ginkgo biloba extract, glucosamine, St. John's wort, echinacea, garlic, saw palmetto, kava, and valerian root), and/or recreational drugs, etc. Often, clinicians do not question patients about use of herbal medicines and patients do not routinely volunteer this information.
  • herbal medicines e.g., ginseng, ginkgo biloba extract, glucosamine, St. John's wort, echinacea, garlic, saw palmetto, kava, and valerian root
  • recreational drugs etc.
  • clinicians do not question patients about use of
  • the same dose could lead to higher plasma concentrations in an older, compared to younger, patient.
  • the volume of distribution for diazepam is increased, and the clearance rate for lithium is reduced, in older adults.
  • increasing age may result in an increased sensitivity to the effects of certain drugs, e.g., benzodiazepines and opioids.
  • the risk of an adverse event due to drug-drug interactions is substantially increased when multiple drugs are taken.
  • the risk of bleeding with warfarin therapy is increased with coadministration of selective and non-selective NSAIDs, SSRIs, omeprazole, lipid-lowering agents, amiodarone, and fluorouracil.
  • NSAIDs selective and non-selective NSAIDs
  • SSRIs selective and non-selective NSAIDs
  • omeprazole lipid-lowering agents
  • amiodarone amiodarone
  • fluorouracil fluorouracil
  • Periodic evaluation of a patient's drug regimen is an essential component of medical care.
  • a survey of Medicare beneficiaries found that more than 30 percent of patients reported they had not talked with their doctor about their different medications in the previous 12 months.
  • these reviews are done, they often overlook OTC, supplements, herbal medicines and recreational drugs that are being taken by the patient.
  • the present invention describes novel methods and drug dispensing devices, drug specific Apps, drug specific dispensing algorithms, and an integrated support center to ensure any oral medication taken by a patient is efficacious; is only dispensed as prescribed by the healthcare professional (e.g., physician, physician's assistant, nurse practitioner, pharmacist, etc.); is not dispensed if (i) the patient is trying to take the medication sooner than the prescribed interval, (ii) the algorithm deduces that taking the drug may result in an adverse event, even if it could be dispensed within the prescription's guidelines (iii) the drug is past its expiration date, (iv) the drug was not stored properly, e.g., within the right temperature and/or humidity guidelines, and/or (v) the drug batch has been recalled, etc.; and encourages the patient to continue taking the medication as prescribed.
  • the dispensing system saves the healthcare system money by decreasing the number of interventions, physician's office visits, and hospital
  • the drug specific dispensing algorithm uses encrypted communications to control the drug dispensing device and to communicate with the patient and the support center.
  • the algorithm uses the prescription information, dispensing device information, drug cassette information, patient self-assessment and/or digitally captured physiological, psychological, lifestyle, medications currently being taken, and/or environmental data in a novel drug specific diagnostic algorithm to decide if the drug dispenser should dispense the drug or keep the tamper resistant dispensing unit locked.
  • the novel drug specific App which can be operated from a standalone drug dispensing device, interface device (smart phone, tablet and/or computer, or standalone drug dispensing device, etc. with Internet communication capabilities), reads and aggregates; (i) the drug information from the drug cassette, (ii) the devices serial number, operating, environmental and dispensing information from the dispensing device, (iii) patient self-assessment data from input screens on the standalone dispenser, smart phone, tablet, and/or computer, etc., and (iv) digital data generated by wearable devices, consumed, implanted, or injected diagnostic devices, monitoring devices, machines, instruments, gadgets, contraptions, apparatuses, utensils, implements, tools, mechanisms, and informalgizmos, etc.
  • the drug dispensing device is designed to automatically recognize the drug based upon the drug specific disposable drug cassette docked into the device.
  • the cassette is marked to allow the drug dispenser to ascertain the name of the drug (brand and/or generic), the drug's NDC number, the drug batch number, and drug's expiration date, etc.
  • the drug dispensing device is designed to be water proof, tamper resistant, withstand being dropped and/or banged, operate and withstand hot and cold temperatures within defined temperature ranges, to be reusable and rechargeable, to have the drug cassette only docked or removed by a healthcare professional, to remain locked from dispensing unless the dispensing device receives an encrypted signal from the authorized smart App, and to dispense the drug with one click.
  • the device when interfaced with the drug specific App, transmits its serial number via a secure handshake with the App, reads and transmits the drug information on the drug cassette, transmits the current and historic temperatures since the last dispense, and the date and time the drug is dispensed.
  • the drug dispensing device can be configured to dispense one or more drugs and to be controlled by one or more dispensing Apps, one App for each drug.
  • the multi-drug dispensing units utilize multiple drug cassettes (one each per drug) which are controlled by a consolidation App that combines the individual drug Apps into a single user interface to eliminate duplication of inputs and to facilitate one click drug dispensing for one or more medications.
  • the handshake between Apps is controlled by the biometric security system.
  • the single drug App as well as the multi-drug App, require biometric sign on by the patient and utilize a drug specific decision tree algorithm to make dispensing decisions.
  • An encrypted sign on alternative may also be provided. No messages or further communication with the patient are required if drug dispensing is within prescribing guidelines and no potential adverse events are detected by the algorithm. However, if the algorithm decides to keep the dispensing unit locked and not to dispense, even if within prescribing guidelines, then a number of alternative messages are shown on the interface device (standalone dispensing unit, smart phone, tablet, and/or computer, etc. with Internet communications capabilities).
  • the App uses the biometric sign on and encrypted communications with the support center to let them know if, for example, (i) the patient may be heading for an undesired event, (ii) that the prescription should be changed, (iii) the drug may have to be changed based upon efficacy concerns, (iv) the patient tries early dispensing too many times (depends on the drug type, e.g., opioids), (iv) appears to be following an abuse pattern, etc., (v) is not following prescribing guidelines, and (vi) is failing to take the medication, etc.
  • the drug type e.g., opioids
  • the App allows the patient to ask certain questions regarding when they took their last medication (or medications for multidrug dispensers), how much medication is left, when their next dose is due, the medications expiration date, and the drugs package insert information, etc. It further provides access to personalized analytical charts, some which may be downloaded from the integrated support center's servers or created by the App from the limited information stored by the App, to show how the patient's symptoms are affected when the patient takes a drug dose. This is designed to aid in patient prescription persistence and assist in reinforcing the importance of prescription compliance.
  • the integrated support center IT system stores authorized log on information, all App history data and enables the continual update of the App history on all the patient's devices where the App has been downloaded.
  • the centralized servers are also designed to: (i) update individual App software as required, (ii) exchange information with authorized electronic medical records, (iii) to, on a real time basis, update the call center's disease management patient specific counselor screens, (iv) conduct metadata analysis on both the patient's individual data as well as analysis that may include information from the patient's electronic medical record, (v) carry out comparative patient analysis against metadata across a patient population with similar characteristics, etc.
  • the analytical output is designed to assist the call center's disease management group in its counseling of the individual patient as well as any reporting and contacts with the patient's prescribing medical professional.
  • the call center IT systems are designed to allow the call center, via the patient's drug specific App, (i) to change a patient's prescription based on an authorized prescriber's instructions, (ii) to lock and unlock the dispensing ability on the individual drug dispensing unit based upon a discussion with the patient and/or his care giver, and (iii) to lock all appropriate dispensing devices that contain a recalled drug and to instruct the patient via email and/or voice messages to go to their pharmacy to get the drug replaced or to follow the recalling manufacturer's instructions.
  • the call center's disease management team uses metadata analysis as well as drug registry information, as requested by the prescribing medical profession, to assist them in developing the best course of therapy based on specific queries of the integrated support center's databases and any authorized related electronic medical records.
  • FIG. 1 is an exemplary embodiment of a closed loop system controlled by a Drug Specific Dispensing Algorithm.
  • FIG. 2 is an exemplary embodiment showing a Drug Specific App which controls the Drug Dispensing Unit.
  • FIG. 3 is an exemplary embodiment of a Biometric Authentication screen.
  • FIG. 4 is an exemplary embodiment of Patient Self-Assessment Screens.
  • FIG. 5 is an exemplary embodiment of digitally available patient related diagnostic and physiological information.
  • FIG. 6 is an exemplary embodiment of a flow chart/decision tree used by the Drug Dispensing Algorithm.
  • FIGS. 7A and 7B are an exemplary embodiment of a flow chart of a standard prescription log in, Patient Self-Assessment and drug dispensing control.
  • FIGS. 8A-8D are an exemplary embodiment of the flow chart of the respective screens utilized to capture clinical trial data and to control the drug dispensing.
  • FIG. 9 is an exemplary embodiment of a Drug Dispenser.
  • FIG. 10 is an exemplary embodiment of a Drug Cassette.
  • FIG. 11 is an exemplary embodiment of Patient Self-Assessment Reporting Screens.
  • FIG. 12 is an exemplary embodiment of the Consolidated Therapy App and various Multi-Drug Dispensing devices.
  • FIG. 13 is an exemplary embodiment of the Centralized IT System.
  • FIG. 14 is an exemplary embodiment of an Integrated Support Center.
  • FIG. 15 is an exemplary embodiment of the design for a single drug Drug Dispenser.
  • FIG. 16 is an exemplary embodiment of how the Drug Dispenser's clam shell design is assembled for secure closing and opening.
  • FIG. 17 is an exemplary embodiment of the electronic schematic for the Drug Dispenser.
  • FIG. 18 is an exemplary embodiment of the placement of electronics and mechanical components on the outside and within the Drug Dispenser.
  • AKA denotes terms used interchangeably:
  • Adverse Event refers to (i) a medical occurrence temporally associated with the use of a medicinal product, but not necessarily causally related, (ii) any response to a drug which is noxious and unintended, and which occurs at doses normally used in man for the prophylaxis, diagnosis, or therapy of disease, or for the modifications of physiological function, (iii) an unexpected reaction not consistent with applicable product information or characteristics of the drug, and (iv) the unintended effect occurring at normal dose related to the pharmacological properties of a medication, etc.
  • Biometric Authentication (AKA biometric identification and biometric authentication.)
  • the definition encompasses but is not limited to biometric technologies that digitally capture fingerprint, palm and full-hand scanners, voice, facial recognition systems, iris scanning technology, document readers, biometric software, and related services capable of wireless, mobile or stationary use to limit access to the Patient.
  • biometric technologies that digitally capture fingerprint, palm and full-hand scanners, voice, facial recognition systems, iris scanning technology, document readers, biometric software, and related services capable of wireless, mobile or stationary use to limit access to the Patient.
  • the term also incorporates any system, while not biometric, that allows access via the use of a Login Name in combination with a Password and/or any additional security information.
  • AKA multiunit dispenser App is an App designed to recognize other Drug Specific Apps resident on an Interface Device and then to consolidate the requisite Patient Self-Assessment screens into a single interface for the control and dispensing of multiple drugs.
  • Digitally Captured refers to Patient data captured by diagnostic or monitoring devices and stored in a machine readable format.
  • Dispensing Device refers to the Drug Dispensing Unit with a Docked Drug Cassette whose dispensing is controlled by a Drug Specific App.
  • Dispensing System is comprised of the Dispensing Device and the Integrated Support Center.
  • Drug Cassette is the disposable unit that contains a Drug to be dispensed over a defined period of time and/or days per the prescription instructions.
  • Drug Dispensing Unit is the device where the Drug Cassette is Docked and whose dispensing mechanism (lock, unlock, and dispensing) are controlled by a Drug Specific App.
  • Drug Specific App refers to an app that requires Biometric Authentication prior to a Patient being able to respond to Patient Self-Assessment screens which are used by the App's Drug Specific Dispensing Algorithm to decide whether or not to signal the Dispensing Device to dispense the medication or to indicate to the patient and/or Integrated Support Center why the drug will not be dispensed.
  • Drug Specific Dispensing Algorithm refers to the decision tree based algorithm specifically develop for each drug to ascertain if the drug should or should not be dispensed.
  • AKA EMR Electronic Medical Record
  • PMR Patient Medical Record
  • Encryption (AKA Encrypted, Encrypted communications) is the most effective way to achieve data security. Access requires a secret key or password that enables decryption. Unencrypted data is called plain text; encrypted data is referred to as cipher text.
  • Expiration Date refers to the date after which a medication should not be taken.
  • AKA Digital Handshake refers to an exchange of signals between devices ensuring synchronization whenever a connection, as with another device, is initially established.
  • Integrated Support Center refers to a call center designed to provide patient support, disease management services and/or Dispensing Device support for patients, Prescribers, and/or payers.
  • Interface Device refers to the device (standalone drug delivery device, smart phone, tablet, computer, etc. with Internet communications capabilities) where the Drug Specific App resides.
  • Locked indicates the drug cannot be dispensed by the Dispensing Device until the Drug Specific App unlocks the Dispensing Device.
  • AKA structural metadata and descriptive metadata refers to the use of the organization of patient data to enable analysis of both individual and patient population data to ascertain how to best manage medication therapy on a drug by drug and patient by patient basis.
  • Patient refers to the individual that is prescribed and is taking a medication or medications. Examples include physicians, physician assistants, nurse practitioners, nurses, pharmacists, etc.
  • AKA patient-reported outcome or PRO covers a whole range of potential types of measurement self-reported by the patient. Each self-assessment scale or question measures a single underlying characteristic(s).
  • Prescriber is defined as any healthcare professional authorized by an individual country to write a prescription for a drug.
  • Recall refers to a drug recall issued by the manufacturer or a regulatory agency indicating that a particular drug batch or drug should not be taken.
  • Tamper Resistant refers to a design that makes it difficult to change, open, remove the cassette, or cause damage to the unit by anyone but authorized persons.
  • the invention and its various embodiments can enable the personalization of drug therapy, improve each drugs safety profile, ensure the continued efficacy of a drug for each patient, improve the quality of care, improve the patients quality of life by ensuring proper prescribing and prescription compliance, by promoting prescription persistence, and thereby decreasing the number of drug related medical interventions, and disease related physician visits and hospitalizations thereby decreasing the total cost of patient care.
  • This Invention in its various embodiments is applicable to and by reference incorporates the drugs, drug mechanisms of action, and diseases listed in Table 1-Table 8.
  • Table 1 lists oral drugs with REMS programs.
  • the listed approved drugs are encompassed in the embodiment of the invention by reference can benefit from an improved drug safety profile.
  • the Invention mitigates prescription risk for the drug manufacturer and prescriber as it shifts the responsibility to the patient.
  • the listing for each drug includes by definition each drug's respective indication(s), strength, dosage form, route of administration, side effect profile, drug interactions, etc.).
  • the embodiment incorporates by reference the Food and Drug Administration's (FDA) Approved Risk Evaluation and Mitigation Strategies (REMS) drugs listing.
  • FDA Food and Drug Administration's
  • REMS Approved Risk Evaluation and Mitigation Strategies
  • Benzodiazepines Like Klonopin (clonazepam) Valium (diazepam) Xanax (alprazolam)
  • Non-Benzodiazepines Like Ambien (zolpidem) Lunesta (eszopiclone) Sonata (zaleplon) Others Chantix Revlimid Tracler Xeljans (Jak Compounds)
  • Table 2 lists the Paragraph IV Challenged Drugs that can benefit from the increased patent protection afforded by the drug/device (Invention) combination.
  • the listing for each drug includes by definition each drug's respective indication(s), strength, dosage form, route of administration, side effect profile, drug interactions, etc.
  • Table 3 Marketed Drugs lists approved drugs which are encompassed in the embodiment of the invention by reference. Drug compounds of interest are also listed in: Goodman & Gilman's, The Pharmacological Basis of Therapeutics (12th Ed) (Goodman et al. eds) (McGraw-Hill) (2011); and 2015 Physician's Desk Reference which are also encompassed in the embodiment of the invention by reference.
  • the listing for each drug includes by definition each drug's respective indication(s), strength, dosage form, route of administration, side effect profile, drug interactions, etc.
  • Cipro ciprofloxacin HCI tablets Clarinex Clarithromycin (Biaxin) Claritin RediTabs (10 mg loratadine rapidly-disintegrating tablet) Claritin Syrup (loratadine) Claritin-D 24 Hour Extended Release Tablets (10 mg loratadine, 240 mg pseudoephedrine sulfate) Clemastine fumarate syrup Cleocin (clindamycin phosphate) Cleviprex (clevidipine) Climara Clindamycin phosphate topical gel Clindamycin Phosphate Topical Solution USP 1% Clolar (clofarabine) Clomipramine hydrochloride Clonazepam Coartem (artemether/lumefantrine) Colazal (balsalazide disodium) Colcrys (colchicine) Combivir Cometriq (cabozantinib) Complera (emtricitabine/rilpivirine/tenofovir dis
  • Synjardy (empagliflozin and metformin hydrochloride) Synribo (omacetaxine mepesuccinate) Synthroid (levothyroxine sodium) Synvisc, Synvisc-One (Hylan GF 20) Tafinlar (dabrafenib) Tamiflu capsule Tanzeum (albiglutide) Tarceva (erlotinib, OSI 774) Targiniq ER (oxycodone hydrochloride + naloxone hydrochloride) extended-release tablets Tasigna (nilotinib hydrochloride monohydrate) Tasmar Tavist (clemastine fumarate) Taxol Taxotere (Docetaxel) Tazorac topical gel Tecfidera (dimethyl fumarate) Technivie, (ombitasvir, paritaprevir and ritonavir) Teczem (enalapril maleate/diltiazem malate) Tefl
  • Table 4 lists sample drugs and their side effects.
  • the listed drugs and their side effects highlight a number side effects that can be used for the development of the Patient Specific Dispensing Algorithm.
  • the following approved drugs in Table 4 and in the following marketed drug compounds and drug compounds in development are encompassed in the embodiment of the invention by reference.
  • Marketed drug compounds of interest are also listed in: Goodman & Gilman's, The Pharmacological Basis of Therapeutics (12th Ed) (Goodman et al. eds) (McGraw-Hill) (2011); and 2015 Physician's Desk Reference.
  • Drug compounds in development that are of interest are also listed in: CortellisTM Competitive Intelligence by Thomson Reuters; Adis R&D; and Pharmaprojects by Citeline.
  • the drug The listing for each drug includes by definition each drug's respective indication(s), strength, dosage form, route of administration, side effect profile, drug interactions, etc.
  • Cardiovascular Hypertension (tumors, 4% to 13%; kidney transplant, 30%; liver transplant, 17%), Peripheral edema (tumors, 13% to 39%; kidney transplant, 45%; liver transplant, 18%)
  • Dermatologic Acne (tumors, 10% to 22%; transplant, 1% to less than 10%)
  • Eczema renal angiomyolipoma, 10%
  • Rash tumors, 5% to 59%)
  • Endocrine metabolic Dyslipidemia (kidney transplant, 15%), Hypercholesterolemia (tumors, 66% to 85%; kidney transplant, 17%), Hyperlipidemia (kidney transplant, 21%; liver transplant, 24%), Hypertriglyceridemia (tumors, 27% to 73%), Hypoalbuminemia (breast cancer, 33%), Hypophosphatemia (tumors, 9% to 49%; kidney transplant, 13%), Increased glucose level
  • Table 5 is included by reference as the drugs that are listed as in development in the following databases: CortellisTM Competitive Intelligence by Thomson Reuters; Adis R&D; and Pharmaprojects by Citeline.
  • the drugs in the development pipeline can utilize the Invention to capture required clinical trial information and control drug dispensing for regulatory drug approval as well as to control drug dispensing after regulatory approval.
  • the drugs are encompassed in the embodiment of the invention by reference.
  • the listing for each drug includes by definition each drug's respective indication(s), strength, dosage form, route of administration, side effect profile, drug interactions, etc.
  • Table 6 is included by reference as the mechanisms of action for marketed drugs, drugs in developed, and efficacious drugs whose development was stopped due to a side effect(s) that can be addressed by the embodiment and thereby made approvable.
  • the listed drugs in the following databases are encompassed in the embodiment of the invention by reference: CortellisTM Competitive Intelligence by Thomson Reuters; Adis R&D; and Pharmaprojects by Citeline.
  • the listing for each includes by definition each respective drug's respective indication(s), strength, dosage form, route of administration, side effect profile, drug interactions, etc.
  • Table 7 is included by reference as the oral drugs listed in the following databases that (i) were in development but were disconintued due to dose related side effects whose safety concerns can be addressed by the Invention or (ii) drugs that were withdrawn from the market after approval due to dose related side effects whose safety concerns can be addressed by the Invention: CortellisTM Competitive Intelligence by Thomson Reuters; Adis R&D; and Pharmaprojects by Citeline. These drugs are encompassed in the embodiment of the invention by reference.
  • the listing for each drug includes by definition each drug's respective indication(s), strength, dosage form, route of administration, side effect profile, drug interactions, etc.
  • Table 8 is a sample list of diseases encompassed in the embodiment of the invention by reference.
  • the listing for each encompasses drugs used to treat the disease and for each includes by definition each drug's respective indication(s), strength, dosage form, route of administration, side effect profile, drug interactions, etc.
  • Aortic Aneurysm see Aortic Aneurysm ACE (Adverse Childhood Experiences) Acinetobacter Infection Acquired Immune Deficiency Syndrome (AIDS) - see HIV/AIDS Acquired Immunodeficiency Syndrome (AIDS) - see HIV/AIDS Adenovirus Infection Adenovirus Vaccination ADHD [Attention Deficit/Hyperactivity Disorder] Adult Vaccinations Adverse Childhood Experiences (ACE) African Trypanosomiasis - see Sleeping Sickness Agricultural Safety - see Farm Worker Injuries AHF (Alkhurma hemorrhagic fever) AIDS (Acquired Immune Deficiency Syndrome) AIDS (Acquired Immunodeficiency Syndrome) Alkhurma hemorrhagic fever (AHF) ALS [Amyotrophic Lateral Sclerosis] Alzheimer's Disease Amebiasis, Intestinal [ Entamoeba histolytica infection] American Indian and Alaska
  • EHDI Early Hearing Detection and Intervention
  • EEE Ebola Virus Disease
  • EBV Infection Epstein-Barr Virus Infection
  • Echinococcosis EEE (Eastern Equine Encephalitis)
  • EHDI Early Hearing Detection and Intervention
  • Ehrlichiosis Human Elephantiasis - see Lymphatic Filariasis Emerging Infectious Diseases Entamoeba histolytica infection - see Amebiasis, Intestinal Enteric Diseases from Animals - see Gastrointestinal Diseases from Animals Enterobius vermicularis Infection - see Pinworm Infection Enterovirus D68 Enterovirus Infections (Non-Polio) - see Non-Polio Enterovirus Infections Epidemic Typhus - see Typhus Fe
  • Klebsiella pneumoniae Kala-Azar - see Leishmania Infection Kawasaki Syndrome (KS) Keratitis, Fungal - see Fungal Keratitis Kernicterus - see Newborn Jaundice KFD (Kyasanur Forest disease) Kidney Disease (CKD) Klebsiella pneumoniae ( K.
  • KS Leishmania Infection Kawasaki Syndrome
  • CKD Kidney Disease
  • FIG. 1 illustrates an exemplary embodiment of the present invention, an integrated drug dispensing and disease management system composed of a Drug Specific App 10 which contains a Drug Specific Dispensing Algorithm 15 resident on an Interface Device (Smart Phone, computer Tablet, portable or desktop computer, standalone drug dispenser, etc. with Internet communications capabilities) 20 used to control dispensing by a (single or multidrug) Drug Dispenser 30 ; an Integrated Support Center 40 ; a Patient 50 ; a Prescriber 60 ; and the Patient's Electronic Medical Record 70 .
  • a Drug Specific App 10 which contains a Drug Specific Dispensing Algorithm 15 resident on an Interface Device (Smart Phone, computer Tablet, portable or desktop computer, standalone drug dispenser, etc. with Internet communications capabilities) 20 used to control dispensing by a (single or multidrug) Drug Dispenser 30 ; an Integrated Support Center 40 ; a Patient 50 ; a Prescriber 60 ; and the Patient's Electronic Medical Record 70 .
  • a Drug Specific App 10 which contains a
  • FIG. 2 is an exemplary embodiment depicting a Drug Specific Dispensing App 80 which resides on an Interface Device 20 and controls drug dispensing.
  • the Patient 50 is prescribed a Drug
  • the Patient 50 is trained on the operation of the Drug Specific Dispensing App 80 and the related Drug Dispenser 30 using the Apps training interface.
  • the Drug Specific App 80 is comprised of the following software modules: (i) Biometric Authentication 80 a , (ii) Prescription 80 b module which can be programmed remotely by the Integrated Support Center 40 , (iii) Patient Reminder 80 c , (iv) Interface Device 80 d , (v) Patient Self-Assessment 80 e module which is unique for each drug, (vi) Digital Capture (APIs) 80 f , (vii) the Drug Specific Dispensing Algorithm 80 g which is unique for each drug, (viii) Dispensing Communication and Reporting 80 h , (ix) the Integrated Support Center 80 i , (x) the Patient Reporting 80 j , and (xi) the App and Dispensing Unit Operation Training Interface 80 k.
  • Biometric Authentication module 80 a encompasses the utilization of a biometric authentication screen and/or digital interface which allows the patient, upon authentication, to automatically move to the Patient Self-Assessment screens 100 , 102 , 104 if: (i) the authentication routine recognizes the Drug Dispenser's 30 serial number to be one that was registered to the Patient 50 , (ii) digitally Handshake with the Drug Specific App 10 and (iii) the Biometric Authentication 80 a recognizes the Patient 50 . If the Biometric Authentication 80 a does not recognize the Patient 50 , it asks the Patient 50 to try again.
  • the App 50 After a given number of tries, it alerts the patient to talk with the Integrated Support Center 40 and alerts the Integrated Support Center 40 of the failed attempts and lists the Patient 50 for a follow-up call if the drug has not been properly dispensed within a drug specific timeframe. If the App 50 does not recognize the Drug Dispenser 30 , the patient gets an alert screen explaining why it does not recognize the dispenser, this may include but is not limited to: (i) unable to locate the Drug Dispenser 30 , (ii) the Drug Dispenser 30 does not have the right serial number, etc.
  • the App 10 senses that the Drug Dispenser does not have the right serial number, it will send a message to the Integrated Support Center 40 indicating the serial number of the recognized Drug Dispenser for follow-up action by the Integrated Support Center 40 .
  • One alternative for the Integrated Support Center 40 is to lock the App screen to only give the Patient 50 the choice of calling the Integrated Support Center 40 to resolve his dispensing issue.
  • the Prescription module 80 b which is unique to the drug, encompasses the ability of the Prescriber 60 , other authorized healthcare professionals, or the Integrated Support Center 40 to input the prescribing information into the Drug Specific App 10 .
  • the person entering the prescription information begins by entering the drugs Brand and/or generic name, strength/dosage, NCD number, Batch Number, any pertinent required contact information in case of an overdose or emergency, and the drug's expiration date. This input can be done manually and/or via a barcode scan of the Individualized Drug Cassette 170 .
  • the prescribing information defines the dosing strength and administration schedule (e.g, q.d., b.i.d., t.i.d., q.i.d., q.h.s., ⁇ X a day, ⁇ X per week, ⁇ X per month, q.4h, q.6h, q.o.d., a.c., p.c., prn, etc.).
  • the prn dosing, and/or for example the patient self-analgesia dosing can be designated to allow the Patient 50 to self-medicate using multiple smaller doses to a maximum cumulative dose over a specified period of time. Once the maximum does is dispensed, the Drug Dispenser is locked by the Drug Specific App 10 until the next dosing period begins and the patient enters the requisite information to enable the Drug Specific App 10 to signal the Drug Dispenser to dispense.
  • the Patient Reminder module 80 c encompasses the ability of the Drug Specific App 10 to alert the Patient 50 using different methodologies including but not limited to: (i) initiating a phone call, (ii) buzzing the device, (iii) sending an email message, (iv) sending a text message, and/or (v) having the Integrated Support Center 40 call the Patient 50 , etc.
  • the Drug Specific App 10 When the phone call is initiated, the Drug Specific App 10 is shown on the Smart Phone's screen. When the phone is turned on or unlocked, the screen automatically moves to the Biometric Authentication 90 screen. If the Drug Specific App 10 is clicked on a Smart Phone, it opens to the Biometric Authentications 90 screen.
  • the Interface Device module 80 d encompasses many functions: (i) home for the Drug Specific App 10 , (ii) enables the Drug Specific App 10 to utilize the Interface Device features to facilitate the Drug Specific App's interface with the Patient 50 , (iii) uses the Interface Device's 20 Wi-Fi communications capability to interface with the Drug Dispenser 30 and its Internet communications capability to interface with the Integrated Support Center 40 , (iv) uses the phone to call the Integrated Support Center 40 , and utilizes the Interface Device's 20 memory to store the prescription, dispensing history, and the Patient Self-Assessment (see illustrative examples in FIG. 4 ) and digital (see representative examples under FIG. 5 ) physiological, psychological, lifestyle, currently taken medications, and environmental data.
  • the Patient 50 is, for example, able to utilize the Interface Device's 20 navigation capabilities to move between screens and to correct prior inputs before exiting by selecting the dispense or exit buttons.
  • Interface Device's 20 GPS device Utilizes the Interface Device's 20 GPS device to capture the location when the medication is dispensed.
  • Patient Self-Assessment module 80 e is specific for each drug based upon, for example, the drug's side effects, potential drug interactions, implications of under and/or overdosing, efficacy measures, dosing schedule, drug strength, single or multidrug regimen, effects of weight gain, aging, development of comorbidities, etc.
  • Certain Patient Self-Assessment 100 , 102 , 104 screens will, for example, incorporate known self-assessment scales or will incorporate self-assessment screens specifically developed for the specific drug. The screens may also be those which are designed to capture Patient specific information required by regulatory agencies for the subsequent approval of the drug and/or for post marketing studies.
  • the Digital Capture (APIs) module 80 f encompasses, as an exemplary, digital information that is integrated via the Drug Specific App 10 via Digital Capture from, as examples, a wearable monitoring device 110 , a digital scale 112 , a third-party monitoring App on a smart phone 114 , a hand held diagnostic device 116 , a lifestyle monitor 117 , a digitalized home diagnostic or self-diagnostic 118 , a swallowed tracking and/or diagnostic aid, a drug tracking chip, radio frequency identification device (RFID), or care giver or parent patient assessments and/or journal entries, etc.
  • RFID radio frequency identification
  • the Drug Specific Dispensing Algorithm module 80 g encompasses, as an example, the Product Expiration 122 date, Properly Stored 123 information (for example, temperature, moisture, etc.), one or more Patient Self-Assessment 125 , 126 and/or one or more Digitally Captured 127 values, the Dispensing Algorithm 128 , the Dispense 129 command screen and interface with the Drug Dispenser 30 , and patient feedback and instruction screens 130 , 132 , 134 , 136 , 138 , 140 , 142 , 144 , 146 , 148 , 150 , 152 , etc.
  • the Dispensing Communications and Reporting 80 h module encompasses, for example, the interface between: (i) the Drug Specific App 10 and the Drug Dispenser 30 via the Interface Device 20 ; (ii) the interfaces between the Drug Specific App 10 and any proprietary or third-party digital devices, data aggregation devices, computer databases, diagnostic devices, and medication tracking devices, etc., for example, those digital devices listed under FIG.
  • the Integrated Support Center 80 i module encompasses, for example, (i) securely handshaking/connecting the Drug Specific App 10 to the Integrated Support Center 40 , (ii) sending to and receiving alerts from the Integrated Support Center 40 , (iii) enabling the Integrated Support Center 40 to lock or unlock the Drug Dispenser 30 , (iv) alert the Integrated Support Center 40 of unusual attempts to open the Drug Dispenser 30 , (v) the ability of the Integrated Support Center 40 to remotely update the Drug Specific App software, and (vi) enables the Drug Specific App 10 to access patient reports, charts, and graphs, (vii) enables the patient to require a refill prescription be sent to his/her pharmacy for refill, etc.
  • the Patient Reporting 80 j module encompasses, as an example: (i) an ability by the Patient 50 to request certain reports, e.g., the last time the Patient 50 took the medication, prescription information details, drug details (brand and generics names, batch number, expiration date, doses remaining, reorder information, drug interactions, typical side effects, etc.; (ii) graphs and charts created by the Drug Specific App 10 based upon Interface Device 20 stored information; (iii) graphs, charts and/or reports downloaded from the Integrated Support Center's servers, etc.
  • the App and Dispensing Unit Operation Training Module 80 k encompasses, as an example, (i) a hot link to a video library resident on the Integrated Support Center's servers, You Tube, and/or other consumer video services covering all aspects of utilizing the Drug Specific App 10 , using and troubleshooting the Drug Dispenser 30 , (ii) a step by step tutorial resident on the Interface Device 20 , (iii) a hot linked “help” button on each respective screen allowing the Patient 50 to bring up usage instructions for the respective screen without interrupting the sequence of entering the required prescription information or selecting a particular command, etc.
  • FIG. 3 The exemplary embodiment of the Biometric Authentication 90 interface encompasses a system that is compliant with the Health Insurance Portability and Accountability Act (HIPAA), which sets the standard for protecting sensitive patient data. This means that all the required physical, network, and process security measures are in place and followed and incorporated herein by reference.
  • HIPAA Health Insurance Portability and Accountability Act
  • FIG. 4 The exemplary embodiment of the Patient Self-Reporting Screens 100 , 102 , 104 encompass, for example, an abdominal pain self-reporting scale adapted from Wong Baker Faces 100 ; the stool consistency utilizes the Bristol Stool Scale, a well-accepted stool measure 102 ; and the current abdominal discomfort scale was developed by MMC International from the Defense and Veterans Pain Rating Scale 104 .
  • These are examples of patient self-reporting screens that can be utilized in the embodiment as an input to the Drug Specific Dispensing Algorithm 15 to decide whether or not to dispense.
  • the scales can be created, adapted, or integrated to capture the desired patient self-reported information. This can be, for example, for clinical trials, post marketing surveillance, and/or for incorporation into the Drug Specific Dispensing Algorithm 15 .
  • FIG. 5 The exemplary embodiment of the Digitally Captured information 110 , 112 , 114 , 116 , 117 , 118 is illustrative for the types of digital information which can be collected and integrated into the Decision Tree/logic in the respective Drug Specific Dispensing Algorithms 15 .
  • the availability of disease specific Apps and related disease or condition specific digitalized health information is rapidly emerging, making the examples in FIG. 5 wanting not only for the disease information but for lifestyle, medications being taken, digital medication diagnostic and tracking devices, and environmental input, etc.
  • FIG. 6 The exemplary embodiment of a Drug Specific Dispensing Algorithm 120 , 121 , 122 , 123 , 124 , 125 , 126 , 127 , 128 , 129 , 130 , 132 , 134 , 136 , 138 , 140 , 142 , 144 , 146 , 148 , 150 , 152 is illustrative of the Decision Tree, sequencing, and messaging that is utilized by each Drug Specific Dispensing Algorithm 15 .
  • Biometric Authorization 120 , 121 , Product Expiration 122 , and Properly Stored 123 are constant variables in the dispensing decision.
  • the respective messages are either standard, as an example those related to locking the Drug Dispenser 130 , 136 , 142 , 148 or Notify Call Center 132 , 138 , 144 , 150 , or Product Expired 132 , 134 or the drug was not Properly Stored 138 , 140 , etc. Screens indicating why a drug is not “Allowed to Dispense” are specifically adapted to the drug and report the reasons why the drug was not dispensed 144 , 146 . Each Drug Specific Dispensing Algorithm 15 is specifically developed to control the dispensing of a specific medication.
  • FIGS. 7A and 7B present the exemplary embodiment illustration of the Patient 50 interaction to dispense, as example, alosetron, a 5HT3 antagonist for the treatment of diarrhea predominant irritable bowel syndrome (IBS-D).
  • the process begins by the Drug Dispensing App 160 alerting the Patient 50 that it is time to take his/her medication. If it is on a smart phone, it also changes the screen to the Drug Dispenser App 160 graphic′ and when the Patient 50 unlocks the phone, the screen automatically changes to the Biometric Authentication screen 162 .
  • the Patient 50 can click on the Drug Dispensing App 160 for alosetron, this is automatically followed by a Biometric Authentication screen 162 , upon authentication, the screen automatically moves to the Patient Self-Assessment screens 164 , 166 , 168 , 170 . A click on a value of the self-assessment screen automatically moves the process to the next screen. If nothing is found to block dispensing by the alosetron Drug Specific Dispensing Algorithm 15 , then the Patient 15 sees the Dispense screen 172 .
  • Dispense By clicking on Dispense, the patient is then able to go to the related Drug Dispenser 30 and click, for example, on top of the dispenser to dispense a single dose—after which the Drug Dispenser goes back to a locked position. If the Patient 50 wants to change a prior entry before dispensing, he/she can use the devices scroll back capabilities to return to the right screen and change the selection. If the alosetron Drug Specific Dispensing Algorithm 15 finds any reason not to allow dispensing, it selects from the appropriate drug specific screen to show why dispensing was rejected and to facilitate the Patient's ability to avail himself/herself of the proper medication support 176 , 178 , 180 .
  • FIGS. 8A-8D are an exemplary embodiment of the alosetron Drug Specific App configured to capture all the Patient Self-Assessment information which is required by the FDA or EMA for the approval of a 5HT3 drug.
  • the only difference to FIGS. 7A and 7B are the additional input screens 200 , 202 , 204 , 208 , 210 , 212 , 214 required by the regulatory agencies.
  • the same Drug Specific Dispensing Algorithm 15 , decision tree, would be used for the clinical trial configuration as for the alosetron example in FIGS. 7A and 7B .
  • the embodiment is applicable for, as an example, clinical trials, post-launch surveillance, for the FDA's Risk Evaluation and Mitigation Strategy (REMS) programs, and to control and ensure drugs are efficacious and safe as dispensed within the Drug Specific Dispensing Algorithm 15 as part of a prescribed drug regimen, etc.
  • FDA's Risk Evaluation and Mitigation Strategy FDA's Risk Evaluation and Mitigation Strategy
  • FIG. 9 is an exemplary embodiment illustration of the Drug Dispenser 230 , 232 , 234 designed to be: (i) controlled by a Drug Specific App 10 resident on an Interface Device 20 , (ii) water proof, (iii) tamper resistant, (iv) withstand being dropped and/or banged, to be rugged, (v) operate and withstand hot and cold temperatures within defined temperature ranges, (vi) reusable, (vii) rechargeable, and (viii) small enough to be carried in a pants pocket or purse.
  • the Drug Dispenser 230 automatically recognizes the drug based upon the Drug Specific Drug Cassette 240 docked into the device.
  • the Drug Specific Drug Cassette 240 can only be docked or removed by a healthcare professional.
  • the Drug Dispenser 230 remains locked from dispensing unless it receives an encrypted signal from the authorized Drug Specific App 10 .
  • the Drug Dispenser 230 dispenses the drug with one click.
  • the Drug Dispenser 230 when interfaced through a digital handshake with the drug specific App transmits for example: (i) its serial number, (ii) the drug information on the Drug Specific Drug Cassette 240 , (iii) current and historic temperatures since the last dispense, (iv) humidity exposure since the last dispense, and (iv) the date and time the drug was last dispensed.
  • FIG. 10 is an exemplary embodiment illustration of the Drug Specific Drug Cassette 240 designed: (i) to use approved drug packaging materials, (ii) to dock into the Drug Dispenser 242 , 244 , and (iii) as a blank cartridge which can accommodate a number of different pills, caplets, capsules, etc. within a specified size range.
  • the blank Drug Specific Drug Cassette 240 is designed to be proprietary to the Drug Dispenser 230 and is marked, as part of the automated cassette fill operation, to allow the Drug Dispenser 230 to ascertain the: (i) name of the drug (brand and/or generic), (ii) drug's NDC number, (iii) drug batch number, (iv) drug's expiration date, etc.
  • the cassette closure is designed to allow printing or any required regulatory information.
  • FIG. 11 presents exemplary embodiment of the Patient 50 specific charts 250 , 252 , 254 which illustrate the relationship between when the Patient 50 took their medication versus his/her self-assessment or digitally captured symptoms and/or diagnostic values. This clearly shows the relationship between the medication and symptoms.
  • the charts or tables, which can be requested and viewed by the Patient 50 on the Interface Device 20 are designed to educate the patient and promote Patient 50 prescription compliance and persistence.
  • Prescribers 60 can utilize the information to ensure the medication is efficacious for the individual Patient 50 , to titrate dosing, and to personalize drug therapy (for personalized medicine).
  • the respective charts, graphs, reports, etc. may be generated by the Drug Specific App 10 and/or by the Integrated Support Centers 40 centralized analytics platform.
  • FIG. 12 is an exemplary embodiment illustration of Drug Dispensers designed to serve the needs of most Patients 50 . Approximately half of all Patients 50 take two medications and 20 percent take five or more. Consolidated Therapy App 270 automatically senses other Drug Specific Apps 10 that or on the Interface Device 20 . It consolidates from two to many Drug Specific Apps 10 into a single user interface for all drugs—eliminating duplicate logins, entries, and record keeping. It in turn digitally handshakes with the Multi-Drug Dispenser 280 and uses the individual Drug Specific Dispensing Algorithms to control dispensing of each individual medication. Furthermore, it coordinates the dispensing schedules to have as few dispensing times, within the respective prescriptions, as possible. Multi-Drug Dispenser eliminates concerns about which drugs have to be taken when.
  • Illustrations 282 , 284 , 286 , and 288 are exemplary of dispensing units containing from two drugs to five drugs. These units are standalone or can be docked into a Multi-Dispenser desktop unit.
  • FIG. 13 is an exemplary embodiment of the Drug Dispenser 292 and the Drug Specific App 294 interfaces with the: (i) centralized Servers, (ii) databases, and (iii) Analytics systems (the IT System 290 ), through the Interface Device 294 e , to ensure the Patient 304 is receiving the best care, tailored to the Patient (“personalized medicine”), for the prescribed Drug.
  • All the data collected by the Drug Specific App 294 , from the Drug Dispenser 292 , Digitally Captured Information 294 a , 294 b , 294 c , the Patient Self-Assessment screens 100 , 102 , 104 contained within the Drug Specific App 294 , and the respective output of the Drug Specific Dispensing Algorithm 15 are transmitted by the Drug Specific App 294 through the Interface Device 294 e to the appropriate Patient database on the centralized Servers 290 .
  • the data is utilized to update the respective patient screens used by the Disease Management Counselors in the Integrated Support Center.
  • the data is also made available to the respective Drug Registries 306 and the related Electronic Medical Record 296 . Any information that requires a communication with the Patient 304 and/or the Prescriber 308 is handled either automatically by the patient management software or by the Integrated Support Center 302 .
  • the patient's information is continually analyzed by the analytical routines both individually for the patient as well as in comparison with treatment data from other like patients to ascertain if any changes in therapy may be warranted.
  • This analytical capability is utilized by the Integrated Support Center 302 to assist Prescribers 308 when they are trying to develop a treatment plan for difficult patients.
  • the Analytics 290 performed may include the patient's data, pooled patient information, as well as information from Electronic Medical Records 296 , clinical studies, and publications, etc.
  • the centralized Servers and Analytics 290 provide the following, as well as other, exemplary backbone support:
  • For the Drug Specific App 294 (i) assigns the App to a specific Patient 304 , (ii) links the Drug Dispenser 292 to the Drug Specific App 294 which in turn limits the dispenser and App only to work with one another, (iii) stores the App codes on server, and (iv) enables and updates the Drug Specific App software via communication with the Interface Device 294 e , etc.
  • For the Drug Dispenser 292 (i) stores all reported data in the designated databases on the Servers 290 , (ii) syncs the patient data on all the respective Interface Devices 294 e ; (iii) stores dispensing, dispensing attempts, lock, and malfunction data; (iv) transmits reports to patient via the Drug Specific App 294 on request; (v) enables lock or unlock transmission from the Integrated Support Center 302 ; changes the Drug prescription on the Drug Specific App 294 as imputed by the Disease Management Represented per the Prescribers 308 instructions, and (vi) stores the authorized medical professional identification code required for the professional to open the Drug Dispenser 292 in order to change or load the Drug Specific Drug Cassette 242 , etc.
  • Integrated Support Center 302 For the Integrated Support Center 302 : (i) aggregate patient data, (ii) presents and updates data on patient specific Managed Care call center screens, (iii) provides the ability to change a Patient's 304 prescription, (iv) enables the remote locking and unlocking of individual Drug Dispensers 292 via their Drug Specific App, (v) enable drug specific transmissions to all Patients 304 , (vi) enables simultaneously locking all Drug Dispenser 292 for a specific Drug in the event of a Drug recall, and enables medical professionals to open, load, and close the Drug Dispenser 292 , etc.
  • Registries 306 For Registries 306 : (i) maintains the Registry 306 , Electronic Medical Record 296 and App databases and analytics. (ii) prepares Therapy efficacy reports, (iii) prepares best practices reports, and (iv) through the Integrated Support Center provides Patient 304 specific diagnosis and therapy assistance to Prescribers 308 as requested.
  • Prescriber 308 (i) prepares and sends Patient 304 alerts, (ii) conducts meta-data analysis, prepares Patient specific reports and shares the results with the Prescriber 308 , (iii) provides the Prescriber 308 , through the Integrated Support Center 302 , assistance/guidance based upon Prescriber 308 requested database and analytics queries, and (iv) prepares best practices reports based upon patient and Electronic Medical Records 296 meta-data analysis, etc.
  • FIG. 14 is an exemplary embodiment illustration of how the Integrated Support Center 310 interfaces with the Drug Specific App 312 , the Patient 314 , the Prescriber 318 , and the Electronic Medical Record 316 .
  • the Integrated Support Center's 310 interactions with the Patient 314 can be instigated by a number of different scenarios and take on many different forms. Examples include but are not limited to: (i) receipt of a patient alert from the Patient's Drug Specific Drug App 312 ; (ii) Patient 314 calls; (iii) answering Patient 314 questions about the device, App, the drug, or their therapy; (iv) Patient 314 counseling within the support center's guidelines; (v) locking the individual patient's Drug Dispenser 30 based upon: (a) an Drug Specific App alert, (b) an Integrated Support Center Analytics alert, (c) a patient conversation, etc.; (vi) unlocking the individual patient's Drug Dispenser 30 based upon: (a) a conversation with the Patient 314 , (b) a conversation with the Prescriber 318 , etc.
  • the Integrated Support Center 310 provides: (i) “Compliance” and “Adherence” support; (ii) outbound patient telephone calls; (iii) patient monitoring; (iv) emails and/or calls the patient's physician to recommend therapy change, etc.; (v) patient disease management education; (vi) ensures patient has access to their drug; (vii) as required, works with payers to obtain coverage for high cost medications; (viii) looks for prescription financial assistance programs; (ix) patient education and reeducation; (x) patient follow-up, and (xi) Medical Affairs support.
  • the Integrated Support Center's 310 interactions with the Prescriber 318 can be instigated by a number of different scenarios and take on many different forms. Examples include but are not limited to: (i) locking or unlocking a specific patient's Drug Dispenser 30 ; (ii) changing the prescription; (iii) patient specific physician support using the Integrated Support Center's 310 Analytics 290 to ascertain patient specific treatment alternatives; (iv) assist with patient specific data analysis; (v) provide disease/condition specific information; and (vi) Medical Affairs support, etc.
  • FIG. 15 illustrates an exemplary embodiment of the design of a single drug Drug Dispenser 324 .
  • the size of said dispenser 324 in the exemplary being 3.8 inches tall by 2.5 inches wide by 9/16 th inches wide.
  • the design incorporates a clam shell design 320 , 330 with a pivot on one corner and a tamper resistant and waterproof seal on the opposite edge right before the corner. All design work meets the respective FDA 21 CFR 820 Quality System Regulation, design center ISO 13485:2003 certification and Risk Management process for design, ISO14971, requirements.
  • the Drug Dispenser 320 , 322 , 324 , 326 , 328 , 330 has been designed for manufacturing (on both PCB and plastics or sheet metal parts), assembly (PCBA and Box Build), and cost.
  • the design incorporates failure modes and effects analysis (FMEA) to address all possible failures in design, manufacturing, assembly, interface with the Drug Specific App 10 or when used by a patient. It is designed for testing, continual design improvement, the environment, and
  • FIG. 16 is an exemplary embodiment illustration of the assembly and locking mechanism for the Drug Dispenser's 332 clamshell design.
  • the interior of the top of the clamshell 334 incorporates hinges that marry with the hinges on the inside of the bottom clamshell interior 338 . These are locked together with a hinge pin 336 that is treaded through the holes in the respective hinges, much the same as the hinges are held together on most common entry doors.
  • top 334 and bottom 348 clamshells are locked closed and together by use of a microactuator moved locking bar 342 .
  • the locking bar is pulled down by the microactuator and the hook's male member docks into the the female orifice on the locking buttoms 344 .
  • the design incorporates integrated supports 354 to ensure the intergrity and durability of the design. They are also instrumental in addind strength, as required, for adding anchors for the respecitive Drug Dispenser 332 components.
  • the design eliminates the ability to open the Drug Dispenser without an authorized signal to cause the microactuator to unlock 342 .
  • the Top Cap 340 is fitted to close the top of the Bottom Clamshell.
  • the top of the Top Cap 340 covers the top of the Hinge Pin 336 and holds it in place.
  • the Bottom Cap 350 covers the bottom of the Hinge Pin 336 and holds it in place.
  • the right interior to the Top Cap provides for a dock for the end of the Lock Bar 342 and allows it to move up and down, to lock or unlock, as required.
  • the Bottom Cap 350 provides the seat that supports the Microacturator 342 that lock and unlocks the clamshell by moving the Lock Bar 342 up and down.
  • the Top 340 and Bottom 350 Caps are secured to the Bottom Clamshell Interior 348 by screws that securely marry each of the pieces together.
  • the unit then forms a ridged platform for the Top Clamshell Interior 334 to dock with.
  • the Drug Dispenser 332 When the Drug Dispenser 332 is closed, it forms a sturdy, tamper resistant housing for the Drug Specific Drug Cassette 240 .
  • the Drug Dispenser 332 has a Clasp Lock 346 designed to exert the desired level of pressure on the closing joints to secure design integrity.
  • the Top Cap 338 incorporate the one click dispensing button.
  • the Bottom Cap 352 houses the dispensing port.
  • FIG. 17 is an exemplary embodiment of the Drug Dispenser's 324 electronics and features schematic.
  • the Drug Dispenser's 324 system is comprised of an Applications Processor 368 that contains the units Firmware, individual Drug Dispenser 324 serial number, and manages all functions.
  • the main unit components are the: (i) communications connectivity 362 module, (ii) its data transfer capability 366 , (iii) the units sensors and/or applications 364 that allow the unit to authenticate the user, sense efforts to tamper/open the unit without authority, measure drug storage temperature and humidity, to time time stamp an action or event (clock function), and locate the unit via GPS; (iv) the display module 370 ; (v) the Power Management and recharge system 376 ; (vi) Memory management 374 ; (vii) Cassette Controller which rotates the Drug Specific Drug Cassette 240 which enables dispensing as well as the unit to read specific drug cassette information; (viii) the Dosage Dispenser system 372 ; and (ix) the various components designed to facilitate and protect the different system functions.
  • FIG. 18 is an exemplary embodiment of the placement of electronics and mechanical components on the outside and within the Drug Dispenser.
  • the front of the Drug Dispenser 380 contains an On Off Button 382 which the user can depress if the Drug Dispenser 380 does not automatically come on when the Drug Specific App 10 handshakes with the Drug Dispenser 380 .
  • On Off Button 382 When a handshake is effectuated or the On Off Button 382 are pushed, a blue led light comes on 384 .
  • the light 384 turns to green if the unit is ready to dispense, yellow 384 if it is awaiting authority to dispense, and red 384 if the unit is locked and will not dispense.
  • the display on 386 resides on the center of the face, Front View, of the Drug Dispenser 380 .
  • a number of components fit on the Top Clamshell Interior 388 include: (i) the On Off Button 382 switch 390 , (ii) the LED status light 384 LED and electronics 394 ; (iii) the battery, power management, Wi-Fi, Bluetooth, GPS and antenna systems 392 ; (iv) the LED Screen 386 electronics and management system 396 ; and (v) the drug dispensing actuator arm and dispensing lock 398 .
  • the Bottom Clamshell Interior 400 houses the: (vi) single click Dispensing Button 402 ; (vii) the Logic, Controls, Processor and Memory Board and its various components 404 ; (viii) Temperature and Humidity sensors 406 ; (iv) the Attempting Tampering Sensors 412 ; (x) the Cassette Rotation Motor and Controller (works like a CD-Rom rotator) 410 ; (xi) the Drug Cassette Reader 408 ; (xii) the Clamshell Lock microactuator controller 414 , and (xiii) the Dispensing Door Controller 416 .
  • the embodiment of the invention can be utilized, for among other uses, 1) to improve the drug's safety profile by ensuring proper, personalized drug utilization (e.g., Dispensing), 2) as a diagnostic aid/tool, 3) to preclude drug related adverse events, 4) to decrease the chance of addiction, 5) to preclude overdosing, 6) to manage drug dependence withdrawal, 7) to manage oral patient controlled analgesia, 7) to preclude drug divergence, 8) to guard the medication against accidental ingestion by a child, and 9) to capture the information required and control drug dispensing during clinical trials.
  • personalized drug utilization e.g., Dispensing
  • 3) to preclude drug related adverse events
  • 4) to decrease the chance of addiction 5) to preclude overdosing
  • 6) to manage drug dependence withdrawal 7) to manage oral patient controlled analgesia, 7) to preclude drug divergence, 8) to guard the medication against accidental ingestion by a child, and 9) to capture the information required and control drug dispensing during clinical trials.
  • Ensuring the proper utilization of antihypertensive medications serves as an example of how the embodiment can be used to ensure proper drug utilization. As patients get older, they have a tendency to gain weight and to develop comorbidities. These factors can interfere with how the medication is metabolized and alter the need or effectiveness of the drug over time. As a result, certain patients may become dizzy or faint as a result of a hypotensive event. If the patient is prescribed an antihypertensive, it is beneficial to prevent a potential hypotensive event, especially as it may lead to an untoward accident.
  • the patient would be prescribed an antihypertensive dispensed using the Drug Specific App 10 controlled Drug Dispenser 30 .
  • the Drug Specific Dispensing Algorithm 15 would automatically check to ensure the drug has not expired, and if it has not, then to see if it has been stored correctly, and if the Drug has been stored correctly, then, for example, it would handshake with designated devices to digitally capture blood pressure and heart rate information. Thereafter, it asks the Patient 50 at least one Patient Self-Assessment question.
  • Examples include but are not limited to: (i) have you gotten dizzy since the last time you took your antihypertensive medication, (ii) do you have blurry vision, (iii) have you felt like fainting since you took your last antihypertensive, etc. If the patient answered yes to any of the Patient Self-Assessment questions, the Drug Specific Dispensing Algorithm 15 would check the trending of the Patient's 50 blood pressure and heart rate information since the last dose.
  • the Drug Specific Dispensing Algorithm 15 would lock the Drug Dispenser 30 and inform the Patient 50 that he/she should call the Integrated Support Center 40 or talk with their Prescriber 60 or a physician prior to being able to dispense the next dose, even if the dose is within prescribing parameters.
  • the Disease Management representative at the Integrated Support Center 40 can decide within their operating constraints whether or not to unlock the Drug Dispenser 30 and allow the Patient 50 to dispense and take the prescribe antihypertensive.
  • the representative would send an email, text, and/or call the Prescriber 60 to advise him/her that an adjustment has to be made to the Patient's 50 hypertension treatment.
  • the Drug Dispenser 30 can then be unlocked and allowed to dispense the medication if those are the Prescriber's 60 instructions or the prescription can be changed based upon the Prescriber's 60 instructions.
  • an accident and/or costlier intervention can be averted, the drug efficacy for the specific Patient 50 is assured, the patient's quality of care is personalized and improved, and the patient's quality of life is enhanced.
  • the embodiment of the Invention can also be utilized to assist in diagnosis.
  • OTC over the counter
  • analgesics such as aspirin.
  • patients will generally begin by self-medicating with over the counter (OTC) analgesics such as aspirin.
  • OTC over the counter
  • patients increase the number of tablets taken (i.e., the dosage), as well as the frequency of self-medication. At a certain point, they go to their doctor seeking adequate relief.
  • Headaches represents an example. It is important to figure out what type of headache is causing the pain. If the doctor knows the type of headache, he/she can treat it correctly. However, as was highlighted by a 2004 study, 80% of people who had a recent history of self-described or doctor-diagnosed sinus headache, but no signs of sinus infection, actually met the criteria for migraine. The following discusses the different types of headaches:
  • Diagnosis requires a headache evaluation that includes: (i) headache history, (ii) description of the headaches, (iii) headache symptoms, (iv) characteristics, (v) a list of things that cause the headache, (vi) aggravate the headache, and (vii) things the patient has done to relieve a headache. The patient is also requested to keep a headache diary.
  • the proper treatment will depend on several factors, including the type and frequency of the headache and its cause. There are many migraine and headache medications and other treatments are available. The appropriate treatment often depends on the type of headache.
  • Headache pain may need to be managed with medications.
  • Headache drugs used to treat headache pain can be grouped into three different categories: symptomatic relief (drugs used to treat the headache pain or accompanying symptoms of migraines like nausea), abortive therapy (drugs used to stop a migraine headache), and preventive therapy (drugs used to prevent a migraine).
  • Botox injections represents another migraine and headache treatment.
  • the embodiment of the Invention enables the aggregation of Patient 50 specific dispensing information and Patient Self-Assessment information specifically developed to assist in the diagnosis and management of headaches.
  • Cystic fibrosis serves as an example of how the system can be utilized to manage complex drug therapy. There is no cure for CF, but treatment can ease symptoms and reduce complications, physician office visits and hospitalizations. Close monitoring and early, aggressive intervention is recommended.
  • Managing CF is complex, so treatment is best if managed by a center that specializes in cystic fibrosis.
  • the goals of treatment include: (i) preventing and controlling lung infections, (ii) loosening and removing mucus from the lungs, (iii) preventing and treating intestinal blockage, (iv) providing adequate nutrition, and (v) medications.
  • the patient must take multiple drugs, the schedule and combination which must be personalized for each patient.
  • the medicines include those to help treat or prevent lung infections, reduce swelling and open up the airways, and thin mucus. If the patient has mutations in a gene called G551D, which occurs in about 5 percent of people who have CF, the doctor may prescribe the oral medicine ivacaftor (approved for people with CF who are 6 years of age and older). Adherence and persistence with each drug regimen is critical to avoid costly complications.
  • the options include:
  • the embodiment of the Invention enables the complex management of the CF Patient 50 via the utilization of the Multi-Drug Dispenser 280 .
  • the Consolidated Therapy App 270 consolidates from two to as many Drug Specific Apps 10 as are resident on the Interface Device 20 into a single user interface for all drugs—eliminating duplicate logins, entries, and record keeping. It in turn digitally handshakes with the Multi-Drug Dispenser 280 and uses the individual Drug Specific Dispensing Algorithms 15 to control dispensing of each individual medication. Furthermore, it coordinates the dispensing schedules to have as few dispensing times, within the respective prescriptions, as possible. Multi-Drug Dispenser 280 eliminates concerns about which drugs have to be taken when.
  • Dispensing System simplifies CF drug management, encourages prescription compliance and persistence, avoids complications, and thereby reduces the total cost of treating a CF patient by decreasing the number of physician interventions and hospitalizations.
  • Opioid medications examples include: codeine, fentanyl and analogs, hydrocodone, hydromorphone, methadone, oxycodone, Oxymorphone, etc.
  • Opioid medications are effective in controlling pain.
  • physicians are reluctant to prescribe them due to their overdose, abuse, addiction and divergence potential and related REMS programs. Some patients are also reluctant to take them due to their addiction potential.
  • the embodiment provides control and real time monitoring and thereby address each of these shortcomings.
  • Overdosing is addressed by the inability of the patient to dispense a dose more frequently than allowed by the prescription. This is handled by the Drug Specific Dispensing Algorithm 15 which controls dispensing by the Drug Dispenser 30 .
  • the Drug Specific Drug Cassette 240 can only be docked with the Drug Dispenser 244 by an authorized medical professional. Any attempt by an unauthorized person to open the Drug Dispenser 244 triggers a signal to the Drug Specific App 10 which automatically locks the Drug Dispenser 244 and alerts the Integrated Support Center 40 . The Integrated Support Center 40 then calls the Patient 50 to ascertain why they are trying to open the Drug Dispenser 30 .
  • the Integrated Support Center 40 works with the Patient 50 to address any dispensing related issues and unlocks the Drug Dispenser 30 or, if attempted abuse is suspected, contacts the Prescriber 60 to alert them of the conversation with the Patient 50 and asks the Prescriber 60 whether or not the Drug Dispenser 30 should remain locked or if it should be unlocked. If authorized, the Integrated Support Center 40 updates the Electronic Medical Record 70 related to the calls to the Patient 50 and the Prescriber 60 .
  • the potential for addiction is mitigated by: (i) the patient's inability to dose more frequently than the prescribed medication schedule, (ii) by tracking attempted earlier than prescribed dosing events, (iii) by capturing any attempts to open the Drug Dispenser 30 , and (iv) through the use of patient self-assessment 100 , 102 , 104 and/or digitally captured relevant information, trended over time, to ascertain the effectiveness of the drug on the specific patient.
  • the centralized drug specific patient and population focused analytics programs 290 are designed to take a myriad of patient specific actions and inputs into account in order to identify potential movement of the Patient 50 toward addiction.
  • the analytics software 290 is programmed to alert the Integrated Support Center 40 so they may alert the Prescriber 60 and update the patient's Electronic Medical Record 70 .
  • the system is designed to comply with the respective REMS program and to virtually eliminate required data capture and automate patient specific tracking and dispensing report preparation.
  • the Integrated Support Center 40 will also support the Prescriber 60 by preparing the required REMS reports encompassing all his/her patients.
  • the system also allows for the redefinition of Prescription Drug Monitoring Programs by closing the loop between pharmacies and healthcare providers and the patient by controlling and tracking use on an individual patient basis.
  • Attributes of the system enable oral patient controlled analgesia. Studies have shown that patients that have the ability to self-medicate as warranted, e.g., PRN with set prescription parameters, tend to use less medication, further mitigating potential side effects.
  • the system may also be utilized to predict, for example, opioid related constipation and to alert the patient to take a laxative at the appropriate time. If the system's multi-drug dispenser is utilized, the program can dispense the laxative as well as the opioid and/or other medication as prescribed.
  • Addiction is a global crisis with an estimated 2.4 million opioid-dependent people in United States, 1.3 million in Europe and twenty million in the rest of the world. Opioid overdose is the second leading cause of accidental death in the US. Overdoses claimed 16,000 lives in the United States alone in 2012.
  • Addiction can either be treated with buprenorphine and/or naloxone (examples of brand names include Butrans, Suboxone, Zubsolv).
  • withdrawal must be managed through the gradual decrease of doses of the dependent drug (e.g., barbiturates, benzodiazepines, methamphetamines, narcotics, opioids, methadone, etc.).
  • Overdosing is addressed by the inability of the patient to dispense a dose more frequently than allowed by the prescription. This is handled by the Drug Specific Dispensing Algorithm 15 which controls dispensing by the Drug Dispenser 30 . The controls are in place even for the Drug Specific App 10 and Drug Dispenser 30 enabled oral PRN dosing regimen.
  • the Drug Specific Drug Cassette 240 can only be docked with the Drug Dispenser 244 by an authorized medical professional. Any attempt by an unauthorized person to open the Drug Dispenser 244 triggers a signal to the Drug Specific App 10 which automatically locks the Drug Dispenser 244 and alerts the Integrated Support Center 40 . The Integrated Support Center 40 then calls the Patient 50 to ascertain why they are trying to open the Drug Dispenser 30 .
  • the Integrated Support Center 40 works with the Patient 50 to address any dispensing related issues and unlocks the Drug Dispenser 30 or, if attempted abuse is suspected, contacts the Prescriber 60 to alert them of the conversation with the Patient 50 and asks the Prescriber 60 whether or not the Drug Dispenser 30 should remain locked or if it should be unlocked. If authorized, the Integrated Support Center 40 updates the Electronic Medical Record 70 related to the calls to the Patient 50 and the Prescriber 60 .
  • the potential for addiction is mitigated by: (i) the patient's inability to dose more frequently than the prescribed medication schedule, (ii) by tracking attempted earlier than prescribed dosing events, (iii) by capturing any attempts to open the Drug Dispenser 30 , and (iv) through the use of patient self-assessment 100 , 102 , 104 and/or digitally captured relevant information, trended over time, to ascertain the effectiveness of the drug on the specific patient.
  • the centralized drug specific patient and population focused analytics programs 290 are designed to take a myriad of patient specific actions and inputs into account in order to identify potential movement of the Patient 50 toward addiction.
  • the analytics software 290 is programmed to alert the Integrated Support Center 40 so they may alert the Prescriber 60 and update the patient's Electronic Medical Record 70 .
  • the system is designed to comply with the respective REMS program and to virtually eliminate required data capture and automate patient specific tracking and dispensing report preparation.
  • the Integrated Support Center 40 will also support the Prescriber 60 by preparing the required REMS reports encompassing all his/her patients.
  • the system is designed to capture, store, analyze, and act upon drug specific patient reported self-assessment (AKA self-reported outcomes, patient-reported outcomes, PROs, etc.) and digitally captured physiological, psychological, lifestyle, other drugs currently being taken, and environmental information along with the drug's prescription and drug dispensing history in order for the Drug Specific App 10 to decide if the drug should or should not be dispensed. Dispensing can be precluded by the Drug Specific App 15 if the required dispensing criteria are not met, even if without the self assessment and digitally captured data, the prescription would normally allow dispensing.
  • PROs patient-reported outcomes
  • Interest in developing and applying patient-reported outcomes (PROs) across the drug development and postmarket spectrum is growing—among sponsors, clinicians, payers, regulators and patients.
  • a growing number of clinical trials now are going beyond conventional randomized control measurements to collect self-reported outcomes from patients—focusing on improving patients' involvement by including their perspectives throughout the drug development process.
  • An analysis of sponsor-funded interventional studies listed on CenterWatch's Clinical Trials Listing Service found between 2005 and 2007, only 6.1% of total study procedures involved some type of subjective outcome assessment. That grew to 11.8% in the 2008 to 2010 timeframe and, most recently, between 2011 and 2013, increased to 16.3% of total study procedures.
  • PROs can capture a range of information, from symptom changes and level of functioning, to health-related qualify of life and treatment satisfaction and adherence.
  • PRO use often is inconsistent and underutilized in understanding how patients feel in relation to their diseases, such as cancer, cardiovascular disease, diabetes, etc.
  • regulatory agencies do not require sponsors to consider PROs in clinical trials and, until recently, did not do much to encourage their use.
  • signs point to that sentiment is changing.
  • Janet Woodcock, M.D., director of the FDA's Center for Drug Evaluation & Research (CDER) stated: “We understand that people with chronic diseases are experts in that disease, as far as the symptoms and the impact on quality of life, and what might be acceptable tradeoffs on risk and uncertainty.
  • PROs generally are used as primary endpoints in clinical trials in indications such as migraines and irritable bowel syndrome, in which specific symptoms play a major role in treatment. PROs also are important in the final product labeling manufacturers are allowed to use to promote their products, and to clinicians seeking information to support their prescribing choices. Now, trials for psychiatric and age-related illnesses, among others, are including PROs as part of the protocol design.
  • PROs Pain studies initially used PROs as a primary outcome in a clinical trial because attempts to obtain an objective measure of pain through a dolorimeter, a spring-loaded instrument with a gauge for measuring sensitivity to, or levels of, pain, or through a galvanic skin response lacked validity compared to simple pain scales.
  • Other disease examples where PROs are preferable include neurology, depression, anxiety, and irritable bowel syndrome (IBS) which may utilize co-primary and/or key secondary PROs.
  • IBS irritable bowel syndrome
  • RWE real world evidence
  • RWE is becoming essential for sound medical coverage, payment and reimbursement decisions, according to the International Society for Pharmaeconomics Outcomes Research Real-World Data Task Force.
  • RWE can be used with randomized clinical trials to design more efficient trials and understand a drug's benefit-risk profile, as well as to gain understanding of the market for launch planning, according to the task force.
  • RWE shows how a drug is accepted from patients who have experience using it. It reveals how a drug is utilized in different geographies and can be used to help frame policy or regulatory decisions. It is a highly credible source of information.
  • the embodiment provides:” (i) the requisite data capture, (ii) patient involvement, (iii) dispensing control, (iv) avoidance of certain drug related side effects, (v) real time reminders for the patient to take the medication, (vi) intervention alerts if the patient fails to take their medication within a predefined time interval, (vii) dispensing tracking (date and time), (viii) real time monitoring, and (ix) reporting. It addresses the shortcomings of current systems to capture and compile real time, patient and drug specific data to facilitate ongoing clinical trial data aggregation, analysis, and reporting while minimizing the number of calls to the clinical trial physician.
  • the patient would be prescribed the medication to be dispensed per a defined prescription using the Drug Specific App 10 controlled Drug Dispenser 30 .
  • the Drug Specific Dispensing Algorithm 15 automatically handshakes with the Drug Dispenser 30 , handshakes with defined digital devices (e.g., blood pressure, heart rate, etc.) FIG. 5 and downloads the latest data to the Interface Device's 20 Drug Specific App 10 data base, checks to ensure the drug has not expired, and if it has not, then to see if it has been stored correctly. If the Drug has been stored correctly, then, for example, it automatically moves to the next screen and asks the Patient 50 to answer the specific questions.
  • defined digital devices e.g., blood pressure, heart rate, etc.
  • the Patient 50 would answer the PRO and data capture screens 194 to 214 required by the FDA and EMA to get approval for a 5HT3 drug to treat IBS-D.
  • the ability to capture the requisite PRO primary and secondary end point data and the related compliance and persistence data are illustrated in FIG. 8 . These screens can be configured to capture and aggregate drug specific information.
  • the Drug Specific Dispensing Algorithm 15 then utilizes its decision tree FIG. 6 to check the prescription instructions and when the drug was last dispensed to ascertain if the drug can be dispensed. It then either generates a screen stating that the dose will not be authorized for a specific period of time 222 or proceeds to ascertain if the designated digital and self-assessment reported values allow the medication to be dispensed. If yes, then the screen shows a green dispense 216 .
  • the Drug Specific Dispensing Algorithm 15 indicates that the patient should not receive the medication, even if it is within the prescription guidelines, then it will either generate, for example, a screen stating that the dose is not warranted at the specific time and provide the Patient 50 the ability to click on dial to call the Integrated Support Center 40 or if a problem is ascertained, it will either show a specifically designed screen or a screen that the Integrated Support Center should be called 224 .
  • the type and sequence of screens is dictated by the drug's clinical trial data capture requirements.
  • the algorithm can contain routines that only ask for specific information if certain predefined criteria are met.
  • the embodiment allows for better prescription compliance, an improved drug safety profile, increased prescription persistence, uniform data capture, facilitates data analysis, decreases required interventions by the clinical trial physician(s), decreases the cost of the trial, and provides real time data capture and analysis.
  • the Drug Specific App 10 is capable of being programmed to control PRN dosing in various configurations and schedules. This allows for real time data capture which is useful in in diagnosis, patient management, and dispensing control.
  • IBS-D diarrhea predominant irritable bowel syndrome
  • Lostronex® (alosetron), a 5HT 3 , approved only in the United States which requires a complex REMS program, serves an example of how the Embodiment can transform drugs that failed to get approval with similar profiles into approvable agents.
  • Lostronex® should be started at a dosage of 0.5 mg twice a day. Patients who become constipated at this dosage should stop taking Lostronex® until the constipation resolves. They may be restarted at 0.5 mg once a day. If constipation recurs at the lower dose, Lostronex® should be discontinued immediately.
  • Cilansetron a more potent 5HT3 antagonist for the treatment of IBS-D failed to get FDA and European regulatory approval because of the concerns related to potential constipation that could potentially lead to ischemic colitis.
  • the utilization of the system designed to identify and block dispensing FIG. 4 if potential constipation is suspected would address this concern. If we use the Lotronex® example, the system could also change the dosing to allow PRN dosing using, for example, 0.5 mg for up to four times per day. This would control the maximum dosing to 2 mg per day. The system would ensure compliance with the prescription and would protect against potential constipation.

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Abstract

The present invention describes a novel system, drug delivery device, mobile App, drug specific drug dispensing algorithm, and method to improve medication safety and effectiveness via the utilization of drug specific algorithms to control drug dispensing, avoid drug mediated adverse events, ensure prescription persistence and promote prescription compliance on a cost-effective real-time basis.

Description

    CROSS REFERENCE TO RELATED APPLICATIONS
  • This application is a continuation of U.S. patent application Ser. No. 15/751,371 filed on Feb. 8, 2018, which is a national stage entry of International Application No. PCT/US2016/046491, filed on Aug. 11, 2016, which claims benefit of U.S. Provisional Patent Application No. 62/203,638 filed on Aug. 11, 2015 and U.S. Provisional Patent Application No. 62/252,966 filed on Nov. 9, 2015; which are incorporated herein by reference in their entirety to the full extent permitted by law.
  • FIELD OF THE INVENTION
  • The present disclosure relates to a novel system to improve medication safety and effectiveness via the utilization of drug specific algorithms to control drug dispensing, avoid drug mediated adverse events, ensure prescription compliance and promote prescription persistence on a cost-effective real-time basis.
  • BACKGROUND OF THE INVENTION
  • Avoiding unnecessary medical complications or death by ensuring a drug is efficacious for the patient and that the patient is compliant and persistent with their prescription(s) represents a major unmet need and a trillion-dollar global market opportunity—this is larger than the global pharmaceutical industry. As an example, according to Express Scripts, the largest pharmacy benefit manager in the United States, only 25 to 30 percent of medications are taken per the prescriber's instructions (adherence) . . . and of those taken, only 15 to 20 percent are refilled per the prescriber's instructions (persistence). This lack of adherence and persistence is estimated to result in excess of $300 billion being wasted annually for the treatment of unnecessary medical complications in the United States.
  • Drug-related hospitalizations account for 2.4 to 6.5 percent of all medical admissions in the general population. A meta-analysis found a fourfold increase in the rate of hospitalization related to adverse drug events (ADE) in older adults compared with younger adults (16.6 versus 4.1 percent). A number of factors in older individuals contribute to their increased risk for developing a drug-related problem. These include frailty, coexisting medical problems, memory issues, polypharmacy, and the use of non-prescribed medications. Estimates indicate that 88 percent of the ADE hospitalizations among older adults were preventable, compared with 24 percent among young persons
  • Optimizing drug therapy is an essential part of medical care. The process of prescribing a medication is complex and includes (i) deciding that a drug is indicated, (ii) choosing the best drug, (iii) determining a dose and schedule appropriate for the patient's physiologic status, (iv) monitoring for effectiveness and toxicity, (v) educating the patient about expected side effects, and (vi) indications for seeking consultation.
  • Avoidable adverse drug events are the serious consequence of (i) inappropriate drug prescribing, (ii) changes in the patient's reaction to the drug over time due to lifestyle, other medications, other medical conditions, worsening medical condition, or changes in the patients overall well-being, etc., or (iii) addition of new prescription or OTC medications, vitamins, dietary supplements, herbal medicines (e.g., ginseng, ginkgo biloba extract, glucosamine, St. John's wort, echinacea, garlic, saw palmetto, kava, and valerian root), and/or recreational drugs, etc. Often, clinicians do not question patients about use of herbal medicines and patients do not routinely volunteer this information. Furthermore, most patients do not inform their clinician that they were using unconventional and/or recreational medications. A study of the use of 22 supplements in a survey of 369 patients aged 60 to 99 years found potential interactions between supplements and medications for ten of the 22 supplements surveyed. As a result, any new symptom should first be considered to be drug-related until proven otherwise.
  • Prescribing for older patients, who consume the most medications per capita, presents unique challenges. Premarketing drug trials often exclude geriatric patients and approved doses may not be appropriate for older adults. Many medications need to be used with special caution because of age-related changes in pharmacokinetics (i.e., absorption, distribution, metabolism, and excretion) and pharmacodynamics (the physiologic effects of the drug).
  • Larger drug storage reservoirs and decreased clearance prolong drug half-lives and lead to increased plasma drug concentrations in older people. Particular care must be taken in determining drug dosages. The proportional increase in body fat relative to skeletal muscle that generally accompanies aging may result in the increased volume of drug distribution. Decreased drug clearance may also result from the natural decline in renal function with age, even in the absence of renal disease.
  • The same dose could lead to higher plasma concentrations in an older, compared to younger, patient. For example, the volume of distribution for diazepam is increased, and the clearance rate for lithium is reduced, in older adults. From the pharmacodynamic perspective, increasing age may result in an increased sensitivity to the effects of certain drugs, e.g., benzodiazepines and opioids.
  • The use of greater numbers of drug therapies has been independently associated with an increased risk for an adverse drug event, irrespective of age, and increased risk of hospital admission. Polypharmacy is of particular concern in older people who, compared to younger individuals, tend to have more disease conditions for which therapies are prescribed. Approximately half of the patients taking drugs take two medications and 20 percent five or more. As an example, one study found that among ambulatory older adults with cancer, 84 percent were receiving five or more and 43 percent were receiving 10 or more medications.
  • The risk of an adverse event due to drug-drug interactions is substantially increased when multiple drugs are taken. For example, the risk of bleeding with warfarin therapy is increased with coadministration of selective and non-selective NSAIDs, SSRIs, omeprazole, lipid-lowering agents, amiodarone, and fluorouracil. A study found hospitalizations for hypoglycemia was six times more likely in patients who had received co-trimoxazole. Digoxin toxicity was 12 times more likely for patients who had been started on clarithromycin. Hyperkalemia was 20 times more likely for patients who were treated with a potassium sparing diuretic.
  • Periodic evaluation of a patient's drug regimen is an essential component of medical care. However, a survey of Medicare beneficiaries found that more than 30 percent of patients reported they had not talked with their doctor about their different medications in the previous 12 months. Furthermore, when these reviews are done, they often overlook OTC, supplements, herbal medicines and recreational drugs that are being taken by the patient.
  • Multiple factors contribute to the appropriateness and overall quality of drug prescribing. These include avoidance of inappropriate medications, appropriate use of indicated medications, monitoring for side effects and drug levels, avoidance of drug-drug interactions, and involvement of the patient and integration of patient values. Current measures of the quality of prescribing generally focus on one or some of these factors, but rarely on all.
  • BRIEF SUMMARY OF THE INVENTION
  • The present invention describes novel methods and drug dispensing devices, drug specific Apps, drug specific dispensing algorithms, and an integrated support center to ensure any oral medication taken by a patient is efficacious; is only dispensed as prescribed by the healthcare professional (e.g., physician, physician's assistant, nurse practitioner, pharmacist, etc.); is not dispensed if (i) the patient is trying to take the medication sooner than the prescribed interval, (ii) the algorithm deduces that taking the drug may result in an adverse event, even if it could be dispensed within the prescription's guidelines (iii) the drug is past its expiration date, (iv) the drug was not stored properly, e.g., within the right temperature and/or humidity guidelines, and/or (v) the drug batch has been recalled, etc.; and encourages the patient to continue taking the medication as prescribed. In this way, by increasing the drug's efficacy/safety profile, the dispensing system saves the healthcare system money by decreasing the number of interventions, physician's office visits, and hospitalizations—reducing the total cost of care.
  • The drug specific dispensing algorithm uses encrypted communications to control the drug dispensing device and to communicate with the patient and the support center. The algorithm uses the prescription information, dispensing device information, drug cassette information, patient self-assessment and/or digitally captured physiological, psychological, lifestyle, medications currently being taken, and/or environmental data in a novel drug specific diagnostic algorithm to decide if the drug dispenser should dispense the drug or keep the tamper resistant dispensing unit locked.
  • The novel drug specific App, which can be operated from a standalone drug dispensing device, interface device (smart phone, tablet and/or computer, or standalone drug dispensing device, etc. with Internet communication capabilities), reads and aggregates; (i) the drug information from the drug cassette, (ii) the devices serial number, operating, environmental and dispensing information from the dispensing device, (iii) patient self-assessment data from input screens on the standalone dispenser, smart phone, tablet, and/or computer, etc., and (iv) digital data generated by wearable devices, consumed, implanted, or injected diagnostic devices, monitoring devices, machines, instruments, gadgets, contraptions, apparatuses, utensils, implements, tools, mechanisms, and informalgizmos, etc.
  • The drug dispensing device is designed to automatically recognize the drug based upon the drug specific disposable drug cassette docked into the device. The cassette is marked to allow the drug dispenser to ascertain the name of the drug (brand and/or generic), the drug's NDC number, the drug batch number, and drug's expiration date, etc.
  • The drug dispensing device is designed to be water proof, tamper resistant, withstand being dropped and/or banged, operate and withstand hot and cold temperatures within defined temperature ranges, to be reusable and rechargeable, to have the drug cassette only docked or removed by a healthcare professional, to remain locked from dispensing unless the dispensing device receives an encrypted signal from the authorized smart App, and to dispense the drug with one click. The device, when interfaced with the drug specific App, transmits its serial number via a secure handshake with the App, reads and transmits the drug information on the drug cassette, transmits the current and historic temperatures since the last dispense, and the date and time the drug is dispensed. The drug dispensing device can be configured to dispense one or more drugs and to be controlled by one or more dispensing Apps, one App for each drug.
  • The multi-drug dispensing units utilize multiple drug cassettes (one each per drug) which are controlled by a consolidation App that combines the individual drug Apps into a single user interface to eliminate duplication of inputs and to facilitate one click drug dispensing for one or more medications. The handshake between Apps is controlled by the biometric security system.
  • The single drug App, as well as the multi-drug App, require biometric sign on by the patient and utilize a drug specific decision tree algorithm to make dispensing decisions. An encrypted sign on alternative may also be provided. No messages or further communication with the patient are required if drug dispensing is within prescribing guidelines and no potential adverse events are detected by the algorithm. However, if the algorithm decides to keep the dispensing unit locked and not to dispense, even if within prescribing guidelines, then a number of alternative messages are shown on the interface device (standalone dispensing unit, smart phone, tablet, and/or computer, etc. with Internet communications capabilities). These range from telling the patient that the next dose is not authorized by the prescription for a specified period of time to a message indicating that a dose, even within the prescription dosing schedule parameters, should not be taken without first talking with the integrated support center (which serves as a disease management center for patients) or the prescribing healthcare professional. The App facilitates calling the support center using a single click on the alert window.
  • The App uses the biometric sign on and encrypted communications with the support center to let them know if, for example, (i) the patient may be heading for an undesired event, (ii) that the prescription should be changed, (iii) the drug may have to be changed based upon efficacy concerns, (iv) the patient tries early dispensing too many times (depends on the drug type, e.g., opioids), (iv) appears to be following an abuse pattern, etc., (v) is not following prescribing guidelines, and (vi) is failing to take the medication, etc.
  • The App allows the patient to ask certain questions regarding when they took their last medication (or medications for multidrug dispensers), how much medication is left, when their next dose is due, the medications expiration date, and the drugs package insert information, etc. It further provides access to personalized analytical charts, some which may be downloaded from the integrated support center's servers or created by the App from the limited information stored by the App, to show how the patient's symptoms are affected when the patient takes a drug dose. This is designed to aid in patient prescription persistence and assist in reinforcing the importance of prescription compliance.
  • The integrated support center IT system stores authorized log on information, all App history data and enables the continual update of the App history on all the patient's devices where the App has been downloaded. The centralized servers are also designed to: (i) update individual App software as required, (ii) exchange information with authorized electronic medical records, (iii) to, on a real time basis, update the call center's disease management patient specific counselor screens, (iv) conduct metadata analysis on both the patient's individual data as well as analysis that may include information from the patient's electronic medical record, (v) carry out comparative patient analysis against metadata across a patient population with similar characteristics, etc. The analytical output is designed to assist the call center's disease management group in its counseling of the individual patient as well as any reporting and contacts with the patient's prescribing medical professional.
  • The call center IT systems are designed to allow the call center, via the patient's drug specific App, (i) to change a patient's prescription based on an authorized prescriber's instructions, (ii) to lock and unlock the dispensing ability on the individual drug dispensing unit based upon a discussion with the patient and/or his care giver, and (iii) to lock all appropriate dispensing devices that contain a recalled drug and to instruct the patient via email and/or voice messages to go to their pharmacy to get the drug replaced or to follow the recalling manufacturer's instructions.
  • The call center's disease management team uses metadata analysis as well as drug registry information, as requested by the prescribing medical profession, to assist them in developing the best course of therapy based on specific queries of the integrated support center's databases and any authorized related electronic medical records.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • Advantages of embodiments of the present invention will be apparent from the following detailed description of the exemplary embodiments thereof, which description should be considered in conjunction with the accompanying drawings in which:
  • FIG. 1 is an exemplary embodiment of a closed loop system controlled by a Drug Specific Dispensing Algorithm.
  • FIG. 2 is an exemplary embodiment showing a Drug Specific App which controls the Drug Dispensing Unit.
  • FIG. 3 is an exemplary embodiment of a Biometric Authentication screen.
  • FIG. 4 is an exemplary embodiment of Patient Self-Assessment Screens.
  • FIG. 5 is an exemplary embodiment of digitally available patient related diagnostic and physiological information.
  • FIG. 6 is an exemplary embodiment of a flow chart/decision tree used by the Drug Dispensing Algorithm.
  • FIGS. 7A and 7B are an exemplary embodiment of a flow chart of a standard prescription log in, Patient Self-Assessment and drug dispensing control.
  • FIGS. 8A-8D are an exemplary embodiment of the flow chart of the respective screens utilized to capture clinical trial data and to control the drug dispensing.
  • FIG. 9 is an exemplary embodiment of a Drug Dispenser.
  • FIG. 10 is an exemplary embodiment of a Drug Cassette.
  • FIG. 11 is an exemplary embodiment of Patient Self-Assessment Reporting Screens.
  • FIG. 12 is an exemplary embodiment of the Consolidated Therapy App and various Multi-Drug Dispensing devices.
  • FIG. 13 is an exemplary embodiment of the Centralized IT System.
  • FIG. 14 is an exemplary embodiment of an Integrated Support Center.
  • FIG. 15 is an exemplary embodiment of the design for a single drug Drug Dispenser.
  • FIG. 16 is an exemplary embodiment of how the Drug Dispenser's clam shell design is assembled for secure closing and opening.
  • FIG. 17 is an exemplary embodiment of the electronic schematic for the Drug Dispenser.
  • FIG. 18 is an exemplary embodiment of the placement of electronics and mechanical components on the outside and within the Drug Dispenser.
  • DETAILED DESCRIPTION OF THE INVENTION I. Terms and Acronyms
  • Terms used in this document, AKA denotes terms used interchangeably:
  • Adverse Event (AKA: AE, Adverse Event, Adverse Experience, Adverse Drug Reaction, ADR, or Unexpected Adverse Drug Reaction) refers to (i) a medical occurrence temporally associated with the use of a medicinal product, but not necessarily causally related, (ii) any response to a drug which is noxious and unintended, and which occurs at doses normally used in man for the prophylaxis, diagnosis, or therapy of disease, or for the modifications of physiological function, (iii) an unexpected reaction not consistent with applicable product information or characteristics of the drug, and (iv) the unintended effect occurring at normal dose related to the pharmacological properties of a medication, etc.
  • Biometric Authentication (AKA biometric identification and biometric authentication.) The definition encompasses but is not limited to biometric technologies that digitally capture fingerprint, palm and full-hand scanners, voice, facial recognition systems, iris scanning technology, document readers, biometric software, and related services capable of wireless, mobile or stationary use to limit access to the Patient. In this document the term also incorporates any system, while not biometric, that allows access via the use of a Login Name in combination with a Password and/or any additional security information.
  • Consolidation App (AKA multiunit dispenser App) is an App designed to recognize other Drug Specific Apps resident on an Interface Device and then to consolidate the requisite Patient Self-Assessment screens into a single interface for the control and dispensing of multiple drugs.
  • Digitally Captured refers to Patient data captured by diagnostic or monitoring devices and stored in a machine readable format.
  • Dispensing Device refers to the Drug Dispensing Unit with a Docked Drug Cassette whose dispensing is controlled by a Drug Specific App.
  • Dispensing System is comprised of the Dispensing Device and the Integrated Support Center.
  • Docked refers to the Drug Cassette residing in the Drug Dispensing Unit.
  • Drug (AKA pharmaceutical, medication, medicament, OTC drug, supplement, or herbal remedy, etc.)
  • Drug Cassette is the disposable unit that contains a Drug to be dispensed over a defined period of time and/or days per the prescription instructions.
  • Drug Dispensing Unit is the device where the Drug Cassette is Docked and whose dispensing mechanism (lock, unlock, and dispensing) are controlled by a Drug Specific App.
  • Drug Specific App refers to an app that requires Biometric Authentication prior to a Patient being able to respond to Patient Self-Assessment screens which are used by the App's Drug Specific Dispensing Algorithm to decide whether or not to signal the Dispensing Device to dispense the medication or to indicate to the patient and/or Integrated Support Center why the drug will not be dispensed.
  • Drug Specific Dispensing Algorithm refers to the decision tree based algorithm specifically develop for each drug to ascertain if the drug should or should not be dispensed.
  • Electronic Medical Record (AKA EMR, Patient Medical Record, PMR, etc.)
  • Encryption (AKA Encrypted, Encrypted communications) is the most effective way to achieve data security. Access requires a secret key or password that enables decryption. Unencrypted data is called plain text; encrypted data is referred to as cipher text.
  • Expiration Date refers to the date after which a medication should not be taken.
  • Handshake (AKA Digital Handshake) refers to an exchange of signals between devices ensuring synchronization whenever a connection, as with another device, is initially established.
  • Integrated Support Center refers to a call center designed to provide patient support, disease management services and/or Dispensing Device support for patients, Prescribers, and/or payers.
  • Interface Device refers to the device (standalone drug delivery device, smart phone, tablet, computer, etc. with Internet communications capabilities) where the Drug Specific App resides.
  • Locked indicates the drug cannot be dispensed by the Dispensing Device until the Drug Specific App unlocks the Dispensing Device.
  • Metadata Analysis (AKA structural metadata and descriptive metadata) as used herein refers to the use of the organization of patient data to enable analysis of both individual and patient population data to ascertain how to best manage medication therapy on a drug by drug and patient by patient basis.
  • Patient refers to the individual that is prescribed and is taking a medication or medications. Examples include physicians, physician assistants, nurse practitioners, nurses, pharmacists, etc.
  • Patient Self-Assessment (AKA patient-reported outcome or PRO) covers a whole range of potential types of measurement self-reported by the patient. Each self-assessment scale or question measures a single underlying characteristic(s).
  • Prescriber is defined as any healthcare professional authorized by an individual country to write a prescription for a drug.
  • Recall refers to a drug recall issued by the manufacturer or a regulatory agency indicating that a particular drug batch or drug should not be taken.
  • Tamper Resistant refers to a design that makes it difficult to change, open, remove the cassette, or cause damage to the unit by anyone but authorized persons.
  • II. List of Drugs, Drug Mechanisms of Action, and Diseases that Invention in its Various Embodiments is Applicable to
  • The invention and its various embodiments can enable the personalization of drug therapy, improve each drugs safety profile, ensure the continued efficacy of a drug for each patient, improve the quality of care, improve the patients quality of life by ensuring proper prescribing and prescription compliance, by promoting prescription persistence, and thereby decreasing the number of drug related medical interventions, and disease related physician visits and hospitalizations thereby decreasing the total cost of patient care. This Invention in its various embodiments is applicable to and by reference incorporates the drugs, drug mechanisms of action, and diseases listed in Table 1-Table 8.
  • Table 1 lists oral drugs with REMS programs. The listed approved drugs are encompassed in the embodiment of the invention by reference can benefit from an improved drug safety profile. The Invention mitigates prescription risk for the drug manufacturer and prescriber as it shifts the responsibility to the patient. The listing for each drug includes by definition each drug's respective indication(s), strength, dosage form, route of administration, side effect profile, drug interactions, etc.). In addition to Table 1, the embodiment incorporates by reference the Food and Drug Administration's (FDA) Approved Risk Evaluation and Mitigation Strategies (REMS) drugs listing.
  • TABLE 1
    Oral Drugs with Required REMS Programs
    Antipsychotic
    Seroquel (Quetiapine)
    Pain Relievers
    Opioids
    Codeine
    Fentanyl and Analogs
    (Causing Overdoses)
    Hydrocodone
    Hydromorphone
    Methadone
    Oxycodone
    Oxymorphone
    Sedatives (Barbiturates)
    Amytal (amobarbital)
    Nembutal (pentobarbital)
    Seconal (secobarbital)
    Stimulants (ADHD)
    Adderall (Amphetamine)
    Methylphenidate
    Daytrana
    Concerta
    Ritalin
    Tranquilizers
    A. Benzodiazepines, Like
    Klonopin (clonazepam)
    Valium (diazepam)
    Xanax (alprazolam)
    B. Non-Benzodiazepines, Like
    Ambien (zolpidem)
    Lunesta (eszopiclone)
    Sonata (zaleplon)
    Others
    Chantix
    Revlimid
    Tracler
    Xeljans (Jak Compounds)
  • Table 2 lists the Paragraph IV Challenged Drugs that can benefit from the increased patent protection afforded by the drug/device (Invention) combination. The following approved drugs and the FDA's Paragraph IV Drug Product Applications: Generic Drug Patent Challenge Notifications list are encompassed in the embodiment of the invention by reference. The listing for each drug includes by definition each drug's respective indication(s), strength, dosage form, route of administration, side effect profile, drug interactions, etc.
  • TABLE 2
    Paragraph IV Challenged Drugs
    BRAND GENERIC NAME
    Ampyra Dalfampridine
    Daliresp Roflumilast
    Angeliq Drospirenone and Estradiol
    Nexavar Sorafenib Tosylate
    Kuvan Sapropterin Dihydrochloride
    Pradaxa Dabigatran Etexilate Mesylate
    Tradjenta Linagliptin
    Thalomid Thalidomide
    Gabitril Tiagabine Hydrochloride
    Zohydro ER Hydrocodone Bitartrate
    Viibryd Vilazodone Hydrochloride
    Abstral Fentanyl Citrate
    Letairis Ambrisentan
    Lamictal XR Lamotrigine
    Zorvolex Diclofenac
    Zytiga Abiraterone Acetate
    Ella Ulipristal Acetate
    Xartemis XR Oxycodone Hydrochloride and
    Acetaminophen
    Doryx Doxycycline Hyclate
    Noxafil Posaconazole
    Tekturna HCT Aliskiren Hemifumarate and
    Hydrochlorothiazide
    Promacta Eltrombopag Olamine
    Gilenya Fingolimod
    Afinitor Everolimus
    Gleevec Imatinib Mesylate
    Brisdelle Paroxetine
    Tikosyn Dofetilide
    Hysingla ER Hydrocodone Bitartrate
    Suboxone Buprenorphine Hydrochloride and
    Naloxone Hydrochloride
    Latuda Lurasidone Hydrochloride
    Trokendi XR Topiramate
    Contrave Naltrexone Hydrochloride and
    Bupropion Hydrochloride
    Equetro Carbamazepine
    Minastrin
    24 Fe Norethindrone Acetate and Ethinyl
    Estradiol and Ferrous Fumarate
  • Table 3: Marketed Drugs lists approved drugs which are encompassed in the embodiment of the invention by reference. Drug compounds of interest are also listed in: Goodman & Gilman's, The Pharmacological Basis of Therapeutics (12th Ed) (Goodman et al. eds) (McGraw-Hill) (2011); and 2015 Physician's Desk Reference which are also encompassed in the embodiment of the invention by reference. The listing for each drug includes by definition each drug's respective indication(s), strength, dosage form, route of administration, side effect profile, drug interactions, etc.
  • TABLE 3
    Marketed Drug
    Abilify (aripiprazole)
    Abraxane (paclitaxel protein-bound particles for injectable suspension)
    ABREVA (docosanol)
    Abstral (fentanyl sublingual tablets)
    Abthrax (raxibacumab)
    Accolate
    Accretropin (somatropin rDNA Original)
    Aciphex (rabeprazole sodium)
    Actemra (ocilizumab)
    Actemra (tocilizumab)
    Actiq
    Activella (Estradiol/Norethindrone Acetate) Tablets
    Actonel
    ACTOplus met (pioglitazone hydrochloride and metformin hydrochloride)
    ACTOS
    Acular (ketorolac tromethamine ophthalmic solution) 0.5%
    Acuvail (ketorolac tromethamine)
    Acyclovir Capsules
    Adcetris (brentuximab vedotin)
    Adcirca (tadalafil)
    Adderall (mixed salts of a single-entity amphetamine)
    Adderall XR
    Addyi (flibanserin)
    Adempas (riociguat)
    Advicor (extended-release niacin/lovastatin)
    Afinitor (everolimus)
    Afrezza (insulin human) Inhalation Powder
    Agenerase (amprenavir)
    Aggrenox
    Agrylin (anagrelide HCL)
    AK-Con-A (naphazoline ophthalmic)
    Akten (lidocaine hydrochloride)
    Akynzeo (netupitant and palonosetron)
    Alamast
    Albenza (albendazole)
    Aldara (imiquimod)
    Aldurazyme (laronidase)
    Alesse (100 mcg levonorgestrel/20 mcg ethinyl estradiol tablets)
    Alimta (pemetrexed for injection)
    Alinia (nitazoxanide)
    Allegra (fexofenadine hydrochloride)
    Allegra-D
    Alora
    Aloxi (palonosetron)
    Alphagan (brimonidine)
    AlphaNine SD Coagulation Factor IX (Human)
    Alprolix [Coagulation Factor IX (Recombinant), Fc Fusion Protein]
    Alrex
    Altabax (retapamulin)
    Altocor (lovastatin) Extended-Release Tablets
    Alvesco (ciclesonide)
    Amaryl (Glimepiride)
    Amerge
    Amevive (alefacept)
    Amitiza (lubiprostone)
    Amoxil (amoxicillin)
    Ampyra (dalfampridine)
    Amrix (cyclobenzaprine hydrochloride extended release)
    Amturnide (aliskiren + amlodipine + hydrochlorothiazide)
    Androderm (Testosterone Transdermal System)
    AndroGel testosterone gel
    AneuVysion Assay
    Anexsia
    Angiomax (bivalirudin)
    Anoro Ellipta (umeclidinium and vilanterol inhalation powder)
    Antizol Injection
    Anturol (oxybutynin) Gel
    Anzemet
    Aphthasol
    Aplenzin (bupropion hydrobromide)
    Apokyn (apomorphine hydrochloride)
    Apthasol (Amlexanox)
    Aptiom (eslicarbazepine acetate)
    Aptivus (tipranavir)
    Arava
    Arcapta (indacaterol maleate inhalation powder)
    Aredia (pamidronate disodium for injection)
    Arestin (minocycline hydrochloride)
    Argatroban Injection
    ARICEPT (donepezil hydrochloride)
    Arimidex (anastrozole)
    Arixtra
    Amuity Ellipta (fluticasone furoate inhalation powder)
    Aromasin Tablets
    Arranon (nelarabine)
    Arthrotec
    Arzerra (ofatumumab)
    Asacol (mesalamine)
    Astelin nasal spray
    Astepro (azelastine hydrochloride nasal spray)
    Atacand (candesartan cilexetil)
    Atracurium Besylate Injection
    Atridox
    Atrovent (ipratropium bromide)
    Atryn (antithrombin recombinant lyophilized powder for reconstitution)
    Aubagio (teriflunomide)
    Augmentin (amoxicillin/clavulanate)
    Auryxia (Ferric citrate)
    Avandamet (rosiglitazone maleate and metformin HCl)
    Avandia (rosiglitazone maleate)
    Avastin (bevacizumab)
    Aveed (testosterone undecanoate) injection
    Avelox I.V. (moxifloxacin hydrochloride)
    Avinza (morphine sulfate)
    Avita Gel
    Avonex (Interferon Beta 1-A)
    Avycaz (ceftazidime-avibactam)
    Axert (almotriptan malate) tablets
    Axid AR (nizatidine
    Axona (caprylidene)
    AzaSite (azithromycin)
    Azmacort (triamcinolone acetonide) Inhalation Aerosol
    Azor (amlodipine besylate; olmesartan medoxomil)
    Azulfidine EN-tabs Tablets (sulfasalazine delayed release tablets, USP)
    Bactroban Cream
    Bactroban Nasal 2% (mupirocin calcium ointment)
    Banzel (rufinamide)
    Baraclude (entecavir)
    Baycol (cerivastatin sodium)
    Bayer Extra Strength Asprin
    Beleodaq (belinostat)
    Belsomra (suvorexant)
    Belviq (lorcaserin hydrochloride)
    BeneFIX (coagulation Factor IX (recombinant))
    Benicar
    Benlysta (belimumab)
    Benzamycin (erythromycin 3%-benzoyl peroxide 5% topical gel)
    Bepreve (bepotastine besilate ophthalmic solution)
    Berinert (C1 Esterase Inhibitor (Human))
    Besivance (besifloxacin ophthalmic suspension)
    Betapace AF Tablet
    Betaxon
    Bexsero (Meningococcal Group B Vaccine)
    Bextra
    Bexxar
    Biaxin XL (clarithromycin extended-release tablets)
    BiDil (isosorbide dinitrate/hydralazine hydrochloride)
    Bio-T-Gel (testosterone gel)
    Blincyto (blinatumomab)
    Boniva (ibandronate)
    Bosulif (bosutinib)
    Botox (onabotulinumtoxinA)
    Botox Cosmetic (botulinum toxin type A)
    Bravelle (urofollitropin for injection, purified)
    Breathe Right
    Breo Ellipta (fluticasone furoate and vilanterol inhalation powder)
    Brilinta (ticagrelor)
    Brintellix (vortioxetine)
    Brisdelle (low-dose paroxetine mesylate)
    Bromfenac
    Brovana (arformoterol tartrate)
    BSS Sterile Irrigating Solution
    Bunavail (buprenorphine and naloxone)
    Busulflex
    Butrans (buprenorphine) Transdermal System
    Bydureon (exenatide extended-release for injectable suspension)
    Byetta (exenatide)
    Caduet (amlodipine/atorvastatin)
    Cafcit Injection
    Cambia (diclofenac potassium for oral solution)
    Campath
    Campostar
    Campral (acamprosate calcium)
    Camptosar
    Canasa (mesalamine)
    Cancidas
    Captopril and hydrochlorotiazide
    Carbaglu (carglumic acid)
    Carbatrol
    Cardizem (R) (Diltiazem HCl for injection) Monvial (R)
    Carrington patch
    Caverject (alprostadil)
    Cayston (aztreonam for inhalation solution)
    CEA-Scan
    Cedax (ceftibuten)
    Cefazolin and Dextrose USP
    Ceftin (cefuroxime axetil)
    Celexa
    CellCept
    Cenestin
    Cerdelga (eliglustat)
    Cemevit
    Cervarix [Human Papillomavirus Bivalent (Types 16 and 18) Vaccine, Recombinant
    Cetrotide
    Chantix (varenicline)
    Children's Advil (pediatric ibuprofen)
    Children's Motrin Cold
    Chloraprep (chlorhexidine gluconate)
    Cholbam (cholic acid)
    Cialis (tadalafil)
    Cimetadine Hydrochloride Oral Solution 300 mg/5 ml
    Cimetidine Hydrochloride Oral Solution
    Cimzia (certolizumab pegol)
    Cinryze (C1 Inhibitor (Human))
    Cipro (ciprofloxacin HCl)
    Cipro (ciprofloxacin) I.V. and Cipro (ciprofloxacin HCI) tablets
    Clarinex
    Clarithromycin (Biaxin)
    Claritin RediTabs (10 mg loratadine rapidly-disintegrating tablet)
    Claritin Syrup (loratadine)
    Claritin-D 24 Hour Extended Release Tablets (10 mg loratadine, 240 mg
    pseudoephedrine sulfate)
    Clemastine fumarate syrup
    Cleocin (clindamycin phosphate)
    Cleviprex (clevidipine)
    Climara
    Clindamycin phosphate topical gel
    Clindamycin Phosphate Topical Solution USP 1%
    Clolar (clofarabine)
    Clomipramine hydrochloride
    Clonazepam
    Coartem (artemether/lumefantrine)
    Colazal (balsalazide disodium)
    Colcrys (colchicine)
    Combivir
    Cometriq (cabozantinib)
    Complera (emtricitabine/rilpivirine/tenofovir disoproxil fumarate)
    Comtan
    Concerta
    Condylox Gel 0.5% (pokofilox)
    Confide
    Contrave (naltrexone HCl and bupropion HCl)
    Copaxone
    Corlanor (ivabradine)
    Corlopam
    Corvert Injection (ibutilide fumarate injection)
    Cosentyx (secukinumab)
    Cosopt
    Covera-HS (verapamil)
    Cresemba (isavuconazonium sulfate)
    Crestor (rosuvastatin calcium)
    Crinone 8% (progesterone gel)
    Crixivan (Indinavir sulfate)
    Curosurf
    Cuvposa (glycopyrrolate)
    Cycloset, bromocriptine mesylate
    Cylert
    Cymbalta (duloxetine)
    Cyramza (ramucirumab)
    Cystaran (cysteamine hydrochloride)
    Dacogen (decitabine)
    Daklinza (daclatasvir)
    Daliresp (roflumilast)
    Dalvance (dalbavancin)
    Daptacel
    Degarelix (degarelix for injection)
    DentiPatch (lidocaine transoral delivery system)
    Depakote (divalproex sodium)
    Depakote ER (divalproex sodium)
    Dermagraft-TC
    Desmopressin Acetate (DDAVP)
    Desonate (desonide)
    Detrol (tolterodine tartrate)
    Detrol LA (tolterodine tartrate)
    Diclegis (doxylamine succinate + pyridoxine hydrochloride DR tablets)
    Differin (adapalene gel) Gel, 0.1%
    Dificid (fidaxomicin)
    Diltiazem HCL, Extended-Release Capsules
    Diovan (valsartan)
    Diovan HCT (valsartan)
    Ditropan XL (oxybutynin chloride)
    Doribax (doripenem)
    Dostinex Tablets (cabergoline tablets)
    Doxil (doxorubicin HCl liposome injection)
    Droxia
    Duavee (conjugated estrogens/bazedoxifene)
    Duexis (ibuprofen and famotidine)
    Dulera (mometasone furoate + formoterol fumarate dihydrate)
    DuoNeb (albuterol sulfate and ipratropium bromide)
    Duopa (carbidopa and levodopa) enteral suspension
    Durezol (difluprednate)
    Dutasteride
    Dyloject (diclofenac sodium) Injection
    Dymista (azelastine hydrochloride and fluticasone propionate)
    Dynabac
    DynaCirc CR
    Edarbi (azilsartan medoxomil)
    Edarbyclor (azilsartan medoxomil and chlorthalidone)
    EDEX
    Edluar (zolpidem tartrate)
    Edurant (rilpivirine)
    Effexor (venlafaxin HCL)
    Effexor XR (venlafaxin HCI)
    Efient (prasugrel)
    Egrifta (tesamorelin for injection)
    Elaprase (idursulfase)
    Elelyso (taliglucerase alfa)
    Elestrin (estradiol gel)
    Elidel
    Eligard (leuprolide acetate)
    Eliquis (apixaban)
    Elitek (rasburicase)
    Ellence
    Elliotts B Solution (buffered intrathecal electrolyte/dextrose injection)
    Elmiron (pentosan polysulfate sodium)
    Eloctate [Antihemophilic Factor (Recombinant), Fc Fusion Protein]
    Eloxatin (oxaliplatin/5-fluorouracil/leucovorin)
    Embeda (morphine sulfate and naltrexone hydrochloride)
    Emend (aprepitant)
    Enbrel (etanercept)
    Entereg (alvimopan)
    Entocort EC (budesonide)
    Entresto (sacubitril and valsartan)
    Entyvio (vedolizumab)
    Envarsus XR (tacrolimus extended-release)
    Epanova (omega-3-carboxylic acids)
    Epivir (lamivudine)
    Eraxis (anidulafungin)
    Erbitux (cetuximab)
    Erivedge (vismodegib)
    Erwinaze (asparaginase Erwinia chrysanthemi)
    Esbriet (pirfenidone)
    Esclim
    Estradiol tablets
    Estradiol Transdermal System
    Estratab (.3 mg)
    EstroGel (estradiol gel 0.06%)
    Estrostep (norethindrone acetate and ethinyl estradiol)
    Ethyol (amifostine)
    Etodolac
    Eulexin (flutamide)
    Evamist (estradiol)
    Evista (raloxifene hydrochloride)
    Evotaz (atazanavir and cobicistat)
    Evoxac
    Exalgo (hydromorphone hydrochloride) extended release
    Excedrin Migraine
    Exelon (rivastigmine tartrate)
    Exparel (bupivacaine liposome injectable suspension)
    Extavia (Interferon beta-l b)
    Extina (ketoconazole)
    Eylea (aflibercept)
    Fabrazyme (agalsidase beta)
    Famvir (famciclovir)
    Fanapt (iloperidone)
    Farxiga (dapagliflozin)
    Farydak (panobinostat)
    Faslodex (fulvestrant)
    Femara (letrozole)
    Femhrt Tablets
    FemPatch
    Femstat 3 (butoconazole nitrate 2%)
    FEMSTAT One
    Fenofibrate
    Feraheme (ferumoxytol)
    Feridex I.V.
    Ferriprox (deferiprone)
    Ferrlecit
    Fertinex (urofollitropin for injection, purified)
    Fetzima (levomilnacipran)
    Finacea (azelaic acid) Gel, 15%
    Finevin
    Firazyr (icatibant)
    Flagyl ER
    FLOMAX
    Flonase Nasal Spray
    Flovent Rotadisk
    Floxin otic
    Floxin Tablets (ofloxacin tablets)
    Flublok (seasonal influenza vaccine)
    Flucelvax, Influenza Virus Vaccine
    FluMist (Influenza Virus Vaccine)
    Fluzone Preservative-free
    Focalin (dexmethylphenidate HCl)
    Follistim (TM) (follitropin beta for injection)
    Folotyn (pralatrexate injection)
    Foradil Aerolizer (formoterol fumarate inhalation powder)
    Forteo (teriparatide)
    Fortesta (testosterone gel)
    Fortovase
    Fosamax (alendronate sodium)
    Fosrenol, lanthanum carbonate
    Fragmin
    Frova (frovatriptan succinate)
    Fulyzaq (crofelemer)
    Fusilev (levoleucovorin)
    Fuzeon (enfuvirtide)
    Fycompa (perampanel)
    Galzin (zinc acetate)
    Gardasil (quadrivalent human papillomavirus (types 6, 11, 16, 18) recombinant vaccine)
    Gastrocrom Oral Concentrate (cromolyn sodium)
    GastroMARK
    Gattex (teduglutide)
    Gazyva (obinutuzumab)
    Gelnique (oxybutynin chloride)
    Gemzar (gemcitabine HCL)
    Generic Transdermal Nicotine Patch
    Genotropin (somatropin) injection
    Genotropin (somatropin) lyophilized powder
    Geodon (ziprasidone mesylate)
    Geref (sermorelin acetate for injection)
    Gilenya (fingolimod)
    Gilotrif (afatinib)
    Gleevec (imatinib mesylate)
    Gliadel Wafer (polifeprosan 20 with carmustine implant)
    Glipizide Tablets
    Glucagon
    Glyburide Tablets
    Glyset (miglitol)
    Gonal-F (follitropin alfa for injection)
    Gralise (gabapentin)
    Grastek (Timothy Grass Pollen Allergen Extract)
    Halaven (eribulin mesylate)
    Harvoni (ledipasvir and sofosbuvir)
    Havrix
    Hectorol (Doxercalciferol) Injection
    Hepsera (adefovir dipivoxil)
    Herceptin
    Herceptin (trastuzumab)
    Hetlioz (tasimelteon)
    Hiberix (Haemophilus b Conjugate Vaccine; Tetanus Toxoid Conjugate)
    Horizant (gabapentin enacarbil)
    Humalog (insulin lispro)
    Humatrope (somatropin [rDNA origin] for injection)
    Humira (adalimumab)
    Hycamtin (topotecan hydrochloride)
    HyQvia [Immune Globulin Infusion 10% (Human) with Recombinant Human
    Hyaluronidase]
    Iamin
    Ibrance (palbociclib)
    Iclusig (ponatinib)
    Ilaris (canakinumab)
    Imagent (perflexane lipid microspheres)
    Imbruvica (ibrutinib)
    Imitrex (sumatriptan) injection and tablets
    Imitrex (sumatriptan) nasal spray
    Impavido (miltefosine)
    Incivek (telaprevir)
    Increlex (mecasermin)
    Incruse Ellipta (umeclidinium inhalation powder)
    Infasurf
    INFERGEN (interferon alfacon-1)
    Inform HER-2/neu breast cancer test
    Injectafer (ferric carboxymaltose injection)
    Inlyta (axitinib)
    Innohep (tinzaparin sodium) injectable
    Inspra (eplerenone tablets)
    Integrilin
    Intelence (etravirine)
    Intermezzo (zolpidem tartrate sublingual tablet)
    Interstim Continence Control Therapy
    Intron A (Interferon alfa-2b, recombinant)
    Intuniv (guanfacine extended-release)
    Invanz
    Invega (paliperidone)
    Invirase (saquinavir)
    Invokana (canagliflozin)
    Iontocaine
    Iressa (gefitinib)
    Isentress (raltegravir)
    Istodax (romidepsin)
    IvyBlock
    Ixempra (ixabepilone)
    Ixiaro (Japanese Encephalitis Vaccine, Inactivated, Adsorbed)
    Jakafi (ruxolitinib)
    Jalyn (dutasteride + tamsulosin)
    Januvia (sitagliptin phosphate)
    Jardiance (empagliflozin)
    Jentadueto (linagliptin plus metformin hydrochloride)
    Jetrea (ocriplasmin)
    Jevtana (cabazitaxel)
    Jublia (efinaconazole) 10% topical gel
    Juvisync (sitagliptin and simvastatin)
    Juxtapid (lomitapide)
    Kadcyla (ado-trastuzumab emtansine)
    Kadian
    Kalbitor (ecallantide)
    Kaletra Capsules and Oral Solution
    Kalydeco (ivacaftor)
    Kapvay (clonidine hydrochloride)
    Kcentra (Prothrombin Complex Concentrate)
    Kengreal (cangrelor)
    Keppra
    Kerydin (tavaborole)
    Ketek (telithromycin)
    Ketoprofen
    Keytruda (pembrolizumab)
    Kineret
    Kineret, anakinra
    Klaron (sodium sulfacet amide lotion) Lotion, 10%
    Kogenate FS (Antihemophilic Factor Recombinant)
    Korlym (mifepristone)
    Krystexxa (pegloticase)
    Kuvan (sapropterin dihydrochloride)
    Kybella (deoxycholic acid)
    Kynamro (mipomersen sodium)
    Kyprolis (carfilzomib)
    Kytril (granisetron) solution
    Kytril (granisetron) tablets
    Lamictal (lamotrigine) Chewable Dispersible Tablets
    Lamictal Chewable Dispersible Tablets
    Lamisil (terbinafine hydrochloride) Dermagel, 1%
    Lamisil (terbinafine hydrochloride) Solution, 1%
    Lamisil (terbinafine hydrochloride) Tablets
    Lamisil Solution, 1%
    Lantus (insulin glargine [rDNA origin] injection)
    Latuda (lurasidone)
    Lazanda (fentanyl citrate) nasal spray
    Lemtrada (alemtuzumab)
    Lenvima (lenvatinib)
    Lescol (fluvastatin sodium)
    Lescol (fluvastatin sodium) capsules, Rx
    Lescol XL (fluvastatin sodium) tablet, extended release
    Letairis (ambrisentan)
    Leukine (sargramostim)
    Levaquin
    Levitra (vardenafil)
    Levo-T (levothyroxine sodium)
    Levoxyl
    Lexapro (escitalopram oxalate)
    Lexiva (fosamprenavir calcium)
    Lexxel (enalapril maleate-felodipine ER)
    Lidoderm Patch (lidocaine patch 5%)
    Linzess (linaclotide)
    Lipitor (atorvastatin calcium)
    Liptruzet (ezetimibe and atorvastatin)
    Lithobid (Lithium Carbonate)
    Livalo (pitavastatin)
    Lo Minastrin, (norethindrone acetate, ethinyl estradiol, ferrous fumarate)
    Lodine (etodolac)
    Lodine XL (etodolac)
    Lotemax
    Lotrisone (clotrimazole/betamethasone diproprionate) lotion
    Lotronex (alosetron HCL) Tablets
    Lovenox (enoxaparin sodium) Injection
    Lucentis (ranibizumab injection)
    Lucentis (ranibizumab)
    Lumigan (bimatoprost ophthalmic solution)
    Lunesta (eszopiclone)
    Lupron Depot (leuprolide acetate for depot suspension)
    Lusedra (fospropofol disodium)
    Lustra
    LUVOX (fluvoxamine maleate)
    Luxiq (betamethasone valerate) Foam
    Luzu (luliconazole) Cream 1%
    Lynparza (olaparib)
    Lyrica (pregabalin)
    Lysteda (tranexamic acid)
    Macugen (pegaptanib)
    Makena (hydroxyprogesterone caproate injection)
    Malarone (atovaquone; proguanil hydrochloride) Tablet
    Marplan Tablets
    Marqibo (vinCRIStine sulfate LIPOSOME injection)
    Mavik (trandolapril)
    Maxalt
    Mekinist (trametinib)
    Mentax (1% butenafine HCl cream)
    Menveo (meningitis vaccine)
    MERIDIA
    Merrem I.V. (meropenem)
    Mesnex
    Metadate CD
    Metaglip (glipizide/metformin HCl)
    Metaprotereol Sulfate Inhalation Solution, 5%
    Metozolv ODT (metoclopramide hydrochloride)
    MetroLotion
    Metronidazole 1.3% Vaginal Gel
    Mevacor (lovastatin) tablets
    Miacalcin (calcitonin-salmon) Nasal Spray
    Micardis (telmisartan)
    Micardis HCT (telmisartan and hydrochlorothiazide)
    Microzide (hydrochlorothiazide)
    Migranal
    Minoxidil Topical Solution 2% for Women
    Miraluma test
    Mirapex
    Mircera (methoxy polyethylene glycol-epoetin beta)
    Mircette
    Mirena (levonorgestrel-releasing intrauterine system)
    Mirvaso (brimonidine)
    Mobic (meloxicam) Tablets
    Monistat 3 (miconazole nitrate)
    Monurol
    Movantik (naloxegol)
    Moxatag (amoxicillin)
    Mozobil (plerixafor injection)
    Multaq (dronedarone)
    Muse
    Myalept (metreleptin for injection)
    Mylotarg (gemtuzumab ozogamicin)
    Myobloc
    Myozyme (alglucosidase alfa)
    Myrbetriq (mirabegron)
    Naglazyme (galsulfase)
    Naltrexone Hydrochloride Tablets
    Namenda (memantine HCl)
    Namzaric (memantine hydrochloride extended-release + donepezil hydrochloride)
    Naprelan (naproxen sodium)
    Nasacort AQ (triamcinolone acetonide) Nasal Spray
    NasalCrom Nasal Spray
    Nascobal Gel (Cyanocobalamin, USP)
    Nasonex Nasal Spray
    Natazia (estradiol valerate + dienogest)
    Natazia (estradiol valerate and estradiol valerate/dienogest)
    Natesto, (testosterone) nasal gel
    Natpara (parathyroid hormone)
    Natrecor (nesiritide)
    Nesina (alogliptin)
    Neulasta
    Neumega
    Neupogen
    Neupro (Rotigotine Transdermal System)
    Neupro (rotigotine)
    Neurontin (gabapentin)
    Neurontin (gabapentin) oral solution
    Neutroval (tbo-filgrastim)
    Nexavar (sorafenib)
    Nexium (esomeprazole magnesium)
    Niaspan
    NicoDerm CQ
    Nicorette (nicotine polacrilex)
    Nicotrol nasal spray
    Nicotrol transdermal patch
    Nitrostat (nitroglycerin) Tablets
    Nolvadex
    NORCO tablets (Hydrocodone Bitartrate/Acetaminophen 10 mg/325 mg)
    Norditropin (somatropin (rDNA origin) for injection)
    Noritate
    Normiflo
    Northera (droxidopa)
    Norvir (ritonavir)
    Novantrone (mitoxantrone hydrochloride)
    NovoLog (insulin aspart)
    Novolog Mix 70/30
    Novothyrox (levothyroxine sodium)
    Noxafil (posaconazole)
    Nplate (romiplostim)
    Nucynta (tapentadol)
    Nuedexta (dextromethorphan hydrobromide and quinidine sulfate)
    Nulojix (belatacept)
    Nutropin (somatropin-rDNA origin)
    NuvaRing
    Nuvigil (armodafmil)
    Nymalize (nimodipine)
    Obizur [Antihemophilic Factor (Recombinant), Porcine Sequence]
    Ocuflox (ofloxacin opthalmic solution) 0.3%
    OcuHist
    Odomzo (sonidegib)
    Ofev (nintedanib)
    Oleptro (trazodone hydrochloride)
    Olysio (simeprevir)
    Omidria (phenylephrine and ketorolac injection)
    Omnicef
    Omontys (peginesatide)
    Onfi (clobazam)
    Onglyza (saxagliptin)
    Onsolis (fentanyl buccal)
    Opdivo (nivolumab)
    Opsumit (macitentan)
    Oral Cytovene
    Oralair (Sweet Vernal, Orchard, Perennial Rye, Timothy and Kentucky Blue Grass
    Mixed Pollens Allergen Extract)
    Oravig (miconazole)
    Orbactiv (oritavancin)
    Orencia (abatacept)
    Orfadin (nitisinone)
    Orkambi (lumacaftor and ivacaftor)
    Ortho Evra
    Ortho Tri-Cyclen Tablets (norgestimate/ethinyl estradiol)
    Ortho-Prefest
    OsmoCyte Pillow Wound Dressing
    Osphena (ospemifene)
    Otezla (apremilast)
    Ovidrel (gonadotropin, chorionic human recombinant)
    Oxecta (oxycodone HCl)
    Oxtellar XR (oxcarbazepine extended release)
    Oxycodone and Aspirin
    Oxycodone with Acetaminophen 5 mg/325 mg
    OxyContin (oxycodone HCl controlled-release)
    Oxytrol (oxybutynin transdermal system)
    Ozurdex (dexamethasone)
    Pancreaze (pancrelipase)
    Panretin Gel
    Patanase (olopatadine hydrochloride)
    Paxil (paroxetine hydrochloride)
    Paxil CR (paroxetine hydrochloride)
    Pediarix Vaccine
    Pegasys (peginterferon alfa-2a)
    Peg-Intron (peginterferon alfa-2b)
    Pennsaid (diclofenac sodium topical solution)
    Pentoxifylline
    Pepcid Complete
    Periostat (doxycycline hyclate)
    Perjeta (pertuzumab)
    PhosLo
    Photodynamic Therapy
    Photofrin
    Picato (ingenol mebutate) gel
    Pindolol
    Plavix (clopidogrel bisulfate)
    Plegridy (peginterferon beta-1a)
    Plenaxis (abarelix for injectable suspension)
    Pomalyst (pomalidomide)
    Posicor
    Potiga (ezogabine)
    Pradaxa (dabigatran etexilate mesylate)
    Praluent (alirocumab)
    Pramipexole
    Prandin
    Pravachol (pravastatin sodium)
    Precose (acarbose)
    Premarin (conjugated estrogens)
    Prempro
    Prempro & Premphase (conjugated estrogens/medroxyprogesterone acetate tablets)
    Prestalia (perindopril arginine and amlodipine besylate)
    PREVACID(R) (lansopraxole)
    PREVEN; Emergency Contraceptive Kit
    Prevnar 13 (Pneumococcal 13-valent Conjugate Vaccine)
    Prevpac
    Prezcobix (darunavir and cobicistat)
    Prezista (darunavir)
    Priftin
    Prilosec (omeprazole)
    Prilosec (omeprazole)/Biaxin (clarithromycin) Combination Therapy
    Prinivil or Zestril (Lisinopril)
    ProAmatine (midodrine)
    Procanbid (procainamide hydrochloride extended-release tablets)
    Prochloroperazine
    Prochlorperazine
    Procysbi (cysteamine bitartrate)
    Prograf
    Proleukin
    Prolia (denosumab)
    Promacta (eltrombopag)
    Prometrium
    Propecia
    Proscar
    Protonix (pantoprazole sodium) Delayed Release Tablets
    Protonix (pantoprazole sodium) Delayed-Release Tablets
    Protonix (pantoprazole sodium) Intravenous Formulation
    Protopic (tacrolimus) ointment
    Provenge (sipuleucel-T)
    Proventil HFA Inhalation Aerosol
    Prozac Weekly (fluoxetine HCl)
    Pulmozyme (dornase alfa)
    Qnasl (beclomethasone dipropionate) nasal aerosol
    Qsymia (phentermine + topiramate extended-release)
    Quadramet (Samarium Sm 153 Lexidronam Injection)
    Quartette (levonorgestrel/ethinyl estradiol and ethinyl estradiol)
    Qudexy XR (topiramate)
    Quillivant XR (methylphenidate hydrochloride)
    Quixin (levofloxacin)
    Qutenza (capsaicin)
    Qvar (beclomethasone dipropionate)
    Ragwitek (Short Ragweed Pollen Allergen Extract)
    Ranexa (ranolazine)
    Ranitidine Capsules
    Ranitidine Tablets
    Rapamune (sirolimus) oral solution
    Rapamune (sirolimus) Tablets
    Rapivab (peramivir injection)
    Rapion
    Ravicti (glycerol phenylbutyrate)
    Raxar (grepafloxacin)
    Rayos (prednisone) delayed-release tablets
    Rebetol (ribavirin)
    REBETRON (TM) Combination Therapy
    Rebif (interferon beta-1a)
    Reclast (zoledronic acid)
    Rectiv (nitroglycerin) ointment 0.4%
    Redux (dexfenfluramine hydrochloride)
    Refludan
    REGRANEX (becaplermin) Gel
    Relenza
    Relpax (eletriptan hydrobromide)
    Remeron (Mirtazapine)
    Remeron SolTab (mirtazapine)
    Remicade (infliximab)
    Reminyl (galantamine hydrobromide)
    Remodulin (treprostinil)
    Renagel (sevelamer hydrochloride)
    RenaGelRenagel (sevelamer hydrochloride)
    Renova (tretinoin emollient cream)
    Renvela (sevelamer carbonate)
    ReoPro
    Repatha (evolocumab)
    REPRONEX(menotropins for injection, USP)
    Requip (ropinirole hydrochloride)
    Rescriptor Tablets (delavirdine mesylate tablets)
    Rescula (unoprostone isopropyl ophthalmic solution) 0.15%
    RespiGam (Respiratory Syncitial Virus Immune Globulin Intravenous)
    Restasis (cyclosporine ophthalmic emulsion)
    Retavase (reteplase)
    Retin-A Micro (tretinoin gel) microsphere, 0.1%
    Revlimid (lenalidomide)
    Rexulti (brexpiprazole)
    Reyataz (atazanavir sulfate)
    Rhinocort Aqua Nasal Spray
    Rid Mousse
    Rilutek (riluzole)
    Risperdal Oral Formulation
    Ritalin LA (methylphenidate HCl)
    Rituxan
    Rixubis (Coagulation Factor IX (Recombinant)]
    Rocephin
    Rotarix (Rotavirus Vaccine, Live, Oral)
    Rotateq (rotavirus vaccine, live oral pentavalent)
    Rozerem (ramelteon)
    Ruconest (C1 esterase inhibitor [recombinant])
    Rytary (carbidopa and levodopa) extended-release capsules
    Rythmol
    Sabril (vigabatrin)
    Saizen
    Salagen Tablets
    Samsca (tolvaptan)
    Sanctura (trospium chloride)
    Sancuso (granisetron)
    Saphris (asenapine)
    Savaysa (edoxaban)
    Savella (milnacipran hydrochloride)
    Saxenda (liraglutide [rDNA origin] injection)
    Sclerosol Intrapleural Aerosol
    Seasonale, Lo Seasonale, Seasonique (ethinylestradiol + levonorgestrel)
    SecreFlo (secretin)
    Selegiline tablets
    Self-examination breast pad
    Selzentry (maraviroc)
    Sensipar (cinacalcet)
    Seprafilm
    Serevent
    Seroquel (R) (quetiapine fumarate) Tablets
    Signifor (pasireotide diaspartate)
    Signifor LAR (pasireotide)
    Silenor (doxepin)
    Simponi (golimumab)
    Simulect
    Singulair
    Sirturo (bedaquiline)
    Sitavig (acyclovir) buccal tablets
    Sivextro (tedizolid phosphate)
    Skelid (tiludronate disodium)
    Skin Exposure Reduction Paste Against Chemical Warfare Agents (SERPACWA)
    Sklice (ivermectin) lotion
    Soliris (eculizumab)
    Somatuline Depot (lanreotide acetate)
    Somavert (pegvisomant)
    Sonata
    Soolantra (ivermectin) cream, 1%
    Sovaldi (sofosbuvir)
    Spectracef
    Spiriva HandiHaler (tiotropium bromide)
    SPORANOX (itraconazole)
    Sprix (ketorolac tromethamine)
    Sprycel (dasatinib)
    Stavzor (valproic acid delayed release)
    Stelara (ustekinumab)
    Stendra (avanafil)
    Stiolto Respimat (tiotropium bromide and olodaterol)
    Stivarga (regorafenib)
    Strattera (atomoxetine HCl)
    Stribild (elvitegravir, cobicistat, emtricitabine, tenofovir disoproxil fumarate)
    Striverdi Respimat (olodaterol)
    Stromectol (ivermectin)
    Subsys (fentanyl sublingual spray)
    Subutex/Suboxone (buprenorphine/naloxone)
    Sulfamylon
    Supartz
    Supprelin LA (histrelin acetate)
    Surfaxin (lucinactant)
    Sustiva
    Sutent (sunitinib malate)
    Sutent (sunitinib)
    Sylatron (peginterferon alfa-2b)
    Sylvant (siltuximab)
    Symlin (pramlintide)
    Synagis
    Synercid I.V.
    Synjardy (empagliflozin and metformin hydrochloride)
    Synribo (omacetaxine mepesuccinate)
    Synthroid (levothyroxine sodium)
    Synvisc, Synvisc-One (Hylan GF 20)
    Tafinlar (dabrafenib)
    Tamiflu capsule
    Tanzeum (albiglutide)
    Tarceva (erlotinib, OSI 774)
    Targiniq ER (oxycodone hydrochloride + naloxone hydrochloride) extended-release
    tablets
    Tasigna (nilotinib hydrochloride monohydrate)
    Tasmar
    Tavist (clemastine fumarate)
    Taxol
    Taxotere (Docetaxel)
    Tazorac topical gel
    Tecfidera (dimethyl fumarate)
    Technivie, (ombitasvir, paritaprevir and ritonavir)
    Teczem (enalapril maleate/diltiazem malate)
    Teflaro (ceftaroline fosamil)
    Tegretol (carbamazepine)
    Tegretol XR (carbamazepine)
    Tekamlo (aliskiren + amlodipine)
    Tekturna (aliskiren)
    Temodar
    Tequin
    Testim
    Testoderm TTS CIII
    Teveten (eprosartan mesylate plus hydrochlorothiazide)
    Teveten (eprosartan mesylate)
    Thalomid
    Tiazac (diltiazem hydrochloride)
    Tikosyn Capsules
    Tilade (nedocromil sodium)
    Timentin
    Tindamax, tinidazole
    Tivicay (dolutegravir)
    Tivorbex (indomethacin)
    Tobi
    Tolmetin Sodium
    Topamax (topiramate)
    Toprol-XL (metoprolol succinate)
    Torisel (temsirolimus)
    Toviaz (fesoterodine fumarate)
    Tracleer (bosentan)
    Tradjenta (linagliptin)
    Travatan (travoprost ophthalmic solution)
    Trazadone 150 mg
    Treanda (bendamustine hydrochloride)
    Trelstar Depot (triptorelin pamoate)
    Trelstar LA (triptorelin pamoate)
    Tretten (Coagulation Factor XIII A-Subunit [Recombinant])
    Tribenzor (olmesartan medoxomil + amlodipine + hydrochlorothiazide)
    Tricor (fenofibrate)
    Trileptal (oxcarbazepine) Tablets
    Trilipix (fenofibric acid)
    Tri-Nasal Spray (triamcinolone acetonide spray)
    Tripedia (Diptheria and Tetanus Toxoids and Acellular Pertussis Vaccine Absorbed)
    Trisenox (arsenic trioxide)
    Triumeq (abacavir, dolutegravir, and lamivudine)
    Trivagizole 3 (clotrimazole) Vaginal Cream
    Trivora-21 and Trivora-28
    Trizivir (abacavir sulfate; lamivudine; zidovudine AZT) Tablet
    Trokendi XR (topiramate)
    Trovan
    Trulicity (dulaglutide)
    Tudorza Pressair (aclidinium bromide inhalation powder)
    Twinrix
    Tygacil (tigecycline)
    Tykerb (lapatinib)
    Tysabri (natalizumab)
    Tyvaso (treprostinil)
    Tyzeka (telbivudine)
    Uceris (budesonide)
    Uloric (febuxostat)
    Ultracet (acetaminophen and tramadol HCl)
    UltraJect
    Ultresa (pancrelipase) delayed-release capsules
    Unituxin (dinutuximab)
    UroXatral (alfuzosin HCl extended-release tablets)
    Urso
    UVADEX Sterile Solution
    Valchlor (mechlorethamine) gel
    Valcyte (valganciclovir HCl)
    Valstar
    Valtrex (valacyclovir HCl)
    Vancenase AQ 84 mcg Double Strength
    Vanceril 84 mcg Double Strength (beclomethasone dipropionate, 84 mcg) Inhalation
    Aerosol
    Vandetanib (vandetanib)
    Vaprisol (conivaptan)
    Varithena (polidocanol injectable foam)
    VariZIG, Varicella Zoster Immune Globulin (Human)
    Varubi (rolapitant)
    Vascepa (icosapent ethyl)
    Vectibix (panitumumab)
    Velcade (bortezomib)
    Veltin (clindamycin phosphate and tretinoin)
    Venofer (iron sucrose injection)
    Ventolin HFA (albuterol sulfate inhalation aerosol)
    Veramyst (fluticasone furoate)
    Verapamil
    Verdeso (desonide)
    Veregen (kunecatechins)
    VERSED (midazolam HCI)
    Vesicare (solifenacin succinate)
    Vfend (voriconazole)
    Viadur (leuprolide acetate implant)
    Viagra
    Vibativ (telavancin)
    Viberzi (eluxadoline)
    Victoza (liraglutide)
    Victrelis (boceprevir)
    Vidaza (azacitidine)
    Videx (didanosine)
    Viekira Pak (ombitasvir, paritaprevir, ritonavir and dasabuvir) tablets
    Viibryd (vilazodone hydrochloride)
    Vimizim (elosulfase alfa)
    Vimovo (naproxen + esomeprazole)
    Vimpat (lacosamide)
    Viokace (pancrelipase) tablets
    Vioxx (rofecoxib)
    VIRACEPT (nelfinavir mesylate)
    Viramune (nevirapine)
    Viread (tenofovir disoproxil fumarate)
    Viroptic
    Visicol Tablet
    Visipaque (iodixanol)
    Vistide (cidofovir)
    Visudyne (verteporfin for injection)
    Vitrasert Implant
    Vitravene Injection
    Vivelle (estradiol transdermal system)
    Vivelle-Dot (estradiol transdermal system)
    Vivitrol (naltrexone for extended-release injectable suspension)
    Vogelxo (testosterone) gel
    Voraxaze (glucarpidase)
    Votrient (pazopanib)
    Vpriv (velaglucerase alfa for injection)
    Vyvanse (Lisdexamfetamine Dimesylate)
    Warfarin Sodium tablets
    Welchol (colesevelam hydrochloride)
    Western blot confirmatory device
    Wilate (von Willebrand Factor/Coagulation Factor VIII Complex (Human)
    Xalkori (crizotinib)
    Xarelto (rivaroxaban)
    Xartemis XR (oxycodone hydrochloride and acetaminophen) extended release
    Xeljanz (tofacitinib)
    Xeloda
    Xenazine (tetrabenazine)
    Xenical/Orlistat Capsules
    Xeomin (incobotulinumtoxinA)
    Xgeva (denosumab)
    Xiaflex (collagenase clostridium histolyticum)
    Xifaxan (rifaximin)
    Xigduo XR (dapagliflozin + metformin hydrochloride)
    Xigris (drotrecogin alfa [activated])
    Xofigo (radium Ra 223 dichloride)
    Xolair (omalizumab)
    Xopenex
    Xtandi (enzalutamide)
    Xtoro (finafloxacin otic suspension) 0.3%
    Xyrem (sodium oxybate)
    Xyzal (levocetirizine dihydrochloride)
    Yasmin (drospirenone/ethinyl estradiol)
    Yervoy (ipilimumab)
    ZADITOR
    Zagam (sparfloxacin) tablets
    Zaltrap (ziv-aflibercept)
    Zanaflex (tizanidine hydrochloride)
    Zantac 75 Efferdose
    Zelboraf (vemurafenib)
    Zelnorm (tegaserod maleate) Tablets
    Zemaira (alpha1-proteinase inhibitor)
    Zemplar
    Zenapax
    Zenpep (pancrelipase)
    Zerbaxa (ceftolozane + tazobactam)
    Zerit (stavudine)
    Zevalin (ibritumomab tiuxetan)
    Zingo (lidocaine hydrochloride monohydrate)
    Zioptan (tafluprost ophthalmic solution)
    Ziprasidone (ziprasidone hydrochloride)
    Zipsor (diclofenac potassium)
    Zirgan (ganciclovir ophthalmic gel)
    Zithromax (azithromycin)
    Zocor
    Zofran
    Zohydro ER (hydrocodone bitartrate) Extended-Release Capsules
    Zoladex (10.8 mg goserelin acetate implant)
    Zoloft (sertraline HCl)
    Zometa (zoledronic acid)
    Zomig (zolmitriptan)
    Zonegran (zonisamide) Capsules
    Zontivity (vorapaxar)
    Zortress (everolimus)
    Zosyn (sterile piperacillin sodium/tazobactam sodium)
    Zubsolv (buprenorphine and naloxone)
    Zuplenz (ondansetron oral soluble film)
    Zyban Sustained-Release Tablets
    Zyclara (imiquimod)
    Zydelig (idelalisib)
    Zyflo (Zileuton)
    Zykadia (ceritinib)
    Zymaxid (gatifloxacin ophthalmic solution)
    Zyprexa
    Zyrtec (cetirizine HCl)
    Zytiga (abiraterone acetate)
  • Table 4 lists sample drugs and their side effects. The listed drugs and their side effects highlight a number side effects that can be used for the development of the Patient Specific Dispensing Algorithm. The following approved drugs in Table 4 and in the following marketed drug compounds and drug compounds in development are encompassed in the embodiment of the invention by reference. Marketed drug compounds of interest are also listed in: Goodman & Gilman's, The Pharmacological Basis of Therapeutics (12th Ed) (Goodman et al. eds) (McGraw-Hill) (2011); and 2015 Physician's Desk Reference. Drug compounds in development that are of interest are also listed in: Cortellis™ Competitive Intelligence by Thomson Reuters; Adis R&D; and Pharmaprojects by Citeline. The drug The listing for each drug includes by definition each drug's respective indication(s), strength, dosage form, route of administration, side effect profile, drug interactions, etc.
  • TABLE 4
    SAMPLE DRUGS AND THEIR SIDE EFFECTS
    Afinitor Common:
    Cardiovascular: Hypertension (tumors, 4% to 13%; kidney
    transplant, 30%; liver transplant, 17%), Peripheral edema (tumors,
    13% to 39%; kidney transplant, 45%; liver transplant, 18%)
    Dermatologic: Acne (tumors, 10% to 22%; transplant, 1% to less
    than 10%), Eczema (renal angiomyolipoma, 10%), Rash (tumors,
    5% to 59%)
    Endocrine metabolic: Dyslipidemia (kidney transplant, 15%),
    Hypercholesterolemia (tumors, 66% to 85%; kidney transplant,
    17%), Hyperlipidemia (kidney transplant, 21%; liver transplant,
    24%), Hypertriglyceridemia (tumors, 27% to 73%),
    Hypoalbuminemia (breast cancer, 33%), Hypophosphatemia
    (tumors, 9% to 49%; kidney transplant, 13%), Increased glucose
    level, All grades (tumors, 14% to 75%; kidney transplant, 12%)
    Gastrointestinal: Constipation (tumors, 10% to 14%; kidney
    transplant, 38%), Decrease in appetite (tumors, 6% to 30%;
    transplant, 1% to less than 10%), Diarrhea (tumors, 14% to 50%;
    kidney transplant, 19%; liver transplant, 19%), Nausea (tumors,
    16% to 29%; kidney transplant, 29%; liver transplant, 14%),
    Stomatitis (tumors, 44% to 78%; kidney transplant, 8%), Vomiting
    (tumors, 15% to 29%; kidney transplant, 15%)
    Hematologic: Anemia, All Grades (tumors, 41% to 86%; kidney
    transplant, 26%), Decreased lymphocyte count, All grades (tumors,
    20% to 54%), Partial thromboplastin time increased (subependymal
    giant cell astrocytoma, 72%), Thrombocytopenia, All grades
    (tumors, 19% to 54%; transplant, up to 10%)
    Hepatic: Alkaline phosphatase raised (tumors, 32% to 74%;
    transplant, 1% to less than 10%), ALT/SGPT level raised (tumors,
    18% to 51%), AST/SGOT level raised (tumors, 23% to 69%)
    Immunologic: Impaired wound healing (kidney transplant, 35%;
    liver transplant, 11%)
    Neurologic: Asthenia (tumors, 13% to 33%)
    Otic: Otitis media (renal angiomyolipoma, 6%)
    Psychiatric: Mental disorder (subependymal giant cell
    astrocytoma, 21%)
    Renal: Serum creatinine raised (tumors, 19% to 50%; kidney
    transplant, 18%), Urinary tract infectious disease (tumors, 5% to
    16%; kidney transplant, 22%)
    Reproductive: Amenorrhea (renal angiomyolipoma, 15%),
    Irregular periods (tumors, 10% to 11%), Menorrhagia (renal
    angiomyolipoma, 10%)
    Respiratory: Cough (tumors, 20% to 30%; kidney transplant, 7%),
    Dyspnea (tumors, 20% to 24%), Sinusitis (tumors, 3% to 6%),
    Upper respiratory infection (tumors, 11% to 31%; kidney
    transplant, 16%)
    Other: Fatigue (tumors, 14% to 45%; kidney transplant, 9%),
    Fever (tumors, 15% to 31%; kidney transplant, 19%; liver
    transplant, 13%)
    Serious:
    Cardiovascular: Pericardial effusion (Transplant, less than 1%)
    Hematologic: Anemia, Grade 3 or 4 (tumors, 6.6% to 15%),
    Decreased lymphocyte count, Grade 3 or 4 (tumors, 1% to 16%),
    Hemorrhage (renal cell carcinoma, 3%), Leukopenia (tumors, 37%
    to 58%; kidney transplant, 3%; liver transplant, 12%),
    Pancytopenia, All grades (transplant, 1% to less than 10%),
    Thrombosis, Thrombotic microangiopathy (Transplant, less than
    1%), Thrombotic thrombocytopenic purpura (Transplant, less than
    1%), Venous thromboembolism (transplant, 1% to less than 10%)
    Immunologic: Infectious disease (tumors, 37% to 50%; kidney
    transplant, 62%; liver transplant, 50%)
    Neurologic: Seizure (renal angiomyolipoma, 5%)
    Renal: Hemolytic uremic syndrome (Transplant, less than 1%),
    Renal failure (renal cell carcinoma, 3%), Thrombosis of renal
    artery (transplant, 1% to less than 10%)
    Respiratory: Interstitial lung disease (Less than 1%), Non-
    infectious pneumonia (Up to 19%), Pleural effusion (tumors, 7%),
    Pneumocystis pneumonia, Pneumonia (renal cell carcinoma, 6%),
    Pulmonary embolism (PNET, 2.5%; transplant, 1% to less than
    10%)
    Other: Angioedema (Transplant, up to 6.8%), Sepsis (tumors less
    than 1%; transplant, 1% to less than 10%)
    Ampyra Common
    Gastrointestinal: Abdominal pain (7%), Nausea (7% to 13%),
    Vomiting (13%)
    Musculoskeletal: Abnormal gait (5%), Backache (5%)
    Neurologic: Asthenia (7%), Dizziness (7%), Headache (7%),
    Insomnia (9%)
    Psychiatric: Anxiety (5%)
    Renal: Urinary tract infectious disease (12%)
    Serious
    Immunologic: Anaphylaxis, Hypersensitivity reaction
    Neurologic: Seizure
    Angeliq Common
    Gastrointestinal: Abdominal pain (3.6% to 6.5%)
    Neurologic: Headache (6%)
    Reproductive: Abnormal vaginal bleeding (3.6% to 14%), Pain of
    breast (3.3% to 17.9%)
    Serious
    Cardiovascular: Myocardial infarction
    Gastrointestinal: Disorder of gallbladder
    Hematologic: Deep venous thrombosis
    Neurologic: Cerebrovascular accident
    Ophthalmic: Thrombosis of retinal vein
    Reproductive: Breast cancer, Endometrial carcinoma, Ovarian
    cancer
    Respiratory: Pulmonary embolism
    Brisdelle Common
    Dermatologic: Diaphoresis (1% to 14%)
    Gastrointestinal: Constipation (4.9% to 16%), Diarrhea (7.9% to
    19.2%), Loss of appetite (2% to 9%), Nausea (up to 36.3%),
    Xerostomia (10.8% to 20.6%)
    Neurologic: Asthenia (2.9% to 22%), Dizziness (6% to 14%),
    Headache (psychiatric conditions, 17% to 18%; menopausal
    vasomotor symptoms, 6.3%), Insomnia (11% to 24%), Somnolence
    (12.7% to 24%), Tremor (up to 14.7%)
    Ophthalmic: Blurred vision (2% to 7.8%)
    Reproductive: Abnormal ejaculation (5.8% to 28%), Disorder of
    female genital organs (2% to 9%), Erectile dysfunction (1.9% to
    9%), Reduced libido (males, 6% to 15%; females, 0% to 9%)
    Serious
    Psychiatric: Depression, Exacerbation, Suicidal thoughts, Suicide
    Other: Serotonin syndrome
    Contrave Common:
    Gastrointestinal: Constipation (19.2%), Diarrhea (7.1%), Nausea
    (32.5%), Vomiting (10.7%), Xerostomia (8.1%)
    Neurologic: Dizziness (9.9%), Headache (17.6%), Insomnia (9.2%)
    Psychiatric: Anxiety (4.2%)
    Serious:
    Cardiovascular: Hypertension (3.2%), Increased heart rate,
    Myocardial infarction (Less than 2%)
    Dermatologic: Erythema multiforme (Rare), Stevens-Johnson
    syndrome (Rare)
    Endocrine metabolic: Hypoglycemia
    Gastrointestinal: Cholecystitis (Less than 2%), Hematochezia (Less
    than 2%)
    Hepatic: Hepatotoxicity
    Immunologic: Anaphylaxis, Delayed hypersensitivity disorder
    Musculoskeletal: Intervertebral disc prolapse (Less than 2%)
    Neurologic: Amnesia (Less than 2%), Seizure (0.1%)
    Ophthalmic: Angle-closure glaucoma
    Psychiatric: Depression (6.3% to 7.1%), Mania, Psychiatric
    symptom, Suicidal thoughts (0.03%)
    Renal: Infectious disorder of kidney (Less than 2%), Serum
    creatinine raised (Less than 2%)
    Respiratory: Pneumonia (Less than 2%)
    Daliresp Common:
    Endocrine metabolic: Weight decreased (7% to 20%)
    Gastrointestinal: Decrease in appetite (2.1%), Diarrhea (9.5%),
    Nausea (4.7%)
    Immunologic: Influenza (2.8%)
    Musculoskeletal: Backache (3.2%)
    Neurologic: Dizziness (2.1%), Headache (4.4%), Insomnia (2.4%)
    Serious:
    Psychiatric: Suicidal thoughts
    Doryx Common:
    Dermatologic: Rash (4%)
    Gastrointestinal: Diarrhea (3.3%), Loss of appetite, Nausea (8% to
    13.4%), Sensitive dentin, Sore gums, Vomiting (8.1%)
    Musculoskeletal: Myalgia (6.4%)
    Reproductive: Bacterial vaginosis (3.3%)
    Serious:
    Dermatologic: Drug hypersensitivity syndrome, Erythema
    multiforme, Photosensitivity, Stevens-Johnson syndrome, Toxic
    epidermal necrolysis
    Gastrointestinal: Clostridium difficile diarrhea
    Hepatic: Hepatotoxicity (Rare)
    Immunologic: Anaphylaxis, Superinfection
    Musculoskeletal: Arrest of bone development AND/OR growth
    Neurologic: Pseudotumor cerebri
    Ella Common:
    Gastrointestinal: Abdominal pain (8% to 15%), Nausea (12% to
    13%)
    Neurologic: Headache (18% to 19%)
    Equetro Common
    Cardiovascular: Hypotension
    Dermatologic: Pruritus (8%), Rash (7%)
    Gastrointestinal: Constipation (10%), Nausea (29%), Vomiting
    (18%), Xerostomia (8%)
    Neurologic: Asthenia (8%), Ataxia (15%), Dizziness (44%),
    Somnolence
    Ophthalmic: Blurred vision (6%), Nystagmus
    Serious
    Cardiovascular: Atrioventricular block, Cardiac dysrhythmia,
    Congestive heart failure, Eosinophilic myocarditis,
    Hypersensitivity, Syncope
    Dermatologic: Stevens-Johnson syndrome, Toxic epidermal
    necrolysis
    Endocrine metabolic: Hypocalcemia, Hyponatremia (4% to 21.7%),
    Water intoxication syndrome
    Gastrointestinal: Pancreatitis
    Hematologic: Agranulocytosis, Aplastic anemia, Bone marrow
    depression, Eosinophilia, Leukopenia, Pancytopenia,
    Thrombocytopenia
    Hepatic: Hepatitis, Hepatotoxicity, Liver failure, Vanishing bile
    duct syndrome
    Immunologic: Drug hypersensitivity syndrome
    Neurologic: Acute intermittent porphyria
    Renal: Azotemia, Renal failure
    Respiratory: Pulmonary hypersensitivity
    Other: Angioedema
    Gabitril Common:
    Dermatologic: Pruritus (2%)
    Gastrointestinal: Abdominal pain (5% to 7%), Nausea (11%)
    Neurologic: Asthenia (18% to 23%), Ataxia (5% to 9%), Confusion
    (5%), Disturbance in speech (4%), Dizziness (27 to 31%), Feeling
    nervous (10% to 14%), Insomnia (5% to 6%), Somnolence (18% to
    21%), Tremor (9% to 21%), Unable to concentrate (6% to 14%)
    Respiratory: Pharyngitis (7% to 8%)
    Serious:
    Dermatologic: Stevens-Johnson syndrome
    Neurologic: Seizure, in patients without epilepsy, Status
    epilepticus, Status epilepticus, in patients without a history of
    seizure
    Psychiatric: Suicidal thoughts
    Gilenya Common:
    Gastrointestinal: Abdominal pain (11%), Diarrhea (13%)
    Hepatic: Increased liver enzymes (All elevations
    (ALT/GGT/AST), 15%; up to 3 times ULN (ALT, AST), 14%; 5
    times ULN or greater (ALT, AST), 4.5%)
    Immunologic: Influenza (11%)
    Musculoskeletal: Backache (10%), Pain, In Extremity (10%)
    Neurologic: Headache (25%)
    Respiratory: Cough (12%), Sinusitis (11%)
    Serious:
    Cardiovascular: Atrioventricular block (up to 4.7%),
    Bradyarrhythmia (3%.)
    Dermatologic: Malignant melanoma
    Hematologic: Lymphocytopenia (Severe) (7%)
    Immunologic: Cryptococcosis, Herpesvirus infection (9%),
    Infectious disease (All infections, 72%; serious infections, 2.3%)
    Neurologic: Cryptococcal meningitis, Posterior reversible
    encephalopathy syndrome, Progressive multifocal
    leukoencephalopathy
    Ophthalmic: Macular retinal edema (0.5% to 1.5%)
    Gleevec Common:
    Cardiovascular: Edema
    Dermatologic: Night sweats (13% to 17%), Rash (Adult, 8.9% to
    38.1%; pediatric, acute lymphocytic leukemia, grade 3 or 4, 4%)
    Endocrine metabolic: Weight increased (5% to 32%)
    Gastrointestinal: Diarrhea (Adult, 25% to 59.3%; pediatric, acute
    lymphoblastic leukemia, grade 3 or 4, 9%), Nausea (Adults, 41.7%
    to 73%; pediatric, acute lymphoblastic leukemia, grade 3 or 4,
    16%), Vomiting (10.8% to 58%)
    Musculoskeletal: Arthralgia (8.8% to 40%), Cramp (28% to 62%),
    Musculoskeletal pain (Chronic myeloid leukemia, 20.5% to 49%),
    Myalgia (Adult, 9% to 33.2%; pediatric, acute lymphoblastic
    leukemia grade 3 or 4, 5%), Spasm (16.3% to 49%)
    Neurologic: Asthenia (12% to 21%), Dizziness (4.6% to 16%),
    Headache (8.2% to 36%), Insomnia (9.8% to 14%)
    Respiratory: Cough (13% to 27%), Nasopharyngitis (1% to 30.5%),
    Pain, Pharyngolaryngeal (Chronic myeloid leukemia, 18.1%),
    Pharyngitis (Chronic myeloid leukemia, 10% to 15%)
    Other: Fatigue (20% to 57%), Fever (6.2% to 41%), Influenza
    (Chronic myeloid leukemia, 0.8% to 13.8%), Rigor (10% to 12%)
    Serious:
    Cardiovascular: Cardiac tamponade, Cardiogenic shock,
    Congestive heart failure (0.1% to 1%)
    Dermatologic: Bullous eruption (0.1% to 1%), Erythema
    multiforme (0.01% to 0.1%), Stevens-Johnson syndrome (0.01% to
    0.1%), Toxic epidermal necrolysis
    Gastrointestinal: Gastrointestinal perforation, Pancreatitis (0.1% to
    1%)
    Hematologic: Anemia (Up to 42%), Febrile neutropenia (1% to
    10%), Hemorrhage (All grades, 1% to 53%; grade 3 or 4, 0% to
    19%), Neutropenia (Grade 3 or 4, 3.1% to 64%), Pancytopenia (1%
    to 10%), Thrombocytopenia (Chronic myeloid leukemia (CML),
    grade 3, 8.5% to 30%; CML, grade 4, up to 33%;
    dermatofibrosarcoma protuberans (oral route): 17%)
    Hepatic: ALT/SGPT level raised (grade 3 and above, up to 7%),
    Ascites (0.1% to 1%), AST/SGOT level raised, Hepatic necrosis
    (0.01% to 0.1%), Hepatotoxicity (chronic myeloid leukemia: all
    grades, 6% to 12%), Liver failure (0.01% to 0.1%)
    Neurologic: Cerebral edema, Raised intracranial pressure (0.01% to
    0.1%)
    Ophthalmic: Optic disc edema (0.01% to 0.1%)
    Otic: Sensorineural hearing loss
    Renal: Acute renal failure (0.1% to 1%)
    Respiratory: Acute respiratory failure, Hypoxia (Pediatrics, acute
    lymphoblastic leukemia, grade 3 or 4, 9%), Pleural effusion
    (Pediatrics, acute lymphoblastic leukemia, grade 3 or 4, 7%),
    Pneumonia (Chronic myeloid leukemia, 4% to 13%), Pneumonitis
    (Pediatric, acute lymphoblastic leukemia, grade 3 or 4, 8%)
    Other: Secondary malignant neoplastic disease, Tumor lysis
    syndrome
    Hysingla ER Common:
    Cardiovascular: Peripheral edema (1% to less than 5%%)
    Dermatologic: Pruritus (0% to less than 5%)
    Gastrointestinal: Abdominal pain (1% to less than 5%),
    Constipation (3% to 11%), Nausea (7% to 10%), Vomiting (3% to
    6%), Xerostomia (1% to less than 5%)
    Musculoskeletal: Spasm (1% to less than 5%)
    Neurologic: Dizziness (2% to 3%), Headache (2% to 4%),
    Somnolence (1% to 5%), Tremor (3%)
    Renal: Urinary tract infectious disease (1% to 5%)
    Respiratory: Upper respiratory infection (1% to 3%)
    Other: Fatigue (1% to 4%)
    Serious:
    Cardiovascular: Hypotension (less than 1%), Orthostatic
    hypotension (less than 1%), Prolonged QT interval, Syncope
    Gastrointestinal: Difficulty swallowing (less than 1%)
    Neurologic: Raised intracranial pressure, Seizure
    Respiratory: Respiratory depression
    Other: Drug withdrawal syndrome in neonate of dependent mother,
    Opioid withdrawal (less than 1%)
    Kuvan Common:
    Gastrointestinal: Diarrhea (4% or more), Vomiting (4% or more)
    Neurologic: Headache (4% or greater)
    Respiratory: Cough (4% or more), Nasal congestion (4% or more),
    Nasal discharge (4% or more), Pain in throat (4% or more), Upper
    respiratory infection (17%)
    Serious:
    Cardiovascular: Myocardial infarction
    Gastrointestinal: Gastrointestinal hemorrhage
    Hematologic: Hemorrhage, Post-procedural
    Neurologic: Seizure
    Respiratory: Respiratory failure
    Lamictal XR Common:
    Dermatologic: Rash (7% to 14%)
    Gastrointestinal: Abdominal pain (immediate-release, 5% to 10%),
    Diarrhea (immediate-release, 6% to 11%; extended-release, 5%),
    Indigestion (immediate-release, 2% to 7%), Nausea (immediate-
    release, 7% to 25%; extended-release, 7%), Vomiting (immediate-
    release, 5% to 20%; extended-release, 6%))
    Neurologic: Asthenia (immediate-release, 2% to 8%; extended-
    release, 6%), Ataxia (immediate-release, 2% to 11%), Coordination
    problem (immediate-release, 6% to 7%; extended-release, 3%),
    Dizziness (immediate-release, 7% to 54%; extended release, 14%),
    Headache (immediate-release, 29%), Insomnia (immediate-release,
    5% to 10%), Somnolence (immediate-release, 9% to 17%;
    extended-release, 5%), Tremor (immediate-release, 4% to 10%;
    extended-release, 6%), Vertigo (immediate-release, 2%; extended-
    release, 3%)
    Ophthalmic: Blurred vision (immediate-release, 11% to 25%
    (adults) and 4% (children); extended-release, 3%), Diplopia
    (immediate-release, 24% to 49% (adults) and 5% (children);
    extended-release, 5%)
    Psychiatric: Anxiety (immediate-release, 4%; extended-release,
    3%), Depression (immediate-release, 4%; extended-release, 3%)
    Reproductive: Dysmenorrhea (immediate-release, 5% to 7%)
    Respiratory: Rhinitis (immediate-release, 7% to 14%)
    Other: Pain (immediate-release, 5%)
    Serious:
    Dermatologic: Erythema multiforme (less than 0.1%), Rash,
    Serious (0.08% to 0.8%), Stevens-Johnson syndrome (0.08% to
    0.8%.), Toxic epidermal necrolysis (0.08% to 0.8%)
    Hematologic: Anemia (immediate release, less than 0.1%),
    Disseminated intravascular coagulation, Eosinophilia (immediate
    release, less than 0.1%), Leukopenia (immediate release, 0.1% to
    1%), Thrombocytopenia (immediate release, less than 0.1%)
    Hepatic: Liver failure
    Immunologic: Drug hypersensitivity syndrome
    Neurologic: Aseptic meningitis
    Other: Angioedema (less than 0.1%), Neuroleptic malignant
    syndrome
    Latuda Common:
    Gastrointestinal: Diarrhea (3% to 5%), Nausea (10% to 17%),
    Vomiting (2% to 8%)
    Neurologic: Akathisia (5.6% to 22%), Extrapyramidal disease
    (10% to 39%), Parkinsonism (5% to 17%), Somnolence (7.3% to
    26.5%)
    Psychiatric: Anxiety (4% to 5%)
    Serious:
    Cardiovascular: Orthostatic hypotension (0.3% to 2.1%), Syncope
    (0.1%)
    Hematologic: Agranulocytosis
    Neurologic: Cerebrovascular accident (0.1% to 1%), Seizure (less
    than 1%), Tardive dyskinesia, Transient ischemic attack
    Psychiatric: Suicidal thoughts (0.4% to 1.1%)
    Renal: Serum creatinine raised (2% to 4%)
    Other: Neuroleptic malignant syndrome
    Minastrin 24 FE Common:
    Dermatologic: Acne (2.7%)
    Endocrine metabolic: Abnormal weight gain (2%)
    Gastrointestinal: Nausea (4.6%), Vomiting (2% to 6%)
    Neurologic: Headache (6.3%)
    Psychiatric: Mood swings (2.2%)
    Reproductive: Abnormal cervical smear (3.1%), Amenorrhea (22%
    to 36%), Bacterial vaginosis (3.1%), Breast tenderness (3.4%),
    Candida vaginitis (6.1%), Intermenstrual bleeding - irregular (24 to
    35%), Menstrual cramp (4.4%)
    Serious:
    Cardiovascular: Myocardial infarction
    Hematologic: Arterial thrombosis, Venous thromboembolism
    Hepatic: Adenoma of liver, Liver carcinoma
    Neurologic: Cerebrovascular accident
    Ophthalmic: Thrombosis of retinal vein
    Nexavar Common:
    Cardiovascular: Hypertension, All grades (19.1%)
    Dermatologic: Acral erythema (hepatocellular carcinoma, 21%;
    renal cell carcinoma, 30%; thyroid carcinoma, 69%), Alopecia
    (hepatocellular carcinoma, 14%; renal cell carcinoma, 27%; thyroid
    carcinoma, 67%), Peeling of skin, Rash (up to 35%)
    Endocrine metabolic: Hypoalbuminemia (hepatocellular carcinoma,
    59%), Hypocalcemia (hepatocellular carcinoma, 27%; renal cell
    carcinoma, 12%; thyroid carcinoma, 36%), Hypophosphatemia
    (35% to 45%), Raised TSH level (thyroid carcinoma, 41%), Weight
    decreased (hepatocellular carcinoma, 30%; renal cell carcinoma,
    10%; thyroid carcinoma, 49%)
    Gastrointestinal: Abdominal pain (renal cell carcinoma, 11%;
    hepatocellular carcinoma, 31%; thyroid carcinoma, 20%), Decrease
    in appetite (thyroid carcinoma, 30%), Diarrhea (43% to 68%),
    Increased serum lipase level (40% to 41%), Loss of appetite (16%
    to 29%), Nausea (21% to 24%), Serum amylase raised (30% to
    34%)
    Hematologic: Lymphocytopenia (renal cell carcinoma, 23%;
    hepatocellular carcinoma, 47%), Thrombocytopenia (renal cell
    carcinoma; 12%; hepatocellular carcinoma, 46%)
    Hepatic: ALT/SGPT level raised, All grades (thyroid carcinoma,
    59%), AST/SGOT level raised, All grades (thyroid carcinoma,
    54%)
    Immunologic: Infectious disease (10% or greater)
    Other: Fatigue (37% to 46%), Pain (10% or greater)
    Serious:
    Cardiovascular: Congestive heart failure (1.9%), Hypertension,
    Grade 3 or 4 (4.3%), Hypertensive crisis (0.1% to less than 1%),
    Myocardial infarction, Myocardial ischemia, Prolonged QT interval
    (Less than 0.1%)
    Dermatologic: Squamous cell carcinoma of skin (thyroid
    carcinoma, 3%), Stevens-Johnson syndrome, Toxic epidermal
    necrolysis
    Gastrointestinal: Gastrointestinal hemorrhage, Gastrointestinal
    perforation (0.1% to less than 1%), Pancreatitis (0.1% to less than
    1%)
    Hematologic: Hemorrhage (renal cell carcinoma, 15.3%; thyroid
    carcinoma, 17.4%)
    Hepatic: ALT/SGPT level raised, Grade 3 or higher (thyroid
    carcinoma, 4%), AST/SGOT level raised, Grade 3 or 4 (thyroid
    carcinoma, 2%), Hepatitis (less than 0.1%)
    Neurologic: Cerebral hemorrhage (0.1% to less than 1%), Posterior
    reversible encephalopathy syndrome (0.1% to less than 1%)
    Respiratory: Interstitial lung disease (0.1% to less than 1%),
    Respiratory tract hemorrhage
    Noxafil Common:
    Endocrine metabolic: Hypokalemia (prophylaxis, 22% to 30%)
    Gastrointestinal: Diarrhea (prophylaxis, 29% to 42%;
    oropharyngeal candidiasis, 10%; refractory oropharyngeal
    candidiasis, 13%), Nausea (prophylaxis, 19% to 38%;
    oropharyngeal candidiasis, 9%; refractory oropharyngeal
    candidiasis, 29%), Vomiting (prophylaxis, 12% to 29%;
    oropharyngeal candidiasis, 7%; refractory oropharyngeal
    candidiasis, 28%)
    Neurologic: Headache (prophylaxis, 14% to 28%; oropharyngeal
    candidiasis, 8%; refractory oropharyngeal candidiasis, 20%)
    Other: Fever (prophylaxis, 21% to 45%; oropharyngeal candidiasis,
    6%; refractory oropharyngeal candidiasis, 34%)
    Serious:
    Cardiovascular: Prolonged QT interval (1% to 2%), Torsades de
    pointes (less than 5%)
    Hepatic: Cholestasis (rare), Liver failure (rare)
    Pradaxa Common:
    Gastrointestinal: Esophagitis, Gastritis, Gastroesophageal reflux
    disease (Atrial fibrillation, 5.5%), Gastrointestinal hemorrhage
    (DVT and pulmonary embolism, 0.7% to 3.1%; nonvalvular atrial
    fibrillation, 6.1%), Gastrointestinal ulcer, Indigestion (DVT and
    pulmonary embolism, 7.5%)
    Hematologic: Bleeding (DVT and pulmonary embolism
    prophylaxis, 10.5%; nonvalvular atrial fibrillation, 16.6%)
    Serious:
    Cardiovascular: Myocardial infarction (DVT and pulmonary
    embolism, 0.32% to 0.66%; nonvalvular atrial fibrillation, 0.7%)
    Gastrointestinal: Gastrointestinal hemorrhage, Major (DVT and
    pulmonary embolism, 0.3% to 0.6%; nonvalvular atrial fibrillation,
    1.6%)
    Hematologic: Bleeding, Major (DVT and pulmonary embolism,
    0.3% to 1.4%; nonvalvular atrial fibrillation, 3.3%), Thrombosis
    Immunologic: Anaphylaxis
    Neurologic: Epidural hematoma, Intracranial hemorrhage
    (nonvalvular atrial fibrillation, 0.3%; DVT and pulmonary
    embolism, 0.1%), Traumatic spinal subdural hematoma
    Respiratory: Bleeding, Alveolar
    Promacta Common:
    Gastrointestinal: Diarrhea (Chronic hepatitis C-associated
    thrombocytopenia, 19%; chronic idiopathic thrombocytopenic
    purpura, adults, 9%, pediatric, 5%; aplastic anemia, 21%), Nausea
    (Chronic hepatitis C-associated thrombocytopenia, 19%; chronic
    idiopathic thrombocytopenic purpura, 4% to 9%; aplastic anemia,
    33%), Pain in throat (Chronic idiopathic thrombocytopenic
    purpura, 4%; aplastic anemia, 14% 4%), Pharyngitis (4%),
    Vomiting (6%)
    Hematologic: Anemia (chronic hepatitis C-associated
    thrombocytopenia, 40%)
    Hepatic: ALT/SGPT level raised (Chronic idiopathic
    thrombocytopenic purpura, 5% to 6%; chronic ITP, pediatric, 6%),
    AST/SGOT level raised (Adult, 4%; pediatric, 5%),
    Hyperbilirubinemia (6% to 8%)
    Musculoskeletal: Myalgia (2% to 12%)
    Neurologic: Headache (Chronic hepatitis C-associated
    thrombocytopenia and aplastic anemia, 21%; chronic idiopathic
    thrombocytopenic purpura, 10%)
    Ophthalmic: Cataract (4% to 7%)
    Renal: Urinary tract infectious disease (5%)
    Respiratory: Cough (Aplastic anemia, 23%; chronic ITP, pediatric,
    9%), Epistaxis (13%)
    Other: Fatigue (Chronic hepatitis C-associated thrombocytopenia
    and aplastic anemia, 28%; chronic idiopathic thrombocytopenic
    purpura, 4%), Fever (Chronic hepatitis C-associated
    thrombocytopenia, 30%; aplastic anemia, 14%)
    Serious:
    Hematologic: Bleeding, Portal vein thrombosis (chronic hepatitis
    C-associated thrombocytopenia, 1%), Thrombosis (chronic
    hepatitis C-associated thrombocytopenia, 3%)
    Hepatic: Hepatotoxicity, Liver failure (chronic hepatitis C-
    associated thrombocytopenia, 7%), Liver function tests abnormal
    (11%)
    Renal: Acute renal failure
    Promacta
    Suboxone Common:
    Dermatologic: Hyperhidrosis (SL tablet, 14%; buccal film, 1% to
    less than 5%)
    Gastrointestinal: Abdominal pain (SL tablet, 11.2%), Constipation
    (SL tablet, 12.1%; buccal film, 1% to less than 5%), Nausea (SL
    tablet, induction phase, 5%; long-term use, 15%), Vomiting (SL
    tablet, 5% to 7.5%)
    Neurologic: Headache (SL tablet, induction phase, 7%; long-term
    use, 36.4%; buccal film, 5% or greater), Insomnia (SL tablet, 14%;
    buccal film, greater than 1% and less than 5%)
    Other: Drug withdrawal (SL tablet, 25.2%; buccal film, at least
    5%), Pain (SL tablet, 22.4%)
    Serious:
    Hepatic: Hepatitis
    Immunologic: Anaphylaxis
    Neurologic: Central nervous system depression
    Respiratory: Respiratory depression
    Other: Drug dependence (Buccal film, 1% to less than 5%)
    Tekturna HCT Common:
    Endocrine metabolic: Hyperkalemia (0.8% to 36.9%),
    Hypokalemia (2.2%)
    Gastrointestinal: Diarrhea (1.6%)
    Neurologic: Dizziness (2.3%)
    Renal: Serum blood urea nitrogen raised (11.8%)
    Respiratory: Cough (1.3%)
    Serious:
    Cardiovascular: Hypotension
    Ophthalmic: Angle-closure glaucoma, acute, Myopia (Acute),
    Transient
    Thalomid Common:
    Cardiovascular: Edema (multiple myeloma, 13% to 56%),
    Peripheral edema (erythema nodosum leprosum, 3.1% to 8.3%;
    multiple myeloma, 34%)
    Dermatologic: Dry skin (multiple myeloma, 21%), Rash (erythema
    nodosum leprosum, 20.8%)
    Endocrine metabolic: Hypocalcemia (multiple myeloma, 72%),
    Weight gain (multiple myeloma, 3% to 22%), Weight loss
    (multiple myeloma, 23%)
    Gastrointestinal: Constipation (erythema nodosum leprosum, 2.8%
    to 9.4%; multiple myeloma, 50% to 55%), Diarrhea (erythema
    nodosum leprosum, 4.2% to 18.7%), Indigestion (multiple
    myeloma, 11%), Nausea (erythema nodosum leprosum, 4.2%;
    multiple myeloma, 13% to 28%)
    Hematologic: Leukopenia (erythema nodosum, 16.7% to 25%;
    multiple myeloma, 35%)
    Musculoskeletal: Muscle weakness (multiple myeloma, 40%)
    Neurologic: Asthenia (erythema nodosum leprosum, 5.6% to
    21.9%; multiple myeloma, 24%), Confusional state (multiple
    myeloma, 28%), Dizziness (erythema nodosum leprosum, 4.2% to
    19.2%; multiple myeloma, 23%), Somnolence (erythema nodosum
    leprosum, 36.1% to 37.5%; multiple myeloma, 3% or more),
    Tremor (erythema nodosum leprosum, 4.2%; multiple myeloma,
    26%)
    Respiratory: Dyspnea (multiple myeloma, 42%), Pneumonia
    (multiple myeloma, 15%)
    Other: Fatigue (multiple myeloma, 21% to 79%), Fever (erythema
    nodosum leprosum, 19.4% to 21.9%; multiple myeloma, 24%)
    Serious:
    Cardiovascular: Atrial fibrillation, Grade 3/4 (multiple myeloma,
    5%), Cardiac dysrhythmia, Ischemic heart disease (11.1%),
    Myocardial infarction (1.3%)
    Tikosyn Common:
    Cardiovascular: Chest pain (10%)
    Neurologic: Dizziness (8%), Headache (11%)
    Serious:
    Cardiovascular: Heart block (up to 1.2%), Prolonged QT interval,
    Torsades de pointes (0.8%), Ventricular arrhythmia (up to 14.5%),
    Ventricular fibrillation (up to 4.8%), Ventricular tachycardia (up to
    12.4%)
    Tradjenta Common:
    Endocrine metabolic: Hypoglycemia (monotherapy, 6.6%;
    combination therapy, 22.9%)
    Respiratory: Nasopharyngitis (7%)
    Serious:
    Gastrointestinal: Pancreatic cancer, Pancreatitis
    Immunologic: Anaphylaxis, Hypersensitivity reaction
    Other: Angioedema, Pancreatic cancer
    Trokendi XR Common:
    Dermatologic: Flushing (pediatrics, 5%)
    Endocrine metabolic: Serum bicarbonate level abnormal (25% to
    67%)
    Gastrointestinal: Loss of appetite (10% to 24%), Weight decreased
    (4% to 21%)
    Immunologic: Infectious disease (2% to 8%)
    Neurologic: Confusion (3% to 11%), Dizziness (4% to 25%),
    Impaired cognition (2% to 7%), Impaired psychomotor
    performance (2% to 13%), Memory impairment (3% to 12%),
    Paresthesia (1% to 51%), Reduced concentration span (2% to
    10%), Somnolence (6% to 29%)
    Psychiatric: Feeling nervous (4% to 16%), Mood disorder (4% to
    11%)
    Other: Fatigue (6% to 16%), Fever (1% to 12%)
    Serious:
    Dermatologic: Erythema multiforme, Stevens-Johnson syndrome,
    Toxic epidermal necrolysis
    Endocrine metabolic: Hyperammonemia (Adolescents, 26%),
    Hypohidrosis, Increased body temperature, Metabolic acidosis
    Hepatic: Liver failure
    Neurologic: Drug-induced encephalopathy
    Ophthalmic: Glaucoma, Myopia, Visual field defect (epilepsy,
    0.1% to 1%)
    Psychiatric: Suicidal thoughts
    Renal: Nephrolithiasis (adults, 1% to 3%)
    Viibryd Common:
    Gastrointestinal: Diarrhea (26% to 29%), Nausea (22% to 24%),
    Vomiting (4% to 5%)
    Neurologic: Insomnia (6% to 7%)
    Serious:
    Cardiovascular: Ventricular premature beats (0.1% to 1%)
    Psychiatric: Suicidal behavior, Suicidal thoughts
    Other: Drug withdrawal, Serotonin syndrome (0.1%)
    Xartemis XR Common:
    Gastrointestinal: Constipation (extended-release, 4%), Nausea
    (extended-release, 31%), Vomiting (extended-release, 9%)
    Neurologic: Dizziness (extended-release, 13%), Headache
    (extended-release, 10%), Lightheadedness, Sedated, Somnolence
    (extended-release, 4%)
    Serious:
    Cardiovascular: Disorder of pulmonary circulation, Hypotension,
    Shock
    Dermatologic: Acute generalized exanthematous pustulosis,
    Stevens-Johnson syndrome, Toxic epidermal necrolysis
    Hematologic: Agranulocytosis, Neutropenia
    Hepatic: Hepatic necrosis, Hepatotoxicity, Liver failure
    Immunologic: Anaphylaxis, Hypersensitivity reaction
    Respiratory: Apnea, Respiratory arrest, Respiratory depression
    Other: Neonatal Abstinence Syndrome
    Zohydro ER Common:
    Cardiovascular: Peripheral edema (1% to less than 5%%)
    Dermatologic: Pruritus (0% to less than 5%)
    Gastrointestinal: Abdominal pain (1% to less than 5%),
    Constipation (3% to 11%), Nausea (7% to 10%), Vomiting (3% to
    6%), Xerostomia (1% to less than 5%)
    Musculoskeletal: Spasm (1% to less than 5%)
    Neurologic: Dizziness (2% to 3%), Headache (2% to 4%),
    Somnolence (1% to 5%), Tremor (3%)
    Renal: Urinary tract infectious disease (1% to 5%)
    Respiratory: Upper respiratory infection (1% to 3%)
    Other: Fatigue (1% to 4%)
    Serious:
    Cardiovascular: Hypotension (less than 1%), Orthostatic
    hypotension (less than 1%), Prolonged QT interval, Syncope
    Gastrointestinal: Difficulty swallowing (less than 1%)
    Neurologic: Raised intracranial pressure, Seizure
    Respiratory: Respiratory depression
    Other: Drug withdrawal syndrome in neonate of dependent mother,
    Opioid withdrawal (less than 1%)
    Zorvolex Common
    Gastrointestinal: Constipation (5% to 8%), Diarrhea (6%), Nausea
    (6% to 7%)
    Hepatic: Increased liver function test (15%)
    Neurologic: Headache (4% to 8%)
    Renal: Urinary tract infectious disease (7%)
    Respiratory: Nasopharyngitis (6%), Sinusitis (3% to 5%), Upper
    respiratory infection (8%)
    Serious
    Cardiovascular: Myocardial infarction, Thrombosis
    Dermatologic: Erythema multiforme, Erythroderma, Stevens-
    Johnson syndrome, Toxic epidermal necrolysis
    Gastrointestinal: Gastrointestinal hemorrhage, Gastrointestinal
    perforation
    Hematologic: Aplastic anemia, Blood coagulation disorder,
    Hemolytic anemia, Thrombocytopenia
    Hepatic: Increased liver enzymes, Jaundice, Liver failure
    Immunologic: Anaphylactoid reaction
    Neurologic: Cerebrovascular accident
    Renal: Acute renal failure
    Respiratory: Bronchospasm
    Zytiga Common
    Dermatologic: Contusion (13.3%), Flushing (19% to 22.3%)
    Endocrine metabolic: Hypercholesterolemia (Greater than 20%),
    Hyperglycemia (56.6%), Hypertriglyceridemia (62.5%),
    Hypophosphatemia (23.8%)
    Gastrointestinal: Diarrhea (17.6% to 21.6%), Vomiting (10% or
    higher)
    Hematologic: Anemia (Greater than 20%), Lymphocytopenia, All
    grades (38.2%)
    Hepatic: Alkaline phosphatase raised (Greater than 20%)
    Musculoskeletal: Joint swelling (29.5% to 30.3%)
    Renal: Urinary tract infectious disease (11.5%)
    Respiratory: Cough (10.6% to 17.3%), Dyspnea (11.8%)
    Other: Fatigue (39.1%)
    Serious
    Cardiovascular: Cardiac dysrhythmia (7.2%), Cardiorespiratory
    arrest (0.5%), Chest discomfort, Chest pain, Edema (25.1% to
    26.7%), Heart failure (2.1% to 2.3%), Hypertension (8.5% to
    21.6%), Myocardial infarction, Sudden cardiac death
    Endocrine metabolic: Adrenal insufficiency (0.5%), Hypokalemia
    (17.2% to 28.3%)
    Hematologic: Lymphocytopenia, Grade 3 or 4 (8.7%)
    Hepatic: ALT/SGPT level raised (11.1% to 41.9%), AST/SGOT
    level raised (30.6% to 37.3%), Serum bilirubin raised (6.6%)
    Seroquel (Quetiapine) Common:
    Cardiovascular: Increased diastolic arterial pressure (Pediatric,
    40.6%), Increased systolic arterial pressure (Pediatric, 15.2%),
    Orthostatic hypotension (Up to 7%), Tachycardia (Up to 6%)
    Endocrine metabolic: Serum cholesterol raised (7% to 18%), Serum
    triglycerides raised (8% to 28%), Weight gain (3% to 28%)
    Gastrointestinal: Abdominal pain (3% to 7%), Constipation (2% to
    11%), Increased appetite (2% to 12%), Indigestion (2% to 7%),
    Nausea (Pediatric, 6% to 10%), Vomiting (Pediatric, 7% to 8%),
    Xerostomia (Adult, 9% to 44%; pediatric, 4% to 10%)
    Hepatic: Increased liver enzymes (1% to 6%)
    Musculoskeletal: Backache (3% to 5%)
    Neurologic: Asthenia (Up to 10%), Dizziness (8% to 19%),
    Extrapyramidal disease (1.1% to 12.9%), Headache (17% to 21%),
    Insomnia (8% to 12%), Lethargy (1% to 5%), Somnolence (18% to
    57%), Tremor (2% to 8%)
    Psychiatric: Agitation (6% to 20%)
    Respiratory: Nasal congestion (3% to 5%), Pharyngitis (4% to 6%)
    Other: Fatigue (3% to 14%), Pain (7%)
    Serious:
    Cardiovascular: Prolonged QT interval (0.1% to less than 1%),
    Sudden cardiac death, Syncope (0.3% to 1%)
    Endocrine metabolic: Diabetic ketoacidosis
    Gastrointestinal: Pancreatitis
    Hematologic: Agranulocytosis, Leukopenia, Neutropenia (0.3% to
    1.5%)
    Immunologic: Anaphylaxis
    Neurologic: Seizure (0.05% to 0.5%), Tardive dyskinesia
    Psychiatric: Suicidal thoughts
    Reproductive: Priapism
    Other: Neuroleptic malignant syndrome
    Pain Relievers
    Opioids
    Codeine Common
    Gastrointestinal: Constipation, Nausea, Vomiting
    Neurologic: Dizziness, Lightheadedness, Sedated, Somnolence
    Respiratory: Dyspnea
    Serious
    Cardiovascular: Hypotension
    Gastrointestinal: Bowel obstruction, Pancreatitis
    Neurologic: CSF pressure: raised, Seizure
    Respiratory: Respiratory depression
    Fentanyl and Analogs Common
    Cardiovascular: Hypotension (up to 5% (buccal film)), Peripheral
    edema (1% or greater (nasal spray); 5% to 32% (buccal tablet))
    Dermatologic: Application site reaction (10% (buccal tablet)), Rash
    (3% to 8% (lozenge))
    Endocrine metabolic: Abnormal weight loss (up to 13% (buccal
    tablet/film)), Hypokalemia (up to 15% (buccal tablet))
    Gastrointestinal: Abdominal pain (1% or greater (nasal spray); up
    to 15%), Constipation (4% to 26%), Diarrhea (up to 16% (buccal
    tablet/film)), Loss of appetite (2% to 11% (buccal tablet/film)),
    Nausea (5.6% to 42%), Vomiting (4% to 37%)
    Hematologic: Anemia (1% or greater (nasal spray); 9% to 32%
    (buccal tablet)), Neutropenia (1% or greater (nasal spray); up to 8%
    (buccal tablet))
    Musculoskeletal: Arthralgia (up to 8% (buccal tablet)), Backache
    (up to 11% (buccal tablet))
    Neurologic: Asthenia (up to 30% (lozenge, buccal tablet/film)),
    Confusion (up to 16%), Dizziness (6% (nasal spray); up to 26%
    (lozenge, sublingual, buccal tablet/film)), Headache (1% or greater
    (nasal spray); up to 17% (lozenge, sublingual, buccal tablet/film)),
    Insomnia (up to 11% (lozenge, buccal tablet/film)), Somnolence
    (up to 15% (sublingual, buccal tablet))
    Psychiatric: Anxiety (3% to 9% (buccal film, lozenge)), Depression
    (up to 11% (buccal tablet))
    Respiratory: Cough (up to 9%), Pneumonia (1% to 16% (buccal
    tablet, nasal spray))
    Other: Dehydration (up to 21% (buccal tablet, film)), Fatigue (1%
    to 20% (buccal tablet, film))
    Serious
    Cardiovascular: Bradyarrhythmia (1% or greater (sublingual
    tablet)), Cardiorespiratory arrest (1% or greater (nasal spray)),
    Tachyarrhythmia (1% or greater (sublingual, buccal tablet/film))
    Gastrointestinal: Bowel obstruction (1% or greater (buccal film); up
    to 4% (lozenge))
    Hematologic: Deep venous thrombosis (1% or greater (nasal
    spray))
    Musculoskeletal: Muscle rigidity
    Respiratory: Dyspnea (up to 19% (lozenge, buccal tablet/film)),
    Respiratory depression
    (Causing Overdoses)
    Hydrocodone Common
    Cardiovascular: Peripheral edema (1% to less than 5%%)
    Dermatologic: Pruritus (0% to less than 5%)
    Gastrointestinal: Abdominal pain (1% to less than 5%),
    Constipation (3% to 11%), Nausea (7% to 10%), Vomiting (3% to
    6%), Xerostomia (1% to less than 5%)
    Musculoskeletal: Spasm (1% to less than 5%)
    Neurologic: Dizziness (2% to 3%), Headache (2% to 4%),
    Somnolence (1% to 5%), Tremor (3%)
    Renal: Urinary tract infectious disease (1% to 5%)
    Respiratory: Upper respiratory infection (1% to 3%)
    Other: Fatigue (1% to 4%)
    Serious
    Cardiovascular: Hypotension (less than 1%), Orthostatic
    hypotension (less than 1%), Prolonged QT interval, Syncope
    Gastrointestinal: Difficulty swallowing (less than 1%)
    Neurologic: Raised intracranial pressure, Seizure
    Respiratory: Respiratory depression
    Other: Drug withdrawal syndrome in neonate of dependent mother,
    Opioid withdrawal (less than 1%)
    Hydromorphone Common
    Dermatologic: Flushing (extended-release, less than 2%), Pruritus
    (extended-release, 1% to 8%), Sweating
    Gastrointestinal: Constipation (extended-release, 7% to 31%),
    Nausea (extended-release, 9% to 28%.), Vomiting (extended-
    release, 6% to 14%)
    Neurologic: Asthenia (1% to 11%), Dizziness (1% to 11%),
    Headache (1% to 12%), Somnolence (less than 2%)
    Serious
    Cardiovascular: Hypotension (less than 2%), Syncope (less than
    2%)
    Neurologic: Coma, Myoclonus (less than 2%), Raised intracranial
    pressure, Seizure (less than 2%)
    Psychiatric: Suicidal thoughts (extended-release, less than 2%)
    Respiratory: Apnea (less than 1%), Respiratory arrest, Respiratory
    depression (less than 2%)
    Other: Drug dependence (less than 1%), Drug withdrawal (less than
    1%), Neonatal Abstinence Syndrome
    Methadone Common
    Cardiovascular: Hypotension
    Endocrine metabolic: Diaphoresis
    Gastrointestinal: Constipation, Nausea, Vomiting
    Neurologic: Asthenia, Dizziness, Lightheadedness, Sedated
    Serious
    Cardiovascular: Decreased vascular flow, left ventricle, Prolonged
    QT interval, Torsades de pointes
    Endocrine metabolic: Hypoglycemia
    Respiratory: Respiratory acidosis, Respiratory arrest, Respiratory
    depression
    Other: Drug dependence
    Oxycodone Common
    Dermatologic: Pruritus (Adults, controlled-release, 13%;
    immediate-release, 3% or greater; pediatrics, 6%), Sweating
    (controlled-release, 5%; immediate-release, less than 3%)
    Gastrointestinal: Abdominal pain (up to 5%), Constipation (Adults,
    controlled-release, 23%; immediate-release, 3% or greater;
    pediatrics, 9%), Nausea (Adults, controlled-release, 23%;
    immediate-release, 3% or greater; pediatrics, 15%), Vomiting
    (Adults, controlled-release, 12%; immediate-release, 3% or greater;
    pediatrics, 21%), Xerostomia (controlled-release, 6%; immediate-
    release, less than 3%)
    Neurologic: Asthenia (controlled-release, 6%; immediate-release,
    3% or greater), Dizziness (Adults, controlled-release, 13%;
    immediate-release, 3% or greater; pediatrics, 9%), Headache
    (Adults, 3% or greater; pediatrics, 14%), Somnolence (controlled-
    release, 23%; immediate-release, 3% or greater)
    Other: Fever (Adults, up to 5%; pediatrics, 11%)
    Serious
    Cardiovascular: Cardiac arrest, Chest pain (less than 1%), Heart
    failure (less than 3%), Hypotension (less than 3%), Shock, ST
    segment depression (less than 1%), Syncope (less than 1%)
    Gastrointestinal: Bowel obstruction, Diverticulitis, Exacerbation
    Immunologic: Hypersensitivity reaction (less than 3%)
    Respiratory: Respiratory depression
    Other: Drug withdrawal syndrome in neonate of dependent mother,
    Opioid withdrawal (1% to 5%)
    Oxymorphone Common
    Cardiovascular: Hypotension (less than 10%)
    Dermatologic: Pruritus (less than or equal to 15.2%), Sweating
    symptom (1% to less than 10%)
    Gastrointestinal: Abdominal pain (1% to less than 10%),
    Constipation (4.1% to 27.6%), Nausea (2.9% to 33.1%), Vomiting
    (less than or equal to 15.6%), Xerostomia (1% to less than 10%)
    Neurologic: Confusion (1% to less than 10%), Dizziness (5% to
    17%), Headache (4% to 12%), Somnolence (2% to 19%)
    Respiratory: Dyspnea (1% to less than 10%), Hypoxia (less than
    10%)
    Other: Fatigue (1% to less than 10%), Fever (1% to 14.2%)
    Serious
    Gastrointestinal: Bowel obstruction (less than 1%)
    Neurologic: Coma
    Respiratory: Respiratory depression
    Other: Drug dependence, Drug withdrawal syndrome in neonate of
    dependent mother
    Amytal (amobarbital) Common
    Neurologic: Confusion, Dizziness, Headache, Somnolence
    Serious
    Dermatologic: Stevens-Johnson syndrome (rare)
    Hematologic: Agranulocytosis (rare), Megaloblastic anemia, With
    prolonged use (rare)
    Hepatic: Injury of liver, With prolonged use (rare)
    Respiratory: Apnea, Hypoventilation
    Nembutal (pentobarbital) Common
    Neurologic: Confusion (less than 1%), Dizziness (less than 1%),
    Somnolence (1% to 3%)
    Psychiatric: Agitation (less than 1%)
    Serious
    Dermatologic: Stevens-Johnson syndrome (less than 1%)
    Hematologic: Megaloblastic anemia (less than 1%)
    Hepatic: Injury of liver (less than 1%)
    Respiratory: Apnea (less than 1%), Hypoventilation (less than 1%)
    Seconal (secobarbital) Common
    Neurologic: Somnolence (1% to 3%)
    Serious
    Hematologic: Megaloblastic anemia, With prolonged use (less than
    1%)
    Hepatic: Liver damage (less than 1%)
    Psychiatric: Complex mannerisms - behavior (Less than 1%.)
    Other: Drug dependence, Withdrawal sign or symptom
    Adderall (Amphetamine) Common
    Cardiovascular: Increased systolic arterial pressure (extended-
    release: pediatrics, 7% to 35%)
    Endocrine metabolic: Weight loss (extended-release: adults, 10%;
    pediatrics, 4% to 9%)
    Gastrointestinal: Abdominal pain (extended-release: pediatrics,
    11% to 14%), Loss of appetite (extended-release capsules: adults,
    33%; pediatrics, 22% to 36%), Xerostomia (extended-release:
    adults, 35%; pediatrics, 2% to 4%)
    Neurologic: Dizziness, Headache (extended-release: adults, 26%),
    Insomnia (extended-release: adults, 27%; pediatrics, 12% to 17%)
    Psychiatric: Feeling nervous (extended release: adults, 13%;
    pediatrics, 6%)
    Serious
    Cardiovascular: Cardiomyopathy, Myocardial infarction, Peripheral
    vascular disease, Raynaud's disease, Sudden cardiac death
    Dermatologic: Stevens-Johnson syndrome, Toxic epidermal
    necrolysis
    Immunologic: Hypersensitivity reaction
    Neurologic: Cerebrovascular accident, Seizure
    Psychiatric: Psychotic disorder
    Methylphenidate Common
    Cardiovascular: Tachycardia (Adult, 4.8%)
    Dermatologic: Diaphoresis (Adult, 5.1%)
    Endocrine metabolic: Weight decreased (Adult, 6.5%)
    Gastrointestinal: Abdominal pain (2% or greater), Decrease in
    appetite (Adult, 25.3%; pediatric, 2% to 9% or greater), Loss of
    appetite (Adult, 1.7%; pediatric, 3.1% to 9% or greater), Nausea
    (Adult, 12.8%), Vomiting (2% or greater), Xerostomia (Adult,
    14%)
    Neurologic: Dizziness (Adult, 6.7%; pediatric, 1.9%.), Headache
    (Adult, 22.2%; pediatric, up to 12%), Insomnia (Adult, 12.3%;
    pediatric, 2.8% to 5%)
    Psychiatric: Anxiety (Adult, 8.2%), Depression (Adult, 1.7% to
    3.9%), Irritability (Adult, 5.8%)
    Serious
    Cardiovascular: Myocardial infarction, Raynaud's phenomenon,
    Sudden cardiac death
    Endocrine metabolic: Decreased body growth
    Gastrointestinal: Gastrointestinal obstruction, With preexisting
    severe gastrointestinal narrowing and use of controlled-release
    formulations
    Hepatic: Abnormal liver function
    Neurologic: Cerebral artery occlusion, Cerebral hemorrhage,
    Cerebrovascular accident, Seizure
    Ophthalmic: Blurred vision (1.7% to 2% or greater)
    Psychiatric: Aggressive behavior (Adult, 1.7%), Mania, Psychotic
    disorder
    Reproductive: Priapism
    Daytrana See Methylphenidate
    Concerta See Methylphenidate
    Ritalin See Methylphenidate
    Klonopin (clonazepam) Common
    Neurologic: Ataxia (5% to 30%), Coordination problem (6%),
    Dizziness (8%), Somnolence (37% to 50%)
    Psychiatric: Problem behavior (25%)
    Respiratory: Upper respiratory infection (8%)
    Other: Fatigue (7%)
    Serious
    Psychiatric: Depression (7%), Suicidal thoughts
    Respiratory: Respiratory depression
    Valium (diazepam) Common
    Cardiovascular: Hypotension
    Dermatologic: Rash (3%, rectal gel)
    Gastrointestinal: Diarrhea (4%, rectal gel)
    Musculoskeletal: Muscle weakness
    Neurologic: Ataxia, Incoordination (3%, rectal gel), Somnolence
    Psychiatric: Euphoria (3%, rectal gel)
    Respiratory: Respiratory depression
    Other: Fatigue
    Serious
    Hematologic: Neutropenia
    Xanax (alprazolam) Common
    Endocrine metabolic: Decrease in appetite (7.3% to 27.8%),
    Increased appetite (7% to 32.7%), Weight increase (2.7% to 27.2%)
    Gastrointestinal: Constipation (8.1% to 26.2%), Reduced salivation
    (32.8%), Xerostomia (10.2% to 14.7%)
    Neurologic: Cognitive disorder (28.8%), Confusion (1.5% to
    10.4%), Dysarthria (10.9% to 23.3%), Incoordination (9.4% to
    40.1%), Lightheadedness (20.8%), Memory impairment (15.4% to
    33.1%), Sedated (45.2%), Somnolence (23% to 76.8%)
    Psychiatric: Irritability (immediate-release, 33.1%; extended-
    release 1% or more)
    Reproductive: Reduced libido (6% to 14.4%)
    Other: Fatigue (13.9% to 48.6%)
    Serious
    Dermatologic: Stevens-Johnson syndrome
    Ambien (zolpidem) Common
    Gastrointestinal: Diarrhea (1% to 3%), Nausea (1% to 7%)
    Immunologic: Allergic reaction (4%)
    Neurologic: Dizziness (1% to 23.5%), Drugged state (3%),
    Headache (1% to 19%), Somnolence (2% to 15%)
    Ophthalmic: Visual disturbance (3%)
    Other: Fatigue (0.1% to 3%)
    Serious
    Cardiovascular: Chest pain (1%), Tachycardia (0.1% to 1%)
    Immunologic: Anaphylaxis (rare)
    Neurologic: Hepatic encephalopathy
    Psychiatric: Complex mannerisms - behavior, Depression,
    worsening, Suicidal thoughts
    Other: Angioedema (rare)
    Lunesta (eszopiclone) Common
    Gastrointestinal: Disorder of taste (8% to 34%), Vomiting (3%)
    Neurologic: Dizziness (1% to 7%), Headache (13% to 21%),
    Migraine (1% or greater)
    Respiratory: Respiratory tract infection (5% to 10%)
    Serious
    Other: Angioedema (rare)
    Sonata (zaleplon) Common
    Neurologic: Dizziness (7% to 9%), Headache (30% to 42%)
    Serious
    Immunologic: Anaphylaxis (rare)
    Neurologic: Drug withdrawal seizure (rare)
    Psychiatric: Abnormal behavior, Complex mannerisms - behavior,
    Depression (at least 1%), Suicidal behavior, Suicidal thoughts
    Other: Angioedema (rare)
    Chantix Common
    Gastrointestinal: Constipation (5% to 8%), Flatulence (6% to 9%),
    Nausea (30%), Vomiting (5% to 11%)
    Neurologic: Dream disorder (9% to 13%), Headache (11% to 19%),
    Insomnia (10% to 19%)
    Serious
    Cardiovascular: Angina (2.3%), Myocardial infarction (2%)
    Neurologic: Cerebrovascular accident
    Ophthalmic: Acquired night blindness (rare), Blurred vision
    (infrequent), Retinal vascular disorder (rare), Subcapsular cataract
    (rare), Transient blindness (rare), Visual disturbance (infrequent)
    Psychiatric: Abnormal behavior, Depression (3.5% to 11%),
    Hostile behavior (2%), Mood disorder (2.3%), Suicidal behavior,
    and/or ideation (6% to 11%)
    Revlimid Common
    Cardiovascular: Peripheral edema (multiple myeloma, 26.3%;
    myelodysplastic syndrome, 20.3%; mantle cell lymphoma, 16%)
    Dermatologic: Pruritus (Multiple myeloma, 7.6%; myelodysplastic
    syndrome, 41.9%; mantle cell lymphoma, 17%), Rash (Multiple
    myeloma, up to 26.1%; myelodysplastic syndrome, 35.8%; mantle
    cell lymphoma, 22%)
    Endocrine metabolic: Hypokalemia (Multiple myeloma, 13.6% to
    17.1%; myelodysplastic syndrome, 10.8%; mantle cell lymphoma,
    13%), Weight decreased (13% to 19.5%)
    Gastrointestinal: Constipation (Multiple myeloma, 40.5%;
    myelodysplastic syndrome, 23.6%; mantle cell lymphoma, 16%),
    Diarrhea (Multiple myeloma, 38.5% to 45.5%; myelodysplastic
    syndrome, 48.6%; mantle cell lymphoma, 31%), Nausea (23.6% to
    30%')
    Hematologic: Anemia, All grades (Multiple myeloma, 31.4% to
    43.8%; myelodysplastic syndrome, 11.5%; mantle cell lymphoma,
    31%), Leukopenia, All grades (7.9% to 15%), Neutropenia, All
    grades (Multiple myeloma, 35% to 42.2%; myelodysplastic
    syndrome, 58.8%; mantle cell lymphoma, 49%),
    Thrombocytopenia, All grades (Multiple myeloma, 19.5% to
    21.5%; myelodysplastic syndrome, 61.5%; mantle cell lymphoma,
    36%)
    Musculoskeletal: Arthralgia (Multiple myeloma, 19%;
    myelodysplastic syndrome, 21.6%; mantle cell lymphoma, 8%),
    Backache (Multiple myeloma, 25.8% to 32%; myelodysplastic
    syndrome, 20.9%; mantle cell lymphoma, 13%), Cramp (Multiple
    myeloma, 33.4%; myelodysplastic syndrome, 18.2%)
    Neurologic: Asthenia (Multiple myeloma, 28.2%; myelodysplastic
    syndrome, 14.9%; mantle cell lymphoma, 14%), Dizziness (19.6%
    to 23.2%), Headache (Myelodysplastic syndrome, 19.6%),
    Insomnia (Multiple myeloma, 27.6%; myelodysplastic syndrome,
    10.1%), Tremor (Multiple myeloma, 21.2%)
    Ophthalmic: Blurred vision (Multiple myeloma, 17.3%)
    Respiratory: Cough (Multiple myeloma, 22.7%; myelodysplastic
    syndrome, 19.6%; mantle cell lymphoma, 28%), Dyspnea (Multiple
    myeloma, 22% to 23.5%; myelodysplastic syndrome, 6.8% to
    16.9%; mantle cell lymphoma, 18%), Epistaxis (Myelodysplastic
    syndrome, 14.9%), Nasopharyngitis (Multiple myeloma, 15% to
    17.6%; myelodysplastic syndrome, 23%), Pharyngitis (13.6% to
    15.5%), Upper respiratory infection (Multiple myeloma, 24.6%;
    myelodysplastic syndrome, 14.9%; mantle cell lymphoma, 13%)
    Other: Fatigue (Multiple myeloma, 32.5% to 43.9%;
    myelodysplastic syndrome, 31.1%; mantle cell lymphoma, 34%),
    Fever (Multiple myeloma, 21.4% to 27.5%; myelodysplastic
    syndrome, 20.9%; mantle cell lymphoma, 23%), Infectious disease
    Serious
    Cardiovascular: Atrial fibrillation, Grade 3 or 4 (multiple myeloma,
    3.7%), Cerebrovascular accident (1.4% to 2.3%), Congestive heart
    failure, Grade 3 or 4 (multiple myeloma, 1.4%), Myocardial
    infarction (Less than 5%), Syncope, Grade 3 or 4 (1.4% to 2.8%)
    Dermatologic: Stevens-Johnson syndrome, Toxic epidermal
    necrolysis
    Hematologic: Anemia, Grade 3 or 4 (Multiple myeloma, 9.9% to
    18.2%; myelodysplastic syndrome, 6.1%; mantle cell lymphoma,
    11%), Deep venous thrombosis, All grades (9.3% to 10.3%), Deep
    venous thrombosis, Grade 3 or 4 (4% to 8.2%), Febrile neutropenia,
    Grade 3 or 4 (2.3% to 6%), Leukopenia, Grade 3 or 4 (4% to 7%),
    Neutropenia, Grade 3 or 4 (Multiple myeloma, 16% to 33.4%
    myelodysplastic syndrome, 53.4%; mantle cell lymphoma, 43%.),
    Thrombocytopenia, Grade 3 or 4 (Multiple myeloma, 8.3% to
    12.2%; myelodysplastic syndrome, 50%; mantle cell lymphoma,
    28%), Thrombosis
    Hepatic: Hepatotoxicity (15%), Liver failure
    Ophthalmic: Cataract, Grade 3 or 4 (Multiple myeloma, 9.6%;
    1.4% (grade 3.4))
    Renal: Interstitial nephritis, acute
    Respiratory: Hypoxia (Mantle cell lymphoma, 2%), Pleural
    effusion (Mantle cell lymphoma, 7%), Pneumonia (Multiple
    myeloma, 13.6% to 17.5%; myelodysplastic syndrome, 11.5%;
    mantle cell lymphoma, 14%), Pneumonitis (Myelodysplastic
    syndrome, grade 3 or 4, 1.4%), Pulmonary embolism, Grade 3 or 4
    (2% to 4%), Pulmonary hypertension (Myelodysplastic syndrome,
    grade 3 or 4, 1.4%), Respiratory distress (Grade 3 or 4, 1% to 2%)
    Other: Angioedema, Multiple organ failure (Myelodysplastic
    syndrome, grade 3 or 4, 1.4%), Secondary malignant neoplastic
    disease, Tumor flare (Mantle cell lymphoma, 10%), Tumor lysis
    syndrome
    Tracleer Common
    Cardiovascular: Edema of lower extremity (5% to 8%),
    Hypotension (7%), Palpitations (5%)
    Dermatologic: Flushing (7% to 14%)
    Hematologic: Decreased hemoglobin (6%)
    Neurologic: Headache (up to 24%)
    Serious
    Hematologic: Decreased hemoglobin (Severe) (3%)
    Hepatic: Cirrhosis of liver, Increased liver aminotransferase level
    (Up to 11%), Liver failure
    Other: Angioedema
    Xeljanz (Jak Compounds) Common
    Endocrine metabolic: Increased HDL level (10% to 12%), Raised
    low density lipoprotein cholesterol (15% to 19%)
    Neurologic: Headache (3.4% to 4.3%)
    Renal: Urinary tract infectious disease (2%)
    Respiratory: Nasopharyngitis (2.8% to 3.8%), Upper respiratory
    infection (3.8% to 4.5%)
    Serious
    Dermatologic: Skin cancer, Non-melanoma
    Gastrointestinal: Gastrointestinal perforation
    Hematologic: Anemia, Decreased lymphocyte count (0.04%),
    Neutropenia (0.07%)
    Hepatic: Injury of liver
    Immunologic: Infectious disease (20% to 22%), Opportunistic
    infection, Post-transplant lymphoproliferative disorder, Epstein
    Barr virus associated (2.3%), Tuberculosis
    Other: Cancer
    Atomoxetine (Strattera) Common
    Cardiovascular: Increased diastolic arterial pressure (adult, 4.8% to
    12.6%; pediatric, 9.3% to 21.5%), Increased systolic arterial
    pressure (adult, 4.2% to 12.4%; pediatric, 4.9% to 12.5%),
    Tachycardia (adult, 1.5% to 22.4%; pediatric, 0.3% to 23.4%)
    Endocrine metabolic: Weight decreased (adults, 2%; pediatric, 3%
    to 29.1%)
    Gastrointestinal: Abdominal pain (adult, 7%; pediatric, 17% to
    18%), Constipation (adult, 8%; pediatric, 1% to 2%), Decrease in
    appetite (adult, 16%; pediatric, 16%), Nausea (adult, 26%;
    pediatric, 7% to 13%), Vomiting (adult, 4%; pediatric, 11%),
    Xerostomia (adult, 20%)
    Neurologic: Headache (pediatric, 19%), Insomnia (adult, 15%;
    pediatric, at least 2%), Somnolence (adult, 8%; pediatric, 11%)
    Renal: Delay when starting to pass urine (adult, 6%)
    Reproductive: Dysmenorrhea (adult, 3%), Erectile dysfunction
    (adult, 8%)
    Other: Menopausal flushing (adult, 3%)
    Serious
    Cardiovascular: Myocardial infarction, Sudden cardiac death
    Hepatic: Injury of liver (Severe), Liver failure
    Neurologic: Cerebrovascular accident, Dyskinesia, Seizure (adult,
    0.1%; pediatric, 0.2%)
    Psychiatric: Mania, Psychotic disorder, Suicidal thoughts
    (pediatric, 0.4%)
    Reproductive: Priapism (rare)
    Quetiapine (Seroquel) See Seroquel above
    Eszopiclone (Lunesta) See Lunesta above
    Gabapentin (Neurontin) Common
    Cardiovascular: Peripheral edema (1.7% to 8.3%)
    Gastrointestinal: Nausea (greater than 1%), Vomiting (3.3%)
    Immunologic: Viral disease (10.9%)
    Neurologic: Ataxia (Adult, 3%; adult and adolescent, 13%),
    Nystagmus (Adult and adolescent, 8%)
    Other: Fatigue (3% to 11%), Fever (Pediatric, 10%)
    Serious
    Dermatologic: Stevens-Johnson syndrome
    Immunologic: Drug hypersensitivity syndrome
    Neurologic: Dizziness (Adults, 28%; adults and adolescents, 17%;
    pediatrics, 3%), Somnolence (Adults, 21%; adults and adolescents,
    19%; pediatrics, 8%)
    Psychiatric: Disorder of form of thought (Pediatric, 1.7%),
    Disturbance in thinking (2% to 3%), Hostile behavior (Pediatric,
    5.2%), Hyperactive behavior (Pediatric, 4.7%), Mood swings
    (Pediatric, 6%), Suicidal thoughts
    Topiramate (Topamax) Common
    Dermatologic: Flushing (pediatrics, 5%)
    Endocrine metabolic: Serum bicarbonate level abnormal (25% to
    67%)
    Gastrointestinal: Loss of appetite (10% to 24%), Weight decreased
    (4% to 21%)
    Immunologic: Infectious disease (2% to 8%)
    Neurologic: Confusion (3% to 11%), Dizziness (4% to 25%),
    Impaired cognition (2% to 7%), Impaired psychomotor
    performance (2% to 13%), Memory impairment (3% to 12%),
    Paresthesia (1% to 51%), Reduced concentration span (2% to
    10%), Somnolence (6% to 29%)
    Psychiatric: Feeling nervous (4% to 16%), Mood disorder (4% to
    11%)
    Other: Fatigue (6% to 16%), Fever (1% to 12%)
    Serious
    Dermatologic: Erythema multiforme, Stevens-Johnson syndrome,
    Toxic epidermal necrolysis
    Endocrine metabolic: Hyperammonemia (Adolescents, 26%),
    Hypohidrosis, Increased body temperature, Metabolic acidosis
    Hepatic: Liver failure
    Neurologic: Drug-induced encephalopathy
    Ophthalmic: Glaucoma, Myopia, Visual field defect (epilepsy,
    0.1% to 1%)
    Psychiatric: Suicidal thoughts
    Renal: Nephrolithiasis (adults, 1% to 3%)
    Lamotrigine (Lamictal) Common
    Dermatologic: Rash (7% to 14%)
    Gastrointestinal: Abdominal pain (immediate-release, 5% to 10%),
    Diarrhea (immediate-release, 6% to 11%; extended-release, 5%),
    Indigestion (immediate-release, 2% to 7%), Nausea (immediate-
    release, 7% to 25%; extended-release, 7%), Vomiting (immediate-
    release, 5% to 20%; extended-release, 6%))
    Neurologic: Asthenia (immediate-release, 2% to 8%; extended-
    release, 6%), Ataxia (immediate-release, 2% to 11%), Coordination
    problem (immediate-release, 6% to 7%; extended-release, 3%),
    Dizziness (immediate-release, 7% to 54%; extended release, 14%),
    Headache (immediate-release, 29%), Insomnia (immediate-release,
    5% to 10%), Somnolence (immediate-release, 9% to 17%;
    extended-release, 5%), Tremor (immediate-release, 4% to 10%;
    extended-release, 6%), Vertigo (immediate-release, 2%; extended-
    release, 3%)
    Ophthalmic: Blurred vision (immediate-release, 11% to 25%
    (adults) and 4% (children); extended-release, 3%), Diplopia
    (immediate-release, 24% to 49% (adults) and 5% (children);
    extended-release, 5%)
    Psychiatric: Anxiety (immediate-release, 4%; extended-release,
    3%), Depression (immediate-release, 4%; extended-release, 3%)
    Reproductive: Dysmenorrhea (immediate-release, 5% to 7%)
    Respiratory: Rhinitis (immediate-release, 7% to 14%)
    Other: Pain (immediate-release, 5%)
    Serious
    Dermatologic: Erythema multiforme (less than 0.1%), Rash,
    Serious (0.08% to 0.8%), Stevens-Johnson syndrome (0.08% to
    0.8%.), Toxic epidermal necrolysis (0.08% to 0.8%)
    Hematologic: Anemia (immediate release, less than 0.1%),
    Disseminated intravascular coagulation, Eosinophilia (immediate
    release, less than 0.1%), Leukopenia (immediate release, 0.1% to
    1%), Thrombocytopenia (immediate release, less than 0.1%)
    Hepatic: Liver failure
    Immunologic: Drug hypersensitivity syndrome
    Neurologic: Aseptic meningitis
    Other: Angioedema (less than 0.1%), Neuroleptic malignant
    syndrome
    Levetiracetam (Keppra) Common
    Gastrointestinal: Loss of appetite (3% to 8%), Vomiting (15%)
    Immunologic: Infectious disease (13%)
    Musculoskeletal: Decreased bone mineral density (70%), Neck pain
    (2% to 8%)
    Neurologic: Asthenia (15%), Dizziness (5% to 9%), Headache
    (14% to 19%)
    Psychiatric: Abnormal behavior (7% to 37.6%), Irritability (6% to
    12%)
    Respiratory: Cough (2% to 9%), Nasopharyngitis (7% to 15%)
    Other: Fatigue (10% to 11%)
    Serious
    Dermatologic: Stevens-Johnson syndrome, Toxic epidermal
    necrolysis due to drug
    Hematologic: Decreased erythrocyte production, Decreased white
    blood cell count (2.4% to 3.2%), Eosinophilia (8.6%), Neutropenia
    (partial onset seizures, adults, 2.4%), Pancytopenia,
    Thrombocytopenia
    Hepatic: Liver failure
    Neurologic: Somnolence (8% to 45%)
    Psychiatric: Suicidal intent (0.5%), Suicide
    Olanzapine (Zyprexa) Common
    Cardiovascular: Orthostatic hypotension (More than 5%),
    Peripheral edema (3% to 6%)
    Endocrine metabolic: Hypercholesterolemia (Adult, up to 26%;
    adolescent, up to 53%), Hyperglycemia (Adult, up to 20%;
    adolescent, up to 14%), Hyperprolactinemia (30% to 61.1%),
    Increased appetite (Adult, 3% to 24%; adolescent, 17% to 29%),
    Serum triglycerides raised (20.8% to 40%), Weight increased, 7%
    or greater (Adult, 22.2% to 64%; adolescent, 40.6% to 89%)
    Gastrointestinal: Constipation (4% to 11%), Xerostomia (Adult, up
    to 32%; adolescent, 4% to 7%)
    Neurologic: Akathisia (5% to 27%), Asthenia (2% to 20%),
    Dizziness (Adult, 1.6% to 18%; adolescent, 7% to 8%),
    Somnolence (IM, 6%; oral, 20% to 52%), Tremor (1% to 23%)
    Psychiatric: Personality disorder (8%)
    Serious
    Cardiovascular: Sudden cardiac death
    Endocrine metabolic: Diabetes mellitus, Diabetic coma with
    ketoacidosis, Diabetic ketoacidosis, Hyperglycemic hyperosmolar
    state
    Gastrointestinal: Acute hemorrhagic pancreatitis
    Hematologic: Leukopenia, Venous thromboembolism
    Immunologic: Hypersensitivity reaction
    Risperidone (Risperdal) Common
    Dermatologic: Rash (oral, adults, 1% to 4%; pediatrics, up to 11%;
    IM, less than 4%)
    Endocrine metabolic: Hyperprolactinemia (oral, adults, less than
    1%; pediatrics, 49% to 87%; IM, less than 4%), Weight increased
    (oral, adult, 8.7% to 20.9%; pediatric, 14% to 32.6%; IM, adult, 8%
    to 10%)
    Gastrointestinal: Constipation (oral, 8% to 21%; IM, 5% to 7%),
    Diarrhea (oral, 1% to 8%; IM, less than 4%), Excessive salivation
    (oral, 1% to 10%; IM, 1% to 4%), Increased appetite (oral, adult,
    more than 5%; pediatric, 4% to 47%; IM, 4%), Indigestion (oral,
    2% to 10%; IM, 6%), Nausea (oral, 4% to 16%; IM, 3% to 4%),
    Upper abdominal pain (oral, adult, more than 5%; pediatric, 13% to
    16%), Vomiting (oral, 10% to 25%; IM, less than 4%), Xerostomia
    (oral, 4% to 15%; IM, up to 7%)
    Neurologic: Akathisia (oral, up to 10%; IM, 4% to 11%), Dizziness
    (oral, 4% to 16%; IM, 3% to 11%), Dystonia (oral, adult, 3% to
    5%; pediatric, 2% to 6%; IM, adult, less than 4%), Parkinsonism
    (oral, 6% to 28%; IM, 8% to 15%), Sedated (oral, adult, 3% to 6%;
    pediatric, 8% to 29%), Tremor (oral, 2% to 12%; IM, 3% to 24%)
    Ophthalmic: Blurred vision (oral, 1% to 7%; IM, 2% to 3%)
    Psychiatric: Anxiety (oral, up to 16% IM, less than 4%)
    Respiratory: Cough (oral, adults, 2%; pediatrics, 24%; IM, 2% to
    4%), Nasal congestion (oral, adult, 4% to 6%; pediatric, 13%),
    Nasopharyngitis (oral, adult, 3% to 4%; pediatric, 21%), Pain in
    throat (oral, adult, more than 5%; pediatric, 3% to 10%), Upper
    respiratory infection (oral, 2% to 8%; IM, 2% and 6%)
    Other: Fatigue (oral, adult, 1% to 3%; pediatric, 18% to 42%; IM,
    3% to 9%), Pain, General (IM, 1% to 4%)
    Serious
    Cardiovascular: Prolonged QT interval, Sudden cardiac death,
    Syncope (oral, up to 1%; IM, up to 2%)
    Endocrine metabolic: Diabetic ketoacidosis, Hypothermia
    Gastrointestinal: Pancreatitis
    Hematologic: Agranulocytosis, Leukopenia, Neutropenia,
    Thrombocytopenia, Thrombotic thrombocytopenic purpura
    Neurologic: Cerebrovascular accident (oral, less than 5%; IM, less
    than 4%), Seizure (oral, 0.3%; IM, 0.3%), Tardive dyskinesia (oral,
    less than 5%; IM, less than 4%)
    Reproductive: Priapism
    Respiratory: Pulmonary embolism
    Other: Neuroleptic malignant syndrome (oral, adults, less than 1%;
    pediatrics, less than 5%)
    Hydrocodone/ Common
    APAP (Generics) Gastrointestinal: Nausea and vomiting
    Neurologic: Dizziness, Lightheadedness, Sedated
    Serious
    Dermatologic: Acute generalized exanthematous pustulosis,
    Stevens-Johnson syndrome, Toxic epidermal necrolysis
    Hematologic: Agranulocytosis, Thrombocytopenia
    Hepatic: Hepatotoxicity, Liver failure
    Respiratory: Respiratory depression
    Tramadol (Ultram) Common
    Dermatologic: Flushing (7.7% to 15.8%), Pruritus (3% to 11.9%)
    Gastrointestinal: Constipation (10% to 46%), Nausea (13% to
    40%), Vomiting (3% to 17%), Xerostomia (1% to 10%)
    Neurologic: Dizziness (7% to 33%), Headache (3% to 32%),
    Insomnia (1% to 10.9%), Somnolence (4% to 25%)
    Serious
    Cardiovascular: Myocardial infarction (0.5% to less than 1%)
    Endocrine metabolic: Hypoglycemia (Very rare)
    Gastrointestinal: Pancreatitis (0.5% to less than 1%)
    Immunologic: Anaphylactoid reaction (less than 1%)
    Neurologic: Seizure
    Respiratory: Dyspnea (less than 5%), Respiratory depression
    Other: Serotonin syndrome (less than 1%)
    Oxycodone/APAP (Percocet) Common
    Gastrointestinal: Constipation (extended-release, 4%), Nausea
    (extended-release, 31%), Vomiting (extended-release, 9%)
    Neurologic: Dizziness (extended-release, 13%), Headache
    (extended-release, 10%), Lightheadedness, Sedated, Somnolence
    (extended-release, 4%)
    Serious
    Cardiovascular: Disorder of pulmonary circulation, Hypotension,
    Shock
    Dermatologic: Acute generalized exanthematous pustulosis,
    Stevens-Johnson syndrome, Toxic epidermal necrolysis
    Hematologic: Agranulocytosis, Neutropenia
    Hepatic: Hepatic necrosis, Hepatotoxicity, Liver failure
    Immunologic: Anaphylaxis, Hypersensitivity reaction
    Respiratory: Apnea, Respiratory arrest, Respiratory depression
    Other: Neonatal Abstinence Syndrome
    Oxycodone (OxyContin) See Oxycodone above
    Codeine/APAP (Tylenol #2) Common
    Gastrointestinal: Nausea, Vomiting
    Neurologic: Dizziness, Lightheadedness, Sedated, Somnolence
    Serious
    Dermatologic: Acute generalized exanthematous pustulosis,
    Stevens-Johnson syndrome, Toxic epidermal necrolysis
    Hematologic: Agranulocytosis, Thrombocytopenia
    Hepatic: Liver failure
    Immunologic: Hypersensitivity reaction
    Respiratory: Respiratory depression
    Alprazolam (Xanax) See Alprazolam above
    Clonazepam (Klonopin) See Clonazepam above
    Diazepam (Valium) See Diazepam above
    Lorazepam (Ativan) Common
    Neurologic: Asthenia (4.2%), Dizziness (6.9%), Sedated (15.9%),
    Unsteadiness present (3.4%)
    Psychiatric: Depression
    Serious
    Endocrine metabolic: Acidosis (less than 1%)
    Psychiatric: Delirium
    Buspirone (Buspar) Common
    Gastrointestinal: Nausea (8%)
    Neurologic: Dizziness (12%), Headache (6%), Somnolence (10%)
    Psychiatric: Feeling nervous (5%)
    Serious
    Cardiovascular: Congestive heart failure (less than 0.1%),
    Myocardial infarction (less than 0.1%)
    Neurologic: Cerebrovascular accident (less than 0.1%)
    Hydroxyzine (Vistaril) Common
    Gastrointestinal: Xerostomia
    Neurologic: Headache, Somnolence
    Escitalopram (Lexapro) Common
    Dermatologic: Diaphoresis (3% to 8%)
    Gastrointestinal: Abdominal pain (2%), Constipation (3% to 6%),
    Diarrhea (6% to 14%), Indigestion (2% to 6%), Nausea (15% to
    18%), Vomiting (up to 3%), Xerostomia (4% to 9%)
    Neurologic: Dizziness (4% to 7%), Headache (24%), Insomnia (7%
    to 14%), Somnolence (4% to 13%)
    Reproductive: Disorder of ejaculation (9% to 14%), Erectile
    dysfunction (3%), Orgasm incapacity (females, 2% to 6%),
    Reduced libido (3% to 7%)
    Other: Fatigue (5% to 8%)
    Serious
    Psychiatric: Depression, worsening, Suicidal thoughts, Suicide
    Other: Serotonin syndrome
    Sertraline (Zoloft) Common
    Gastrointestinal: Constipation (3% to 8%), Diarrhea (13% to 24%),
    Indigestion (6% to 13%), Nausea (13% to 30%), Nausea and
    vomiting (2% to 30%)
    Neurologic: Dizziness (6% to 17%), Headache (25%), Insomnia
    (12% to 28%), Somnolence (2% to 15%), Tremor (5% to 11%)
    Reproductive: Abnormal ejaculation (7% to 19%), Reduced libido
    (up to 11%)
    Other: Fatigue (10% to 16%)
    Serious
    Dermatologic: Stevens-Johnson syndrome
    Endocrine metabolic: Hyponatremia
    Gastrointestinal: Gastrointestinal hemorrhage
    Immunologic: Anaphylaxis
    Musculoskeletal: Rhabdomyolysis
    Neurologic: Seizure (rare)
    Psychiatric: Depression, Exacerbation, Mania (rare), Suicidal
    thoughts (rare), Suicide (rare)
    Other: Serotonin syndrome
    Trazodone (Desyrel) Common
    Gastrointestinal: Constipation (7% to 8%), Diarrhea (up to 9%),
    Nausea (21%), Vomiting (at least 1%), Xerostomia (14% to 33.8%)
    Musculoskeletal: Backache (5%)
    Neurologic: Confusion (up to 5.7%), Dizziness (25%), Headache
    (9.9% to 33%), Insomnia (6.4% to 9.9%), Somnolence (23.9% to
    46%)
    Ophthalmic: Blurred vision (5% to 14.7%)
    Psychiatric: Dream disorder (up to 5.1%), Feeling nervous (6.4% to
    14.8%)
    Other: Fatigue (5.7% to 15%)
    Serious
    Cardiovascular: Cardiac dysrhythmia, Hypotension (3.8% to 7%),
    Prolonged QT interval, Torsades de pointes
    Immunologic: Hypersensitivity reaction (less than 1%)
    Neurologic: Seizure (rare), Serotonin syndrome
    Psychiatric: Suicidal thoughts (rare), Suicide
    Reproductive: Priapism
    Duloxetine (Cymbalta) Common
    Cardiovascular: Hypertension (2%)
    Dermatologic: Diaphoresis (Adult, 6%; pediatric, less than 2%)
    Gastrointestinal: Constipation (9% to 10%), Decrease in appetite
    (6% to 10%), Diarrhea (Adult, 9%; pediatric, 6%), Nausea (18% to
    23%), Xerostomia (Adult, 11% to 14%; pediatric, 2%)
    Neurologic: Asthenia, Dizziness (Adult, 9%; pediatric, 8%),
    Headache (Adult, 13% to 14%; pediatric, 18%), Hypersomnia,
    Insomnia (7% to 10%), Sedated, Somnolence
    Other: Fatigue
    Serious
    Cardiovascular: Hypertensive crisis, Myocardial infarction (0.01%
    to 0.001%), Orthostatic hypotension
    Dermatologic: Stevens-Johnson syndrome
    Gastrointestinal: Gastrointestinal hemorrhage
    Hematologic: Bleeding, Abnormal
    Hepatic: Liver failure
    Psychiatric: Suicidal thoughts
    Other: Serotonin syndrome, Withdrawal sign or symptom (1% or
    greater)
    Citalopram (Celexa) Common
    Dermatologic: Diaphoresis (5% to 18%)
    Gastrointestinal: Constipation (13%), Diarrhea (8%), Nausea (20%
    to 21%), Vomiting (4% to 20%), Xerostomia (17% to 20%)
    Neurologic: Dizziness (14%), Headache (18%), Insomnia (15%),
    Sedated (15%), Somnolence (18%), Tremor (8% to 16%)
    Psychiatric: Agitation (3% to 10%)
    Reproductive: Disorder of ejaculation (6.1%)
    Other: Fatigue (5%)
    Serious
    Cardiovascular: Myocardial infarction (0.1% to 1%), Prolonged QT
    interval (0.5% to 1.9%), Torsades de pointes
    Neurologic: Cerebrovascular accident (0.1% to less than 1%)
    Psychiatric: Suicidal thoughts, Suicide
    Other: Serotonin syndrome
    Aripiprazole (Abilify) Common
    Endocrine metabolic: Weight increased, 7% or greater (2.5% to
    21.5%)
    Gastrointestinal: Constipation (5% to 11%), Nausea (8% to 15%),
    Vomiting (3% to 11%)
    Neurologic: Akathisia (2% to 25%), Dizziness (4% to 10%),
    Extrapyramidal sign (2% to 27.3%), Headache (10% to 27%),
    Insomnia (8% to 18%), Sedated (3% to 21%), Somnolence (6% to
    26.3%), Tremor (2% to 11.8%)
    Ophthalmic: Blurred vision (3% to 8%)
    Psychiatric: Anxiety (4% to 17%), Restlessness (2% to 12%)
    Other: Fatigue (2% to 17%)
    Serious
    Cardiovascular: Cardiorespiratory arrest (0.1% to 1%),
    Cardiorespiratory failure (0.1% to 1%), Myocardial infarction
    (0.1% to 1%), Prolonged QT interval (0.1% to 1%)
    Endocrine metabolic: Diabetic ketoacidosis (Less than 0.1%)
    Gastrointestinal: Pancreatitis (Lss than 0.1%)
    Hematologic: Agranulocytosis, Leukopenia (Less than 1%),
    Neutropenia (Less than 1%)
    Musculoskeletal: Rhabdomyolysis (Less than 0.1%)
    Neurologic: Cerebrovascular accident, Seizure (Up to 0.3%),
    Tardive dyskinesia, Transient ischemic attack
    Psychiatric: At risk for suicide, Suicidal behavior
    Other: Angioedema (0.1% to less than 1%), Increased body
    temperature, Neuroleptic malignant syndrome
    Paroxetine (Paxil) Common
    Cardiovascular: Palpitations (up to 3%), Vasodilatation (2% to 4%)
    Dermatologic: Diaphoresis (5% to 14%)
    Gastrointestinal: Constipation (up to 16%), Diarrhea (up to 18%),
    Loss of appetite (up to 9%), Nausea (up to 26%), Xerostomia (9%
    to 18%)
    Neurologic: Asthenia (up to 22%), Dizziness (6% to 14%),
    Headache (17% to 27%), Insomnia (up to 24%), Somnolence (up to
    24%), Tremor (4% to 11%)
    Ophthalmic: Blurred vision (up to 5%)
    Reproductive: Abnormal ejaculation (13% to 28%), Erectile
    dysfunction (2% to 9%), Orgasm disorder (females; 2% to 9%),
    Reduced libido (males: 6% to 15%; females: 0% to 9%)
    Respiratory: Yawning (4%)
    Serious
    Dermatologic: Stevens-Johnson syndrome, Toxic epidermal
    necrolysis
    Hepatic: Acute hepatitis (rare)
    Neurologic: Seizure (0.1%)
    Psychiatric: Depression, exacerbation, Suicidal thoughts (rare),
    Suicide (rare)
    Other: Serotonin syndrome
    Fluoxetine (Prozac) Common
    Gastrointestinal: Diarrhea (8% to 18%), Indigestion (6% to 10%),
    Loss of appetite (3.8% to 17%), Nausea (12% to 29%), Xerostomia
    (4% to 12%)
    Neurologic: Asthenia (7% to 21%), Dizziness (2% to 11%),
    Insomnia (9% to 33%), Somnolence (5% to 17%), Tremor (3% to
    13%)
    Psychiatric: Anxiety (3% to 15%), Feeling nervous (3% to 14%)
    Respiratory: Pharyngitis (3% to 11%), Rhinitis (16% to 23%)
    Other: Influenza-like symptoms (3% to 12%)
    Serious
    Cardiovascular: Prolonged QT interval
    Dermatologic: Erythema multiforme
    Endocrine metabolic: Hyponatremia
    Hematologic: Bleeding
    Immunologic: Anaphylactoid reaction
    Neurologic: Seizure (0.2%)
    Psychiatric: Depression, worsening, Mania, Suicidal thoughts,
    Suicide
    Other: Serotonin syndrome
    Venlafaxine (Effexor) Common
    Cardiovascular: Hypertension (3% to 13%)
    Dermatologic: Sweating symptom (6.7% to 25%)
    Endocrine metabolic: Weight loss (3% to 47%)
    Gastrointestinal: Constipation (8% to 15%), Loss of appetite (8% to
    22%), Nausea (21% to 58%), Xerostomia (12% to 22%)
    Neurologic: Asthenia (8% to 19%), Dizziness (11% to 23.9%),
    Dream disorder (3% to 7%), Headache (25% to 38%), Insomnia
    (14% to 24%), Somnolence (14% to 26%), Tremor (1.1% to
    10.2%)
    Ophthalmic: Blurred vision (4% to 6%)
    Psychiatric: Feeling nervous (4% to 21.3%)
    Reproductive: Abnormal ejaculation (2.2% to 19%), Erectile
    dysfunction (2.1% to 6%), Orgasm disorder (2% to 5%)
    Serious
    Endocrine metabolic: Hyponatremia
    Gastrointestinal: Gastrointestinal hemorrhage (rare)
    Hematologic: Bleeding, Abnormal
    Hepatic: Hepatitis
    Neurologic: Seizure (0.3%)
    Psychiatric: Depression, exacerbation (rare), Hypomania, Mania,
    Suicidal thoughts (rare), Suicide
    Other: Neuroleptic malignant syndrome, Serotonin syndrome
    Amitriptyline (Elavil) Common
    Endocrine metabolic: Weight gain
    Gastrointestinal: Constipation, Xerostomia
    Neurologic: Dizziness, Headache, Somnolence
    Ophthalmic: Blurred vision
    Serious
    Cardiovascular: Cardiac dysrhythmia, Electrocardiogram abnormal,
    Myocardial infarction, Prolonged QT interval, Sudden cardiac
    death
    Hematologic: Agranulocytosis
    Hepatic: Hepatotoxicity, Jaundice (rare)
    Neurologic: Neuroleptic malignant syndrome, Seizure
    Psychiatric: Depression, worsening, Suicidal thoughts, Suicide
    Bupropion (Wellbutrin) Common
    Cardiovascular: Tachycardia (major depressive disorder, 11%)
    Endocrine metabolic: Weight gain (2% to 9%), Weight loss (major
    depressive disorder, 14% to 19%)
    Gastrointestinal: Abdominal pain (2% to 9%), Constipation (5% to
    10%), Nausea (13% to 18%), Xerostomia (17% to 26%)
    Neurologic: Confusion (major depressive disorder, 8%), Dizziness
    (6% to 11%), Headache (25% to 34%), Insomnia (11% to 20%)
    Psychiatric: Agitation (2% to 9%)
    Respiratory: Nasopharyngitis (seasonal affective disorder, 13%),
    Pharyngitis (major depressive disorder, 3% to 11%), Upper
    respiratory infection (seasonal affective disorder, 9%)
    Serious
    Cardiovascular: Complete atrioventricular block, Myocardial
    infarction
    Gastrointestinal: Colitis, Pancreatitis
    Hematologic: Pancytopenia
    Hepatic: Abnormal liver function, Hepatitis, Jaundice, Liver
    damage
    Immunologic: Anaphylactoid reaction, Anaphylaxis, Delayed
    hypersensitivity disorder
    Musculoskeletal: Rhabdomyolysis
    Neurologic: Seizure (major depressive disorder, 0.1% to 0.4%)
    Psychiatric: Delusional disorder, Depression, Worsening,
    Hallucinations, Hostile behavior (major depressive disorder, 6%),
    Hypomania, Mania, Precipitation of episode, Paranoid ideation,
    Psychotic disorder, Activation, Suicidal behavior, Suicidal thoughts
    Respiratory: Pulmonary embolism
    Other: Angioedema
    Nortriptyline (Pamelor) Common
    Gastrointestinal: Constipation
    Serious
    Cardiovascular: Cardiac dysrhythmia, Heart block, Myocardial
    infarction, Prolonged QT interval, Sudden cardiac death
    Endocrine metabolic: Syndrome of inappropriate antidiuretic
    hormone secretion
    Gastrointestinal: Paralytic ileus
    Hematologic: Bone marrow depression
    Hepatic: Fulminant hepatic failure, Jaundice (rare)
    Neurologic: Cerebrovascular accident, Myoclonus, Seizure
    Psychiatric: Depression, worsening, Mania, Psychotic disorder,
    exacerbation, Suicidal thoughts, Suicide
    Other: Angioedema
    Mirtazepine (Remeron) Common
    Endocrine metabolic: Increased appetite (17%), Serum triglycerides
    raised (increases to 500 mg/dL or greater: 6%), Weight gain (body
    weight increase of 7% or greater: adults 7.5%; pediatrics 49%)
    Gastrointestinal: Constipation (13%), Xerostomia (25%)
    Hepatic: ALT/SGPT level raised (2%)
    Neurologic: Asthenia (8%), Dizziness (7%), Somnolence (54%)
    Psychiatric: Disturbance in thinking (3%)
    Serious
    Hematologic: Agranulocytosis, Neutropenia
    Hepatic: Cirrhosis of liver (less than 0.1%)
    Neurologic: Grand mal seizure (less than 0.1%), Status epilepticus
    Psychiatric: Depression, exacerbation, Suicidal thoughts, Suicide
    Other: Neuroleptic malignant syndrome, Serotonin syndrome (less
    than 0.1%)
    Olanzapine (Zyprexa) See Olanzapine above
    Risperidone (Risperdal) See Resperidone above
    Antiepileptics
    Divalproex (Depakote) Common
    Gastrointestinal: Abdominal pain (9% to 23%), Diarrhea (13% to
    23%), Indigestion (8% to 11%), Loss of appetite (4% to 12%),
    Nausea (26% to 48%), Vomiting (15% to 27%)
    Musculoskeletal: Backache (Complex partial seizures, greater than
    1% to less than 5%; migraine, 8%)
    Neurologic: Asthenia (6% to 27%), Dizziness (up to 25%), Feeling
    nervous (up to 11%), Headache (31%), Insomnia (up to 15%),
    Somnolence (Adult, 7% to 30%; pediatric, greater than 5%),
    Tremor (1% to 57%)
    Ophthalmic: Amblyopia, Blurred vision, Diplopia (16%)
    Other: Infectious disease (12% to 20%), Influenza (12%)
    Serious
    Cardiovascular: Palpitations (greater than 1% to less than 5%),
    Tachycardia (greater than 1% to less than 5%)
    Endocrine metabolic: Hyperammonemia
    Gastrointestinal: Pancreatitis (greater than 1% to less than 5%)
    Hematologic: Myelodysplastic syndrome, Thrombocytopenia,
    Dose-related (1% to 27%)
    Hepatic: Liver failure
    Immunologic: Drug hypersensitivity syndrome (rare)
    Neurologic: Hyperammonemic encephalopathy
    Otic: Ototoxicity - deafness (greater than 1% to less than 5%)
    Ropinirole (Requip) Common
    Cardiovascular: Hypotension (2% to 25%), Orthostatic hypotension
    (Up to 23%)
    Gastrointestinal: Abdominal pain (6% to 7%), Constipation (4% to
    5%), Nausea (11% to 60%), Vomiting (7% to 12%)
    Neurologic: Dizziness (Parkinson disease, 6% to 40%; restless legs
    syndrome, 11%), Dyskinesia (13% to 34%), Headache (6%),
    Somnolence (Parkinson disease, 7% to 40%; restless leg syndrome,
    12%)
    Other: Fatigue (8% to 11%)
    Serious
    Cardiovascular: Sinus node dysfunction, Syncope (Parkinson
    disease, 1% to 12%; restless leg syndrome, 1%)
    Neurologic: Sleep attack
    Psychiatric: Hallucinations (5% to 10%)
    Pramipexole (Mirapex) Common
    Cardiovascular: Orthostatic hypotension (Immediate release, 53%;
    extended-release, 3%)
    Gastrointestinal: Constipation (immediate-release, 4% to 14%;
    extended-release, 7% to 14%), Nausea (immediate-release, 11% to
    28%; extended-release, 11% to 22%)
    Neurologic: Amnesia (4% to 6%), Asthenia (Immediate-release,
    10% to 14%; extended-release, 3%), Confusion (4% to 10%),
    Dizziness (Immediate-release, 3% to 26%; extended-release, 2% to
    12%), Dream disorder (Up to 11%), Dyskinesia (Immediate-
    release, 18% to 47%; extended-release, 17%), Extrapyramidal
    movements (28%), Headache (Immediate-release, 4% to 16%;
    extended-release, 7%), Insomnia (Immediate-release, 4% to 27%;
    extended-release, 4%)
    Psychiatric: Hallucinations (5% to 17%)
    Serious
    Cardiovascular: Heart failure
    Dermatologic: Malignant melanoma
    Neurologic: Sleep attack (2% to 6%), Somnolence (Immediate-
    release, 6% to 33%;; extended-release, 15% to 36%)
    Psychiatric: Disturbance in thinking, Psychotic disorder
    Other: Malignant melanoma, Neuroleptic malignant syndrome
    Methylphenidate (Concerta) See Methylphenidate above
    Lisdexamfetamine (Vyvanse) Common
    Dermatologic: Rash (pediatrics, 3%)
    Endocrine metabolic: Decreased body growth, Weight decreased
    (pediatrics, 9%)
    Gastrointestinal: Diarrhea (adults, 7%), Loss of appetite (adults, 8%
    to 27%; pediatrics, 34% to 39%), Nausea (adults, 7%; pediatrics,
    6%), Upper abdominal pain (pediatrics, 12%), Vomiting
    (pediatrics, 9%), Xerostomia (Adults, 26% to 36%; pediatrics, 4%
    to 5%)
    Neurologic: Dizziness (pediatrics, 5%), Insomnia (Adults, 20% to
    27%; pediatrics, 13% to 23%)
    Psychiatric: Anxiety (Adults, 5% to 6%), Irritability (pediatrics,
    10%)
    Serious
    Cardiovascular: Chest pain, Myocardial infarction, Peripheral
    vascular disease, Raynaud's disease, Sudden cardiac death,
    Tachycardia, Ventricular hypertrophy
    Immunologic: Anaphylaxis
    Neurologic: Cerebrovascular accident, Seizure
    Amphetamine/Dextro- See Adderall above
    amphetamine (Adderall)
    Dalteparin (Fragmin), Common
    Danaparoid (Orgaran) Dermatologic: Hematoma, Injection site (7% to 35%), Injection site
    pain (4.5% to 12%)
    Other: Irritation symptom, Local
    Serious
    Hematologic: Epidural hematoma, Hematoma, Spinal,
    Hemorrhage, Major (up to 13.6%), Hemorrhagic cerebral infarction
    (8%), Intracranial hemorrhage, Subdural hemorrhage, Intrauterine,
    Thrombocytopenia (Non-cancer indications, less than 1%; patients
    with cancer, 10.9% to 13.6%)
    Hepatic: Increased liver function test (up to 4.3%)
    Immunologic: Anaphylactoid reaction (rare)
    Neurologic: Paralysis
    Enoxaparin (Lovenox) Common
    Gastrointestinal: Diarrhea (2.2%), Nausea (2.5% to 3%)
    Hematologic: Anemia (up to 16%), Bleeding, Major (up to 4%),
    Thrombocytopenia (less than 3%)
    Hepatic: Increased liver function test (5.9% to 6.1%)
    Other: Fever (up to 8%)
    Serious
    Cardiovascular: Atrial fibrillation (0.7%), Heart failure (0.95%)
    Dermatologic: Eczematous drug eruption, Skin necrosis
    Hematologic: Hematoma, Hemorrhage (4% to 13%)
    Neurologic: Intracranial hemorrhage (0.8%), Paraplegia
    Respiratory: Pneumonia (0.82%)
    Heparin (various) Common
    Hematologic: Thrombocytopenia (up to 30%)
    Hepatic: Increased liver aminotransferase level
    Serious
    Hematologic: Hemorrhage (5% to 10%), Heparin-induced
    thrombocytopenia (1% to 10%), Heparin-induced
    thrombocytopenia with thrombosis (less than 1%)
    Immunologic: Hypersensitivity reaction
    Neurologic: Non-traumatic spinal subdural hematoma
    Tinzaparin (Innohep) Common
    Dermatologic: Erythema (16%)
    Hepatic: Increased liver function test, Asymptomatic (9% to 13%)
    Neurologic: Pain, Local (16%)
    Other: Irritation symptom, Local (16%)
    Serious
    Hematologic: Bleeding, Major (0.8%), Granulocytopenic disorder
    (rare), Hematoma, spinal/epidural, Pancytopenia (rare),
    Thrombocytopenia (1%), Thrombocytopenia (Severe) (0.13%)
    Immunologic: Anaphylaxis (rare)
    Neurologic: Paralysis
    Reproductive: Priapism (rare)
    Warfarin (Coumadin) Common
    Dermatologic: Alopecia
    Serious
    Cardiovascular: Cholesterol embolus syndrome, Gangrenous
    disorder (less than 0.1%)
    Dermatologic: Tissue necrosis (less than 0.1%)
    Hematologic: Bleeding, Hemorrhage
    Immunologic: Hypersensitivity reaction
    Musculoskeletal: Compartment syndrome
    Neurologic: Intracranial hemorrhage
    Ophthalmic: Intraocular hemorrhage
    Dabigatran (Pradaxa) Common
    Gastrointestinal: Esophagitis, Gastritis, Gastroesophageal reflux
    disease (Atrial fibrillation, 5.5%), Gastrointestinal hemorrhage
    (DVT and pulmonary embolism, 0.7% to 3.1%; nonvalvular atrial
    fibrillation, 6.1%), Gastrointestinal ulcer, Indigestion (DVT and
    pulmonary embolism, 7.5%)
    Hematologic: Bleeding (DVT and pulmonary embolism
    prophylaxis, 10.5%; nonvalvularatrial fibrillation, 16.6%)
    Serious
    Cardiovascular: Myocardial infarction (DVT and pulmonary
    embolism, 0.32% to 0.66%; nonvalvular atrial fibrillation, 0.7%)
    Gastrointestinal: Gastrointestinal hemorrhage, Major (DVT and
    pulmonary embolism, 0.3% to 0.6%; nonvalvular atrial fibrillation,
    1.6%)
    Hematologic: Bleeding, Major (DVT and pulmonary embolism,
    0.3% to 1.4%; nonvalvular atrial fibrillation, 3.3%), Thrombosis
    Immunologic: Anaphylaxis
    Neurologic: Epidural hematoma, Intracranial hemorrhage
    (nonvalvular atrial fibrillation, 0.3%; DVT and pulmonary
    embolism, 0.1%), Traumatic spinal subdural hematoma
    Respiratory: Bleeding, Alveolar
    Rivaroxaban (Xarelto) Common
    Hematologic: Bleeding (Hip/knee replacement, 5.8%;
    DVT/pulmonary embolism, 17.4% to 28.3%)
    Serious
    Cardiovascular: Syncope (1.2%)
    Gastrointestinal: Gastrointestinal hemorrhage (nonvalvular atrial
    fibrillation, 3.1%)
    Hematologic: Bleeding, Major (Nonvalvular atrial fibrillation,
    5.6%; hip/knee replacement, 0.3%; DVT/pulmonary embolism,
    1%), Epidural hematoma, Hematoma, Spinal
    Immunologic: Anaphylaxis, Hypersensitivity reaction
    Other: Drug withdrawal, Stroke and non-CNS embolism
    Apixaban (Eliquis) Common
    Dermatologic: Contusion (1.4% to 2.2%)
    Gastrointestinal: Bleeding gums (Less than 0.1% to 1.4%)
    Hematologic: Hematoma (DVT, 1.3% to 1.5%)
    Reproductive: Menorrhagia (1.4%)
    Respiratory: Epistaxis (DVT and pulmonary embolism, 1.5% to
    3.6%; DVT prophylaxis, 0.1% to less than 1%), Hemoptysis (Less
    than 0.1% to 1.2%)
    Serious
    Gastrointestinal: Gastrointestinal hemorrhage (atrial fibrillation,
    0.83%/year; DVT prophylaxis, 0.1% to less than 1%; DVT and
    pulmonary embolism, 0.1% to less than 1%), Hematochezia (0.1%
    to less than 1%), Rectal hemorrhage (Less than 0.1% to 1%)
    Hematologic: Bleeding (atrial fibrillation, 2.08%/year; DVT
    prophylaxis, 2.88% to 4.83%), Bleeding, Major (0.1% to 2.13%),
    Hemorrhage (0.1% to 1.4%), Hemorrhage, Operative (DVT
    prophylaxis, 0.1% to less than 1%)
    Hepatic: Alkaline phosphatase raised (DVT prophylaxis, 0.1% to
    less than 1%), Liver function tests abnormal (DVT prophylaxis,
    0.1% to less than 1%), Serum bilirubin raised (DVT prophylaxis,
    0.1% to less than 1%)
    Immunologic: Hypersensitivity reaction (atrial fibrillation, less than
    1%)
    Musculoskeletal: Hemorrhage of muscle (Less than 0.1% to less
    than 1%)
    Neurologic: Epidural hematoma, Intracranial hemorrhage (atrial
    fibrillation, 0.33% to 0.34%/year), Non-traumatic spinal subdural
    hematoma, Traumatic spinal subdural hematoma
    Ophthalmic: Conjunctival hemorrhage (0.1% to less than 1%),
    Intraocular hemorrhage (Less than 0.1% to less than 1%), Retinal
    hemorrhage (0.1% to less than 1%)
    Renal: Hematuria (DVT, 1.4% to 2.1%; DVT prophylaxis, 0.1% to
    less than 1%)
    Edoxaban (Savaysa) Common
    Dermatologic: Rash (3.6% to 4.2%)
    Hematologic: Anemia (Nonvalvular atrial fibrillation, 9.6%; DVT
    or pulmonary embolism, 1.7%), Bleeding, Clinically Relevant,
    Nonmajor (Nonvalvular atrial fibrillation, 9.4%; DVT or
    pulmonary embolism, 7.2%)
    Hepatic: Liver function tests abnormal (Nonvalvular atrial
    fibrillation, 4.8%; DVT or pulmonary embolism, 7.8%)
    Serious
    Hematologic: Bleeding, Major (Nonvalvular atrial fibrillation,
    3.1%; DVT or pulmonary embolism, 1.4%)
    Neurologic: Hemorrhagic cerebral infarction (Nonvalvular atrial
    fibrillation, 0.3%), Intracranial hemorrhage (Nonvalvular atrial
    fibrillation, 0.5%; DVT or pulmonary embolism, 0.1%)
    Respiratory: Interstitial lung disease (Nonvalvular atrial fibrillation,
    0.2%)
    Aspirin Serious
    Gastrointestinal: Gastrointestinal ulcer
    Hematologic: Bleeding
    Ophthalmic: Exudative age-related macular degeneration
    Otic: Tinnitus
    Respiratory: Bronchospasm
    Other: Angioedema, Reye's syndrome
    Ticlopidine Common
    Dermatologic: Rash (1% to 11.8%)
    Gastrointestinal: Abdominal pain, Diarrhea, Indigestion, Loss of
    appetite, Nausea
    Hematologic: Hemorrhage, Leukopenia
    Hepatic: Liver function tests abnormal
    Neurologic: Dizziness
    Serious
    Hematologic: Agranulocytosis, Aplastic anemia (rare),
    Granulocytopenic disorder, Neutropenia (2.4%), Pancytopenia,
    Thrombocytopenia, Thrombotic thrombocytopenic purpura (rare)
    Clopidogrel (Plavix ®) Common
    Hematologic: Bleeding, Non-major (3.6% to 5.1%)
    Serious
    Cardiovascular: Coronary artery stent thrombosis
    Dermatologic: Fixed drug eruption
    Gastrointestinal: Colitis, Gastrointestinal hemorrhage (2%; 2.7%
    with aspirin)
    Hematologic: Agranulocytosis (Less than 1%), Aplastic anemia
    (less then 1%), Bleeding, Major (0.8% to 3.7%), Pancytopenia
    (Severe), Thrombotic thrombocytopenic purpura
    Hepatic: Hepatitis, Hepatotoxicity, Liver failure
    Immunologic: Hypersensitivity reaction
    Neurologic: Epidural hematoma, Intracranial hemorrhage
    Ophthalmic: Intraocular hemorrhage (0.05%)
    Other: Drug withdrawal, Rebound effect
    Dipyridamole Common
    Cardiovascular: Chest pain (IV, up to 30%), Electrocardiogram
    abnormal (IV, 0.8% to 7.5%)
    Dermatologic: Flushing (IV, 3.4%), Rash (oral, 2.3%)
    Gastrointestinal: Abdominal discomfort (oral, 6.1%)
    Neurologic: Dizziness (oral, 13.6%; IV, 11.8%), Headache (oral,
    2.3%; IV, 12.2% to 20%)
    Respiratory: Dyspnea (IV, 2.6% to 25%)
    Serious
    Cardiovascular: Angina, Cardiac arrest, Myocardial infarction (IV,
    0.1%), Myocardial ischemia, Ventricular fibrillation, Ventricular
    tachycardia (IV, 0.2%)
    Hepatic: Liver failure
    Immunologic: Hypersensitivity reaction
    Neurologic: Cerebrovascular accident, Seizure
    Respiratory: Bronchospasm (IV, 0.2%)
    Benazepril (Lotensin) Common
    Neurologic: Dizziness (3.6%), Headache (6.2%)
    Respiratory: Cough (1.2%)
    Other: Fatigue (2.4%)
    Serious
    Dermatologic: Stevens-Johnson syndrome (less than 1%)
    Gastrointestinal: Intestinal angioedema
    Hematologic: Agranulocytosis, Neutropenia
    Hepatic: Hepatic necrosis (rare), Increased liver enzymes (rare),
    Jaundice (rare)
    Immunologic: Anaphylactoid reaction
    Renal: Renal impairment
    Other: Angioedema, head and neck (0.5%)
    Captopril (Capoten) Common
    Cardiovascular: Hypotension
    Dermatologic: Rash
    Endocrine metabolic: Hyperkalemia (11%)
    Gastrointestinal: Disorder of taste
    Respiratory: Cough (0.5% to 2%)
    Serious
    Dermatologic: Stevens-Johnson syndrome
    Gastrointestinal: Intestinal angioedema
    Hematologic: Agranulocytosis (0.1% to 0.2%), Neutropenia (0.1%
    to 0.2%)
    Immunologic: Anaphylactoid reaction
    Other: Angioedema (0.1%)
    Enalapril (Vasotec) Common
    Endocrine metabolic: Hyperkalemia (1% to 3.8%)
    Neurologic: Dizziness (4.3% to 7.9%)
    Renal: Serum blood urea nitrogen raised (0.2% (hypertension) to
    20% (hypertension with renal artery stenosis)), Serum creatinine
    raised (0.2% (hypertension) to 20% (hypertension with renal artery
    stenosis))
    Other: Fatigue (3%)
    Serious
    Cardiovascular: Hypotension (0.9% to 6.7%)
    Gastrointestinal: Intestinal angioedema
    Hematologic: Agranulocytosis
    Hepatic: Hepatotoxicity, Liver failure
    Immunologic: Anaphylactoid reaction, during desensitization
    Renal: Acute renal failure, Renal impairment
    Other: Angioedema (0.1% to 1%)
    Fosinopril (Monopril) Common
    Cardiovascular: Hypotension (2.4% to 4.4%)
    Endocrine metabolic: Hyperkalemia (2.6%)
    Gastrointestinal: Nausea and vomiting (1.2% to 2.2%)
    Neurologic: Dizziness (1.6% to 11.9%)
    Respiratory: Cough (2.2% to 9.7%)
    Serious
    Gastrointestinal: Intestinal angioedema
    Hematologic: Agranulocytosis
    Immunologic: Anaphylactoid reaction
    Renal: Acute renal failure, Azotemia, Oliguria
    Other: Angioedema, Head and Neck
    Lisinopril (Prinivil, Zestril) Common
    Cardiovascular: Chest pain, Hypotension (up to 11%), Syncope
    (5% to 7%)
    Neurologic: Dizziness (12% to 19%), Headache
    Respiratory: Cough
    Serious
    Cardiovascular: Hypotension (Severe) (9%)
    Dermatologic: Stevens-Johnson syndrome (1% or more), Toxic
    epidermal necrolysis (1% or more)
    Endocrine metabolic: Hyperkalemia (2.2% to 6%)
    Gastrointestinal: Intestinal angioedema
    Immunologic: Anaphylaxis due to hymenoptera venom, Dialysis
    membrane-induced anaphylactoid reaction
    Renal: Acute renal failure, Renal impairment (2.4%)
    Other: Angioedema, Head and Neck
    Moexipril (Univasc) Common
    Gastrointestinal: Diarrhea (3.1%)
    Neurologic: Dizziness (4.3%)
    Respiratory: Cough (6.1%)
    Other: Influenza-like symptoms
    Serious
    Gastrointestinal: Intestinal angioedema
    Hematologic: Agranulocytosis
    Immunologic: Anaphylaxis due to hymenoptera venom, Dialysis
    membrane-induced anaphylactoid reaction
    Renal: Abnormal renal function
    Other: Angioedema, Head and Neck
    Perindopril (Aceon) Common
    Endocrine metabolic: Hyperkalemia
    Musculoskeletal: Backache (5.8%)
    Neurologic: Asthenia, Dizziness (8.2%), Headache
    Respiratory: Cough (12%)
    Serious
    Cardiovascular: Cardiac arrest, Orthostatic hypotension (0.8%)
    Gastrointestinal: Intestinal angioedema, Pancreatitis
    Hematologic: Agranulocytosis, Bone marrow depression,
    Neutropenia
    Hepatic: Liver failure
    Renal: Acute renal failure
    Other: Angioedema (0.1% to 0.5%)
    Quinapril (Accupril) Common
    Cardiovascular: Chest pain (2.4%), Hypotension (2.9%)
    Gastrointestinal: Nausea and vomiting (1.4% to 2.4%)
    Neurologic: Dizziness (3.9% to 7.7%), Headache (1.7% to 6.9%)
    Respiratory: Cough (2% to 4.3%)
    Other: Fatigue (2.6%)
    Serious
    Gastrointestinal: Intestinal angioedema
    Hematologic: Agranulocytosis
    Immunologic: Anaphylactoid reaction (rare), Anaphylaxis due to
    hymenoptera venom, Dialysis membrane-induced anaphylactoid
    reaction
    Renal: Serum blood urea nitrogen raised (2% to 8%), Serum
    creatinine raised (2% to 11%)
    Other: Angioedema
    Ramipril (Altace) Common
    Cardiovascular: Hypotension (11%)
    Neurologic: Asthenia, Dizziness (2.2% to 4%), Headache (5.4%)
    Respiratory: Cough (8% to 12%)
    Other: Fatigue
    Serious
    Dermatologic: Stevens-Johnson syndrome
    Gastrointestinal: Intestinal angioedema, Pancreatitis
    Hepatic: Hepatic necrosis, Hepatotoxicity
    Immunologic: Anaphylactoid reaction
    Other: Angioedema, Head and Neck
    Trandolapril (Mavik) Common
    Cardiovascular: Hypotension (0.6% to 11%), Syncope (5.9%)
    Endocrine metabolic: Hyperkalemia (0.3% to 5.3%)
    Gastrointestinal: Indigestion (0.3% to 6.4%)
    Neurologic: Dizziness (1.3% to 23%)
    Renal: Serum blood urea nitrogen raised (9%)
    Respiratory: Cough (1.9% to 35%)
    Serious
    Cardiovascular: Cardiogenic shock (3.8%), Intermittent
    claudication (3.8%)
    Gastrointestinal: Intestinal angioedema
    Hematologic: Agranulocytosis
    Immunologic: Anaphylaxis due to hymenoptera venom, Dialysis
    membrane-induced anaphylactoid reaction
    Other: Angioedema
    Candesartan (Atacand) Common
    Cardiovascular: Hypotension (18.8%)
    Musculoskeletal: Backache (3%.)
    Neurologic: Dizziness (less than 5%)
    Respiratory: Pharyngitis (2%), Rhinitis (2%), Upper respiratory
    infection (6%)
    Eprosartan (Teveten) Common
    Gastrointestinal: Abdominal pain
    Musculoskeletal: Myalgia (1.9%)
    Neurologic: Dizziness (3.8%)
    Respiratory: Upper respiratory infection
    Other: Fatigue (1.4%)
    Serious
    Dermatologic: Edema of face (rare)
    Hematologic: Neutropenia (1.3%)
    Irbesartan (Avapro) Common
    Gastrointestinal: Diarrhea, Heartbum
    Neurologic: Headache
    Respiratory: Upper respiratory infection
    Other: Fatigue
    Serious
    Hematologic: Thrombocytopenia
    Hepatic: Cholestasis, Hepatitis
    Musculoskeletal: Rhabdomyolysis
    Renal: Renal failure
    Other: Angioedema, face, lips, throat
    Losartan (Cozaar) Common
    Cardiovascular: Chest pain (12%), Hypotension (7%)
    Endocrine metabolic: Hyperkalemia (7%), Hypoglycemia (14%)
    Gastrointestinal: Diarrhea (15%)
    Hematologic: Anemia (14%)
    Neurologic: Asthenia, Dizziness (3%)
    Respiratory: Cough (10%)
    Other: Fatigue
    Serious
    Hepatic: Hepatotoxicity
    Musculoskeletal: Rhabdomyolysis
    Renal: Acute renal failure
    Other: Angioedema
    Telmisartan (Micardis)) Common
    Respiratory: Cough (1.6% to 15.6%), Upper respiratory infection
    (7%)
    Serious
    Musculoskeletal: Rhabdomyolysis (rare)
    Valsartan (Diovan) Common
    Cardiovascular: Hypotension (5.5% to 6.9%)
    Neurologic: Dizziness (2% to 17%), Headache (greater than 1%)
    Renal: Serum blood urea nitrogen raised (heart failure, 16.6%),
    Serum creatinine raised (hypertension, 0.8%; heart failure, 3.9%;
    post-myocardial infarction, 4.2%)
    Respiratory: Cough
    Serious
    Renal: Acute renal failure
    Other: Angioedema, Face, lips, throat
    Sacubitril/valsartan (Entresto) Common
    Cardiovascular: Hypotension (18%)
    Endocrine metabolic: Hyperkalemia (12%)
    Neurologic: Dizziness (6%)
    Serious
    Renal: Renal failure (5%)
    Other: Angioedema (0.5%)
    Acebutolol (Sectral) Common
    Neurologic: Dizziness (6%), Headache (6%)
    Other: Fatigue (11%)
    Serious
    Cardiovascular: Angina (2%), Bradyarrhythmia (2%), Heart failure
    (2%)
    Hepatic: Hepatotoxicity (rare)
    Immunologic: Anaphylaxis, Systemic lupus erythematosus (rare.)
    Atenolol (Tenormin) Common
    Cardiovascular: Bradyarrhythmia (3% to 18%), Cold extremities
    (12%), Hypotension (4% to 25%)
    Neurologic: Dizziness (13%)
    Psychiatric: Depression (up to 12%)
    Other: Fatigue (up to 26%)
    Serious
    Cardiovascular: Heart failure, Myocardial infarction, Ventricular
    arrhythmia
    Endocrine metabolic: Thyrotoxicosis
    Immunologic: Anaphylaxis, Systemic lupus erythematosus
    Respiratory: Pulmonary embolism (1.2%)
    Other: Withdrawal sign or sy
    Betaxolol (Kerlone) Common
    Cardiovascular: Bradyarrhythmia (5.8% to 8.1%)
    Gastrointestinal: Indigestion (3.9% to 4.7%), Nausea (1.6% to
    5.8%)
    Musculoskeletal: Arthralgia (3.1% to 5.2%), Chest pain (2.4% to
    7.1%)
    Ophthalmic: Burning sensation in eye (30%, ophthalmic)
    Other: Fatigue (2.9% to 9.7%)
    Serious
    Cardiovascular: Atrioventricular block, Myocardial infarction
    Bisoprolol/hydrochlorothiazide Common
    (Ziac) Gastrointestinal: Diarrhea (4.3%)
    Neurologic: Dizziness (5.1%), Headache (4.5%)
    Other: Fatigue (4.6%)
    Serious
    Cardiovascular: Heart failure
    Ophthalmic: Angle-closure glaucoma, acute, Myopia, Acute
    transient
    Respiratory: Bronchospasm
    Bisoprolol (Zebeta) Common
    Gastrointestinal: Diarrhea (2.6% to 3.5%)
    Neurologic: Headache (8.8% to 10.9%)
    Respiratory: Rhinitis (2.9% to 4%), Upper respiratory infection
    (4.8% to 5%.)
    Other: Fatigue (6.6% to 8.2%)
    Carteolol (Cartrol) Common
    Cardiovascular: Angina
    Neurologic: Asthenia (7%.), Dizziness (4% to 15%.), Headache
    (4% to 17%.), Insomnia (2% to 12%.)
    Ophthalmic: Blurred vision, Burning sensation in eye (25%),
    Conjunctival edema (25%), Conjunctival hyperemia (25%),
    Epiphora (25%), Eye irritation (25%)
    Serious
    Cardiovascular: Cardiac dysrhythmia, Heart failure
    Respiratory: Bronchospasm
    Metoprolol (Lopressor, Toprol Common
    XL) Cardiovascular: Bradyarrhythmia (3%), Cold extremities (1%),
    Heart failure (1%), Hypotension (1%)
    Dermatologic: Pruritus (5%), Rash (5%)
    Gastrointestinal: Constipation (1%), Diarrhea (5%), Indigestion
    (1%), Nausea (1%)
    Neurologic: Dizziness (10%), Fatigue (10%), Headache
    Psychiatric: Depression (5%)
    Respiratory: Dyspnea (3%), Wheezing (1%)
    Serious
    Respiratory: Bronchospasm (1%)
    Nadolol (Corgard) Common
    Cardiovascular: Bradyarrhythmia (2%)
    Neurologic: Dizziness (2%)
    Other: Fatigue (2%)
    Serious
    Cardiovascular: Atrioventricular block, Cardiac dysrhythmia (1%),
    Heart failure (1%)
    Propranolol (Inderal) Common
    Gastrointestinal: Diarrhea, Vomiting
    Neurologic: Dizziness (Hypertension, 4% to 7%), Sleep disorder
    Other: Fatigue (5% to 7%)
    Serious
    Cardiovascular: Bradyarrhythmia, Cardiogenic shock, Congestive
    heart failure, Heart block, Heart failure, Hypotension, Prolonged
    PR interval, Shortened QT interval
    Dermatologic: Erythroderma, Stevens-Johnson syndrome, Toxic
    epidermal necrolysis
    Endocrine metabolic: Hypoglycemia
    Immunologic: Anaphylaxis
    Neurologic: Cerebrovascular accident
    Respiratory: Bronchospasm
    Other: Withdrawal sign or symptom
    Sotalol (Betapace) Common
    Cardiovascular: Chest pain (Adult, 16%; pediatric, 4%),
    Lightheadedness (12%)
    Dermatologic: Rash (5%)
    Neurologic: Disturbance of consciousness (4%), Dizziness (13.1%
    to 20%), Headache (3.3% to 11.5%)
    Respiratory: Dyspnea (9.2% to 21%)
    Other: Fatigue (18.9% to 20%)
    Serious
    Cardiovascular: Atrioventricular block, Bradyarrhythmia (Adult,
    12.3% to 16%; pediatric, 4%), Cardiac dysrhythmia (5%),
    Congestive heart failure (1.2% to 3.3%), Heart failure (5%),
    Prolonged QT interval, Torsades de pointes (0.5% to 4%)
    Neurologic: Cerebrovascular accident (1%)
    Timolol (Blocadren) Common
    Cardiovascular: Angina, Bradyarrhythmia (5% to 9.1%, oral),
    Heart failure (8%, oral), Hypotension
    Dermatologic: Pruritus, Rash, Urticaria
    Gastrointestinal: Abdominal pain, Diarrhea, Indigestion, Nausea,
    Vomiting
    Musculoskeletal: Cramp
    Neurologic: Confusion (13%), Dizziness (2.3% to 6%, oral),
    Headache (1.7%, oral; 1% to 5%, ophthalmic)
    Ophthalmic: Blurred vision (Ophthalmic, 15% to 33%), Burning
    sensation in eye (Ophthalmic, 12.5% to 20%), Dry eyes
    Psychiatric: Depression (9.2%, ophthalmic), Hallucinations (11%),
    Psychotic disorder (3%)
    Respiratory: Cough, Dyspnea (1.7%, oral)
    Other: Fatigue (3.4% to 5%, oral), Infectious disease
    Serious
    Cardiovascular: Cardiac dysrhythmia (1%), Myocardial infarction
    (rare)
    Respiratory: Bronchospasm (0.6%, oral)
    carvedilol, Common brand Common
    names - Coreg* Cardiovascular: Bradyarrhythmia (3% to 10%), Hypotension (1.8%
    to 20.2%), Peripheral edema (1% to 7%)
    Endocrine metabolic: Abnormal weight gain (10% to 12%),
    Hyperglycemia (5% to 12%)
    Gastrointestinal: Diarrhea (2% to 12%)
    Neurologic: Dizziness (6% to 33%)
    Reproductive: Erectile dysfunction (13.5%)
    Other: Fatigue (24%)
    Serious
    Cardiovascular: Atrioventricular block (greater than 1% to 3%)
    Dermatologic: Erythema multiforme, Stevens-Johnson syndrome,
    Toxic epidermal necrolysis
    Hematologic: Aplastic anemia
    Ophthalmic: Intraoperative floppy iris syndrome
    Respiratory: Asthma with status asthmaticus (rare)
    labetolol hydrochloride, Common
    Common brand names Cardiovascular: Orthostatic hypotension (1%, oral; 58%, IV)
    Normodyne*, Trandate* Dermatologic: Has tingling sensation (7%.)
    Gastrointestinal: Nausea (14%)
    Neurologic: Dizziness (9% to 20%)
    Respiratory: Nasal congestion (3%)
    Other: Fatigue (11%)
    Serious
    Cardiovascular: Heart failure
    Endocrine metabolic: Hyperkalemia
    Hepatic: Hepatotoxicity
    Respiratory: Bronchospasm
    Amlodipine (Norvasc, Lotrel) Common
    Cardiovascular: Flushing (0.7% to 2.6%), Palpitations (Up to
    4.5%), Peripheral edema (Up to 10.8%)
    Gastrointestinal: Abdominal pain (1.6%), Nausea (2.9%.)
    Neurologic: Dizziness (Up to 3.4%), Headache (7.3%),
    Somnolence (1.4%)
    Other: Fatigue (4.5%)
    Serious
    Cardiovascular: Acute myocardial infarction, Angina
    Other: Angioedema
    Bepridil (Vascor) Common
    Diarrhea
    Dizzy
    Feel Like Throwing Up
    Infrequent side effects of Vascor:
    Abnormal Heart Rhythm
    Chronic Heart Failure
    Fluid in the Lungs
    Prolonged Q-T Interval on EKG
    Slow Heartbeat
    Very Rapid Heartbeat - Torsades de Pointes
    Head Pain
    Incomplete or Infrequent Bowel Movements
    Low Energy
    Rare side effects of Vascor:
    Deficiency of Granulocytes a Type of White Blood Cell
    Fluid Retention in the Legs, Feet, Arms or Hands
    Inflammation of Skin caused by an Allergy
    Rash
    Reaction due to an Allergy
    Low Blood Pressure
    Diltiazem (Cardizem, Tiazac) Common
    Cardiovascular: Bradyarrhythmia (1.7% to 3.6%), Peripheral
    edema (4.6% to 8%)
    Neurologic: Dizziness (3.5% to 6.4%), Headache (4.6%)
    Respiratory: Cough (2%)
    Other: Fatigue (4.8%)
    Serious
    Cardiovascular: Congestive heart failure (less than 2%), Heart
    block, Myocardial infarction
    Hepatic: Hepatotoxicity
    Felodipine (Plendil) Common
    Cardiovascular: Peripheral edema (2% to 17.4%)
    Dermatologic: Flushing (3.9% to 6.9%)
    Gastrointestinal: Indigestion (0.5% to 3.9%)
    Neurologic: Headache (10.6% to 14.7%)
    Respiratory: Upper respiratory infection (0.7% to 3.9%)
    Serious
    Cardiovascular: Angina, Hypotension (less than 0.5%), Myocardial
    infarction, Tachycardia
    Neurologic: Cerebrovascular accident
    Nifedipine (Adalat, Procardia) Common
    Cardiovascular: Hypotension (up to 5%), Palpitations (up to 7%),
    Peripheral edema (7% to 29%)
    Dermatologic: Flushing (4% to 25%)
    Gastrointestinal: Nausea (up to 10%)
    Neurologic: Dizziness (4% to 10%), Headache (19% to 23%)
    Psychiatric: Feeling nervous
    Respiratory: Cough, Dyspnea
    Serious
    Cardiovascular: Myocardial infarction (up to 4%), Ventricular
    arrhythmia (less than 0.5%)
    Gastrointestinal: Gastrointestinal obstruction, Gastrointestinal ulcer
    Hematologic: Aplastic anemia
    Nimodipine (Nimotop) Common
    Cardiovascular: Hypotension (up to 8.1%)
    Gastrointestinal: Diarrhea (up to 4.2%), Nausea (0.6% to 1.4%)
    Neurologic: Headache (up to 4.1%)
    Serious
    Cardiovascular: Congestive heart failure (less than 1%)
    Gastrointestinal: Gastrointestinal hemorrhage (less than 1%)
    Hematologic: Bleeding, Disseminated intravascular coagulation
    (less than 1%), Hematoma (less than 1%)
    Nisoldipine (Sular) Common
    Cardiovascular: Palpitations (3%), Peripheral edema (22%),
    Vasodilatation (4%)
    Dermatologic: Flushing
    Neurologic: Dizziness (5%), Headache (22%)
    Respiratory: Pharyngitis (5%), Sinusitis
    Serious
    Cardiovascular: Myocardial infarction
    Verapamil (Calan, Isoptin, Common
    Verelan) Cardiovascular: Edema (up to 3.7%), Hypotension (1.5% to 3%)
    Gastrointestinal: Constipation (7.3% to 13%)
    Neurologic: Dizziness (3% to 5.9%), Headache (2.2% to 12.1%)
    Respiratory: Pharyngitis (3%), Sinusitis (3%)
    Other: Influenza-like symptoms (3.7%)
    Serious
    Cardiovascular: Atrioventricular block, Myocardial infarction
    Respiratory: Pulmonary edema
    Digoxin Common
    Gastrointestinal: Nausea and vomiting
    Neurologic: Dizziness, Headache
    Psychiatric: Mental disorder
    Serious
    Cardiovascular: Cardiac dysrhythmia, Ischemia, Sinoatrial block,
    Sinus bradycardia, Vasoconstriction
    Hematologic: Thrombocytopenia
    Digitoxin Common
    Enlarged BreastsLCommon side effects of digitoxin:
    Enlarged Breasts
    Infrequent side effects of digitoxin:
    Sinus Bradycardia
    Rare side effects of digitoxin:
    Abnormal Heart Electrical Signals
    Atrioventricular Heart Block
    Decreased Blood Platelets
    Delirium
    Diarrhea
    Fast Heartbeat
    Gangrene of Intestine caused by Blood Supply ProblemSevere
    Heart Block
    Inflammation of Skin caused by an Allergy
    Loss of Appetite
    Rapid Ventricular Heartbeat
    Rash
    Reaction due to an Allergy
    Throwing Up
    Ventricular Fibrillation
    Ventricular Premature Beats
    Visual Halos Around Lights
    Anxious
    Blurred Vision
    Confused
    Depression E194
    Discolored Spots and Small Elevations of the SkinLess
    DizzyLess
    Feel Like Throwing Up
    Feeling Weak
    Hallucination
    Head Pain
    Lanoxin See Digoxin above
    Amiloride (Midamor) Common
    Dermatologic: Rash (1% or less)
    Gastrointestinal: Diarrhea (3% to 8%), Loss of appetite (3% to 8%),
    Nausea (3% to 8%), Vomiting (3% to 8%)
    Musculoskeletal: Asthenia (greater than 1% to less than 3%),
    Cramp (greater than 1% to less than 3%)
    Neurologic: Dizziness (greater than 1% to less than 3%), Headache
    (3% to 8%)
    Respiratory: Cough (greater than 1% to less than 3%), Dyspnea
    (greater than 1% to less than 3%)
    Serious
    Cardiovascular: Cardiac dysrhythmia (1% or less), Palpitations (1%
    or less)
    Endocrine metabolic: Hyperkalemia (10%)
    Hematologic: Aplastic anemia, Neutropenia
    Neurologic: Encephalopathy (greater than 1% to less than 3%)
    Ophthalmic: Raised intraocular pressure (1% or less)
    Bumetanide (Bumex) Common
    Cardiovascular: Hypotension (0.8%)
    Endocrine metabolic: Hyperuricemia (18.4%), Hypochloremia
    (14.9%), Hypokalemia (14.7%)
    Gastrointestinal: Nausea (0.6%)
    Musculoskeletal: Cramp (1.1%)
    Neurologic: Dizziness (1.1%), Headache (0.6%)
    Renal: Azotemia (10.6%)
    Serious
    Dermatologic: Stevens-Johnson syndrome
    Hematologic: Thrombocytopenia (0.2%)
    Neurologic: Encephalopathy (0.6%)
    Chlorothiazide (Diuril) Common
    Dermatologic: Photosensitivity
    Endocrine metabolic: Hyperglycemia, Hyperuricemia
    Gastrointestinal: Diarrhea, Loss of appetite, Nausea, Vomiting
    Neurologic: Dizziness
    Serious
    Dermatologic: Cutaneous lupus erythematosus, Stevens-Johnson
    syndrome, Toxic epidermal necrolysis
    Endocrine metabolic: Electrolytes abnormal
    Gastrointestinal: Pancreatitis
    Hematologic: Agranulocytosis, Aplastic anemia, Hemolytic anemia
    Hepatic: Hepatotoxicity, Jaundice
    Immunologic: Anaphylaxis, Systemic lupus erythematosus
    Neurologic: Coma
    Renal: Renal failure
    Respiratory: Pulmonary edema, Noncardiogenic
    Chlorthalidone (Hygroton) Common
    Endocrine metabolic: Hyperuricemia
    Serious
    Cardiovascular: Cardiac dysrhythmia
    Dermatologic: Toxic epidermal necrolysis
    Gastrointestinal: Pancreatitis (rare)
    Hepatic: Cholestatic jaundice syndrome
    Respiratory: Pulmonary edema (rare)
    Furosemide (Lasix) Common
    Endocrine metabolic: Hyperuricemia (40%), Hypomagnesemia
    Gastrointestinal: Loss of appetite
    Renal: Spasm of bladder
    Serious
    Cardiovascular: Orthostatic hypotension
    Dermatologic: Drug hypersensitivity syndrome, Erythema
    multiforme, Erythroderma, Stevens-Johnson syndrome, Toxic
    epidermal necrolysis due to drug
    Gastrointestinal: Pancreatitis
    Hematologic: Agranulocytosis, Aplastic anemia,
    Thrombocytopenia
    Immunologic: Anaphylactoid reaction, Anaphylaxis
    Hydro-chlorothiazide (Esidrix, Common
    Hydrodiuril) Cardiovascular: Hypotension
    Dermatologic: Phototoxicity
    Neurologic: Vertigo
    Serious
    Cardiovascular: Cardiac dysrhythmia
    Dermatologic: Stevens-Johnson syndrome, Toxic epidermal
    necrolysis
    Endocrine metabolic: Dilutional hyponatremia, Hypercalcemia,
    Hyperglycemia, Hypokalemia, Hypomagnesemia, Hyponatremia,
    Hypophosphatemia
    Gastrointestinal: Cholecystitis, Pancreatitis
    Hepatic: Cholestatic jaundice syndrome
    Ophthalmic: Angle-closure glaucoma, acute, Myopia, Acute
    transient
    Renal: Renal failure, Renal impairment
    Indapamide (Lozol) Common
    Endocrine metabolic: Hypokalemia (3% to 7%)
    Musculoskeletal: Cramp
    Neurologic: Asthenia, Dizziness (Greater than or equal to 5%),
    Headache (Greater than or equal to 5%), Lethargy, Numbness
    Other: Fatigue, Malaise
    Serious
    Dermatologic: Stevens-Johnson syndrome, Toxic epidermal
    necrolysis
    Hematologic: Agranulocytosis, Aplastic anemia
    Hepatic: Hepatitis
    Immunologic: Anaphylaxis
    Spironolactone (Aldactone) Common
    Endocrine metabolic: Gynecomastia
    Gastrointestinal: Diarrhea, Nausea and vomiting
    Neurologic: Somnolence
    Reproductive: Disorder of menstruation, Erectile dysfunction
    Serious
    Dermatologic: Stevens-Johnson syndrome, Toxic epidermal
    necrolysis
    Endocrine metabolic: Breast cancer, Disorder of electrolytes,
    Hyperkalemia, Metabolic acidosis
    Gastrointestinal: Gastric hemorrhage, Gastritis
    Hematologic: Agranulocytosis
    Immunologic: Drug hypersensitivity syndrome, Systemic lupus
    erythematosus
    Other: Breast cancer
    Isosorbide dinitrate (Isordil) Common
    Cardiovascular: Hypotension, Lightheadedness
    Neurologic: Headache
    Serious
    Cardiovascular: Syncope
    Hematologic: Methemoglobinemia
    Nesiritide (Natrecor) Common
    Cardiovascular: Hypotension (4% to 17%)
    Gastrointestinal: Nausea (3%)
    Neurologic: Dizziness (2%), Headache (7%)
    Renal: Serum creatinine raised (17% to 31.4%)
    Serious
    Dermatologic: Injection site extravasation
    Immunologic: Hypersensitivity reaction
    Other: Death, Increased risk
    Hydralazine (Apresoline) Common
    Cardiovascular: Angina, Edema, Palpitations, Tachycardia
    Gastrointestinal: Diarrhea, Loss of appetite, Nausea, Vomiting
    Neurologic: Headache
    Serious
    Hematologic: Agranulocytosis, Leukopenia
    Hepatic: Hepatotoxicity
    Immunologic: Lupus pneumonia (Acute), Systemic lupus
    erythematosus
    Nitrates (Nitroglycerin) Common
    Cardiovascular: Hypotension (4%)
    Dermatologic: Flushing
    Neurologic: Dizziness (5%), Headache (63% to 64%),
    Lightheadedness (6%)
    Serious
    Dermatologic: Anaphylactoid reaction
    Hematologic: Methemoglobinemia
    Neurologic: Raised intracranial pressure
    Minoxidil Common
    Cardiovascular: Hypotension
    Dermatologic: Hirsutism, Hypertrichosis
    Endocrine metabolic: Body fluid retention (7%), Hypernatremia
    Serious
    Cardiovascular: Angina, Cardiac tamponade, Electrocardiogram
    abnormal (60%), Pericardial effusion (3%), Pericarditis,
    Tachyarrhythmia
    Dermatologic: Stevens-Johnson syndrome
    Hematologic: Leukopenia, Thrombocytopenia
  • Table 5 is included by reference as the drugs that are listed as in development in the following databases: Cortellis™ Competitive Intelligence by Thomson Reuters; Adis R&D; and Pharmaprojects by Citeline. The drugs in the development pipeline can utilize the Invention to capture required clinical trial information and control drug dispensing for regulatory drug approval as well as to control drug dispensing after regulatory approval. The drugs are encompassed in the embodiment of the invention by reference. The listing for each drug includes by definition each drug's respective indication(s), strength, dosage form, route of administration, side effect profile, drug interactions, etc.
  • Table 6 is included by reference as the mechanisms of action for marketed drugs, drugs in developed, and efficacious drugs whose development was stopped due to a side effect(s) that can be addressed by the embodiment and thereby made approvable. The listed drugs in the following databases are encompassed in the embodiment of the invention by reference: Cortellis™ Competitive Intelligence by Thomson Reuters; Adis R&D; and Pharmaprojects by Citeline. The listing for each includes by definition each respective drug's respective indication(s), strength, dosage form, route of administration, side effect profile, drug interactions, etc.
  • Table 7 is included by reference as the oral drugs listed in the following databases that (i) were in development but were disconintued due to dose related side effects whose safety concerns can be addressed by the Invention or (ii) drugs that were withdrawn from the market after approval due to dose related side effects whose safety concerns can be addressed by the Invention: Cortellis™ Competitive Intelligence by Thomson Reuters; Adis R&D; and Pharmaprojects by Citeline. These drugs are encompassed in the embodiment of the invention by reference. The listing for each drug includes by definition each drug's respective indication(s), strength, dosage form, route of administration, side effect profile, drug interactions, etc.
  • Table 8 is a sample list of diseases encompassed in the embodiment of the invention by reference. The listing for each encompasses drugs used to treat the disease and for each includes by definition each drug's respective indication(s), strength, dosage form, route of administration, side effect profile, drug interactions, etc.
  • TABLE 8
    Diseases
    Abdominal Aortic Aneurysm - see Aortic Aneurysm
    ACE (Adverse Childhood Experiences)
    Acinetobacter Infection
    Acquired Immune Deficiency Syndrome (AIDS) - see HIV/AIDS
    Acquired Immunodeficiency Syndrome (AIDS) - see HIV/AIDS
    Adenovirus Infection
    Adenovirus Vaccination
    ADHD [Attention Deficit/Hyperactivity Disorder]
    Adult Vaccinations
    Adverse Childhood Experiences (ACE)
    African Trypanosomiasis - see Sleeping Sickness
    Agricultural Safety - see Farm Worker Injuries
    AHF (Alkhurma hemorrhagic fever)
    AIDS (Acquired Immune Deficiency Syndrome)
    AIDS (Acquired Immunodeficiency Syndrome)
    Alkhurma hemorrhagic fever (AHF)
    ALS [Amyotrophic Lateral Sclerosis]
    Alzheimer's Disease
    Amebiasis, Intestinal [Entamoeba histolytica infection]
    American Indian and Alaska Native Vaccination
    American Trypanosomiasis - see Chagas Disease
    Amphibians and Fish, Infections from - see Fish and Amphibians,
    Infections from
    Amyotrophic Lateral Sclerosis - see ALS
    Anaplasmosis, Human
    Ancylostoma duodenale Infection, Necator americanus Infection -
    see Human Hookworm
    Anemia
    Angiostrongylus Infection
    Animal-Related Diseases
    Anisakiasis - see Anisakis Infection
    Anisakis Infection [Anisakiasis]
    Anthrax [Bacillus anthracis Infection]
    Anthrax Emergency Vaccination
    Antibiotic and Antimicrobial Resistance
    Antibiotic Use, Appropriate
    Aortic Aneurysm
    Aortic Dissection - see Aortic Aneurysm
    Arenavirus Infection
    Arthritis
    Ascariasis - see Ascaris Infection
    Ascaris Infection [Ascariasis]
    ASDs (Autism and Genetics)
    Aseptic Meningitis - see Viral Meningitis
    Aspergillosis - see Aspergillus Infection
    Aspergillus Infection [Aspergillosis]
    Asthma
    Attention Deficit/Hyperactivity Disorder - see ADHD
    Autism
    Autism and Genetics (ASDs) [autism spectrum disorders]
    autism spectrum disorders - see Autism and Genetics
    Avian Influenza
    B virus Infection [Herpes B virus]
    B. cepacia infection (Burkholderia cepacia Infection)
    Babesia Infection - see Babesiosis
    Babesiosis [Babesia Infection]
    Bacillus anthracis - see Anthrax
    Bacillus anthracis Infection - see Anthrax
    Back Belts - see Ergonomic and Musculoskeletal Disorders
    Bacterial Meningitis
    Bacterial Vaginosis (BV)
    Balamuthia mandrillaris Infection - see Balamuthia Infection
    Balamuthia Infection [Balamuthia mandrillaris Infection]
    Balantidiasis - see Balantidium Infection
    Balantidium Infection [Balantidiasis]
    Bartonella bacilliformis Infection - see Carrión's disease
    Bartonella quintana Infection - see Trench fever
    Baylisascaris Infection - see Raccoon Roundworm Infection
    BCG (Tuberculosis Vaccine)
    Bilharzia - see Schistosomiasis
    Bioterrorism Agents/Diseases
    Bird Flu - see Avian Influenza
    Birth Defects
    Black Lung [Coal Workers' Pneumoconioses]
    Blast Injuries
    Blastocystis hominis Infection - see Blastocystis Infection
    Blastocystis Infection [Blastocystis hominis Infection]
    Blastomycosis [Blastomyces dermatitidis Infection]
    Bleeding Disorders
    blood clot
    Blood Disorders
    Body Lice [Pediculus humanus corporis]
    Bone Health
    Borrelia burgdorferi Infection - see Lyme Disease
    Botulism [Clostridium botulinim Infection]
    Bovine Spongiform Encephalopathy (BSE)
    Brainerd Diarrhea
    Breast and Ovarian Cancer and Family Health History
    Breast Cancer
    Breastfeeding
    Bronchiolitis - see Respiratory Syncytial Virus Infection
    Bronchitis
    Brucella Infection [Brucellosis]
    Brucellosis - see Brucella Infection
    BSE (Bovine Spongiform Encephalopathy)
    BSE (Mad Cow Disease)
    Burkholderia cepacia Infection (B. cepacia infection)
    Burkholderia mallei - see Glanders
    Burkholderia pseudomallei Infection - see Melioidosis
    BV (Bacterial Vaginosis)
    C. diff. Infection [Clostridium difficile Infection]
    C. gattii cryptococcosis
    C. neoformans cryptococcosis
    Campylobacter Infection [Campylobacteriosis]
    Campylobacteriosis - see Campylobacter Infection
    Cancer
    Cancer and Flu
    Cancer Health Disparities - see Health Disparities in Cancer
    Candida Infection [Candidiasis]
    Candidiasis - see Candida Infection
    Canine Flu
    Capillaria Infection [Capillariasis]
    Capillariasis - see Capillaria Infection
    Carbapenem resistant Klebsiella pneumonia (CRKP) see
    Klebsiella pneumoniae
    Carbapenem-resistant Enterobacteriaceae (CRE)
    Cardiovascular Health - see Heart Disease
    Carpal Tunnel Syndrome - see Ergonomic and Musculoskeletal
    Disorders
    Carrión's disease [Bartonella bacilliformis Infection]
    Cat Flea Tapeworm - see Tapeworm, Dog and Cat Flea
    Cats, Infections from
    CCHF (Crimean-Congo hemorrhagic fever)
    Cercarial Dermatitis - see Swimmer's Itch
    Cerebral Palsy
    Cervical Cancer
    CFS (Chronic Fatigue Syndrome)
    Chagas Disease [Trypanosoma cruzi Infection]
    Chapare Hemorrhagic Fever (CHHF)
    Chest Cold - see Bronchitis
    CHHF (Chapare Hemorrhagic Fever)
    Chickenpox [Varicella Disease]
    Chickenpox Vaccination
    Chikungunya Fever (CHIKV)
    CHIKV (Chikungunya Fever)
    Childhood Arthritis
    Childhood Injuries
    Childhood Overweight and Obesity
    Children's Cough and Cold Medicines - see Cough and Cold
    Medicines
    Chlamydia [Chlamydia trachomatis Disease]
    Chlamydia trachomatis Disease - see Chlamydia
    Chlamydophila (Chlamydia) pneumoniae Infection
    Cholera [Vibrio cholerae Infection]
    Chronic Disease Prevention
    Chronic Fatigue Syndrome (CFS)
    Chronic Kidney Disease (CKD)
    Chronic Obstructive Pulmonary Disease (COPD)
    Chronic Wasting Disease (CWD)
    Ciguatera Fish Poisoning
    Ciguatoxin - see Marine Toxins
    CJD, Classic (Classic Creutzfeldt-Jakob Disease)
    CKD (Chronic Kidney Disease)
    CKD (Kidney Disease)
    Classic Creutzfeldt-Jakob Disease (CJD, Classic)
    Clonorchiasis - see Clonorchis Infection
    Clonorchis Infection [Clonorchiasis]
    Clostridium botulinim Infection - see Botulism
    Clostridium difficile Infection - see C. diff. Infection
    Clostridium perfringens infection
    Clostridium perfringens infection
    Clostridium tetani Infection - see Tetanus Disease
    Clotting Disorders
    CMV (Cytomegalovirus Infection)
    Coal Workers' Pneumoconioses - see Black Lung
    Coccidioidomycosis - see Valley Fever
    Cold, Common
    Colorado Tick Fever (CTF)
    Colorectal (Colon) Cancer
    Colorectal Cancer and Genetics
    Colorectal Cancer Control Program (CRCCP)
    Common Cold - see Cold, Common
    Concussion - see Traumatic Brain Injury
    Congenital Hearing Loss - see Hearing Loss in Children
    Conjunctivitis - see Pink Eye
    Cooleys Anemia
    COPD (Chronic Obstructive Pulmonary Disease)
    Corynebacterium diphtheriae Infection - see Diphtheria
    Cough and Cold Medicines
    Coxiella burnetii Infection - see Q Fever
    CRE (Carbapenem-resistant Enterobacteriaceae)
    Creutzfeldt-Jakob Disease, Classic - see Classic Creutzfeldt-Jakob
    Disease
    Crimean-Congo hemorrhagic fever (CCHF) [Nairovirus Infection]
    CRKP (Carbapenem resistant Klebsiella pneumonia)
    Crohn's Disease - see Inflammatory Bowel Disease
    Cronobacter Infection
    Cryptococcosis, C. gattii. - see C. gattii cryptococcosis
    Cryptococcosis, C. neoformans - see C. neoformans cryptococcosis
    Cryptosporidiosis - see Cryptosporidium Infection
    Cryptosporidium Infection [Cryptosporidiosis]
    CTF (Colorado Tick Fever)
    CWD (Chronic Wasting Disease)
    Cyclospora Infection [Cyclosporiasis]
    Cyclosporiasis - see Cyclospora Infection
    Cysticercosis
    Cystoisospora Infection [Cystoisosporiasis]
    Cystoisosporiasis - see Cystoisospora Infection
    Cytomegalovirus Infection (CMV)
    DBA (Diamond Blackfan Anemia)
    Deep Vein Thrombosis (DVT)
    Dengue Fever (DF)
    Dengue Hemorrhagic Fever (DHF) - see Dengue Fever
    Dermatophyte Infection - see Ringworm
    Dermatophytes - see Ringworm
    Developmental Disabilities
    DF (Dengue Fever)
    DHF (Dengue Hemorrhagic Fever)
    Diabetes
    Diamond Blackfan Anemia (DBA)
    Dientamoeba fragilis Infection
    Diet and Nutrition - see Nutrition
    Diphtheria [Corynebacterium diphtheriae Infection]
    Diphtheria Vaccination
    Diphyllobothriasis - see Diphyllobothrium Infection
    Diphyllobothrium Infection [Diphyllobothriasis]
    Dipylidium Infection - see Tapeworm, Dog and Cat Flea
    Dirofilariasis (Dog Heartworm)
    Division of Public Health Systems and Workforce Development
    (DPHSWD)
    Division of Public Health Systems and Workforce Development
    (DPHSWD) - see Division of Public Health Systems and Workforce
    Development
    Dog Flea Tapeworm - see Tapeworm, Dog and Cat Flea
    Dog Heartworm [Dirofilaria] - see Dirofilariasis (Dog Heartworm)
    Dogs, Infections from
    Down Syndrome [Trisomy 21]
    DPHSWD (Division of Public Health Systems and Workforce
    Development)
    Dracunculiasis - see Guinea Worm Disease
    Drug Resistance - see Antibiotic and Antimicrobial Resistance
    DVT (Deep Vein Thrombosis)
    Dwarf Tapeworm [Hymenolepis Infection]
    E. coli Infection [Escherichia coli Infection]
    Ear Infection [Otitis Media]
    Early Hearing Detection and Intervention (EHDI) - see Hearing,
    Early Detection & Intervention
    Eastern Equine Encephalitis (EEE)
    Ebola Virus Disease (EVD)
    EBV Infection (Epstein-Barr Virus Infection)
    Echinococcosis
    EEE (Eastern Equine Encephalitis)
    EHDI (Early Hearing Detection and Intervention)
    Ehrlichiosis, Human
    Elephantiasis - see Lymphatic Filariasis
    Emerging Infectious Diseases
    Entamoeba histolytica infection - see Amebiasis, Intestinal
    Enteric Diseases from Animals - see Gastrointestinal Diseases from
    Animals
    Enterobius vermicularis Infection - see Pinworm Infection
    Enterovirus D68
    Enterovirus Infections (Non-Polio) - see Non-Polio Enterovirus
    Infections
    Epidemic Typhus - see Typhus Fevers
    Epilepsy
    Epstein-Barr Virus Infection (EBV Infection)
    Ergonomic and Musculoskeletal Disorders
    Escherichia coli Infection - see E. coli Infection
    Esophageal Candidiasis - see Thrush
    EVD (Ebola Virus Disease)
    EV-D68 - see Enterovirus D68
    Exserohilum rostratum (Other Pathogenic Fungi)
    Extensively Drug-Resistant TB (XDR TB)
    Extreme Cold [Hypothermia]
    Extreme Heat [Hyperthermia]
    Falls from Elevation
    Falls, Older Adults
    Fasciitis, Necrotizing
    Fasciola Infection [Fascioliasis]
    Fascioliasis - see Fasciola Infection
    Fasciolopsiasis - see Fasciolopsis Infection
    Fasciolopsis Infection [Fasciolopsiasis]
    Fetal Alcohol Syndrome
    FETP - see Field Epidemiology Training Program
    FETP (Field Epidemiology Training Program)
    Fibromyalgia
    Fifth Disease [Parvovirus B19 Infection]
    Filariasis, Lymphatic
    Fireworks Injuries
    Flu
    Folliculitis
    Foodborne Illness
    Food-Related Diseases
    Fragile X Syndrome (FXS)
    Francisella tularensis Infection - see Tularemia
    Fungal diseases [Mycotic diseases]
    Fungal Keratitis
    Fungal Meningitis
    Fungal Pneumonia - see Valley Fever
    FXS (Fragile X Syndrome)
    GAE (Granulomatous amebic encephalitis)
    GAS (Group A Strep Infection)
    Gastrointestinal Diseases from Animals [Zoonotic enteric diseases]
    GBS (Group B Strep Infection)
    GBS and Menactra Meningococcal Vaccine - see Guillain-Barré
    Syndrome and Menactra Meningococcal Vaccine
    GDDER (Global Disease Detection and Emergency Response)
    Genetics and Autism - see Autism and Genetics
    Genetics and Colorectal Cancer - see Colorectal Cancer and Genetics
    Genetics and Heart Disease - see Heart Disease and Genetics
    Genetics and Mental Health - see Mental Health and Genetics
    Genetics and Obesity - see Obesity and Genetics
    Genetics and Skin Cancer - see Skin Cancer and Genetics
    Genetics and Stroke - see Stroke and Genetics
    Genital Candidiasis (VVC) [Vulvovaginal Candidiasis]
    Genital Herpes [Herpes Simplex Virus Infection]
    Genital Warts - see Human Papillomavirus Infection
    German Measles (Rubella Virus)
    Giardia Infection [Giardiasis]
    Giardiasis - see Giardia Infection
    Glanders [Burkholderia mallei]
    Gnathostoma Infection - see Gnathostomiasis
    Gnathostomiasis [Gnathostoma Infection]
    Gonorrhea [Neisseria gonorrhoeae Infection]
    Gout
    Granulomatous amebic encephalitis (GAE) - see Balamuthia Infection
    Group A Strep Infection (GAS) [Group A Streptococcal Infection]
    Group A Streptococcal Infection - see Group A Strep Infection
    Group B Strep Infection (GBS) [Group B Streptococcal Infection]
    Group B Streptococcal Infection - see Group B Strep Infection
    Guillain-Barré Syndrome and Menactra Meningococcal Vaccine
    Guinea Worm Disease [Dracunculiasis]
    Gynecologic Cancers
    H1N1 Flu
    H3N2v influenza
    H5N1 - see Avian Influenza
    Haemophilus influenzae Serotype b - see Hib Infection
    Haemophilus influenzae Infection (including Hib Infection)
    Hand, Foot, and Mouth Disease (HFMD)
    Hansen's Disease
    Hantavirus Pulmonary Syndrome (HPS)
    Hazardous Drug Exposures in Healthcare
    Head Lice [Pediculus humanus capitis]
    Health Disparities in Cancer
    Health Disparities in HIV/AIDS, Viral Hepatitis, STDs, and TB
    Health Security - see Global Health Security
    Healthcare Associated Infections
    Healthy Pets, Healthy People - see Animal-Related Diseases
    Hearing Loss in Children
    Heart Disease [Cardiovascular Health]
    Heart Disease and Genetics
    Heat Stress
    Hemochromatosis
    Hemoglobinopathies
    Hemophilia
    Hemophilia Treatment Centers (HTC)
    Hemorrhagic Fevers, Viral - see Viral Hemorrhagic Fevers
    Hendra Virus Disease (HeV Infection)
    Hepatitis A Vaccination
    Hepatitis B Vaccination
    Hepatitis, Viral - see Viral Hepatitis
    Hereditary Bleeding Disorders - see Hemophilia
    Herpes B virus - see B virus Infection
    Herpes Simplex Virus Infection - see Genital Herpes
    Herpes Zoster - see Shingles
    Herpes Zoster Vaccination - see Shingles Vaccination
    Herpes, Genital - see Genital Herpes
    Herpesvirus B - see B virus Infection
    Herpesvirus simiae - see B virus Infection
    Heterophyes Infection [Heterophyiasis]
    Heterophyiasis - see Heterophyes Infection
    HeV Infection (Hendra Virus Disease)
    HFMD (Hand, Foot, and Mouth Disease)
    Hib Infection [Haemophilus influenzae Serotype b]
    Hib Vaccine (Haemophilus influenzae Serotype b Vaccination)
    High Blood Pressure
    Histoplasma capsulatum Infection [Histoplasmosis]
    Histoplasmosis - see Histoplasma capsulatum Infection
    Histoplasmosis [Histoplasma capsulatum Infection]
    HIV/AIDS
    HIV/AIDS and STDs
    Hookworm, Human [Ancylostoma duodenale Infection,
    Necator americanus Infection] see Human Hookworm
    Hookworm, Zoonotic - see Zoonotic Hookworm
    Horses, Infections from
    Hot Tub Rash [Pseudomonas dermatitis Infection]
    HPIV (Human Parainfluenza Viruses)
    HPS (Hantavirus Pulmonary Syndrome)
    HPV Infection (Human Papillomavirus Infection)
    HPV Vaccination (Human Papillomavirus Vaccination)
    HPV-Associated Cancers
    HTC (Hemophilia Treatment Centers)
    Human Ehrlichiosis - see Ehrlichiosis, Human
    Human Hookworm [Ancylostoma duodenale Infection,
    Necator americanus Infection]
    Human Immunodeficiency Virus - see HIV/AIDS
    Human Papillomavirus Infection (HPV Infection)
    Human Papillomavirus Vaccination (HPV Vaccination)
    Human Parainfluenza Viruses (HPIV)
    Hymenolepis Infection - see Dwarf Tapeworm
    Hypertension - see High Blood Pressure
    Hyperthermia - see Extreme Heat
    Hypothermia - see Extreme Cold
    IBD (Inflammatory Bowel Disease)
    IMMPaCt (International Micronutrient Malnutrition Prevention and
    Control Program) see Micronutrient Malnutrition
    Impetigo - see Group A Strep Infection
    including Hib Infection (Haemophilus influenzae Infection)
    Infectious Mononucleosis - see Epstein-Barr Virus Infection
    Infertility
    Inflammatory Bowel Disease (IBD)
    Influenza
    Influenza and Cancer - see Cancer and Flu
    Influenza in Pigs - see Swine Influenza
    Influenza Vaccination
    Influenza, Avian - see Avian Influenza
    Influenza, Pandemic - see Pandemic Flu
    Injury, Healthy Swimming and Recreational Water
    International Micronutrient Malnutrition Prevention & Control
    Program (IMMPaCt) - see Micronutrient Malnutrition
    Intestinal Amebae Infection, Nonpathogenic - see Nonpathogenic
    (Harmless) Intestinal Protozoa
    Invasive Candidiasis
    Iron Deficiency - see Anemia
    Iron Overload [Hemochromatosis] - see Hemochromatosis
    Iron Storage Disease
    Isospora Infection [Isosporiasis] - see Cystoisospora Infection
    Japanese Encephalitis (JE)
    Jaundice - see Newborn Jaundice
    JE (Japanese Encephalitis)
    K. pneumoniae (Klebsiella pneumoniae)
    Kala-Azar - see Leishmania Infection
    Kawasaki Syndrome (KS)
    Keratitis, Fungal - see Fungal Keratitis
    Kernicterus - see Newborn Jaundice
    KFD (Kyasanur Forest disease)
    Kidney Disease (CKD)
    Klebsiella pneumoniae (K. pneumoniae)
    KS (Kawasaki Syndrome)
    Kyasanur Forest disease (KFD)
    La Crosse Encephalitis (LAC)
    La Crosse Encephalitis virus (LACV) - see La Crosse Encephalitis
    LAC (La Crosse Encephalitis)
    LACV (La Crosse Encephalitis virus)
    Lassa Fever
    Latex Allergies
    LCM (Lymphocytic Choriomeningitis)
    Lead Poisoning
    Legionellosis - see Legionnaires' Disease
    Legionnaires' Disease [Legionellosis]
    Leishmania Infection [Leishmaniasis]
    Leishmaniasis - see Leishmania Infection
    Leprosy - see Hansen's Disease
    Leptospira Infection [Leptospirosis]
    Leptospirosis - see Leptospira Infection
    Lice
    Listeria Infection [Listeriosis]
    Listeriosis - see Listeria Infection
    Liver Disease and Hepatitis - see Viral Hepatitis
    Loa loa Infection - see Loiasis
    Lockjaw - see Tetanus Disease
    Lockjaw Vaccination - see Tetanus (Lockjaw) Vaccination
    Loiasis [Loa loa Infection]
    Lou Gehrig's Disease - see ALS
    LUHF (Lujo Hemorrhagic Fever)
    Lujo Hemorrhagic Fever (LUHF)
    Lung Cancer
    Lupus (SLE) [Systemic lupus erythematosus]
    Lyme Disease [Borrelia burgdorferi Infection]
    Lymphatic Filariasis
    Lymphedema - see Lymphatic Filariasis
    Lymphocytic Choriomeningitis (LCM)
    MAC (Mycobacterium avium Complex)
    Mad Cow Disease (BSE) - see Bovine Spongiform Encephalopathy
    Malaria
    Marburg Hemorrhagic Fever
    Marine Toxins
    MD (Muscular Dystrophy)
    MDR TB (Multidrug-Resistant TB)
    Measles
    Melioidosis [Burkholderia pseudomallei Infection]
    Meningitis
    Meningococcal Disease
    Meningococcal Vaccination
    Men's Health
    Mental Health
    Mental Health and Genetics
    Mental Retardation
    MERS-CoV (Middle East Respiratory Syndrome Coronavirus)
    Methicillin Resistant Staphylococcus aureus - see MRSA
    Micronutrient Malnutrition
    Microsporidia Infection
    Middle East Respiratory Syndrome Coronavirus (MERS-CoV)
    MMR Vaccination
    Molluscum Contagiosum
    Monkey B virus - see B virus Infection
    Monkeypox
    Monkeypox Vaccination
    Mononucleosis, Infectious - see Epstein-Barr Virus Infection
    Motor Vehicle Injuries
    Mouse and Rat Control - see Rodents, Diseases from
    MRSA [Methicillin Resistant Staphylococcus aureus]
    Mucormycosis
    Mucus - see Cold, Common
    Multidrug-Resistant TB (MDR TB)
    Multiple organ dysfunction syndrome - see Sepsis
    Mumps
    Muscular Dystrophy (MD)
    Musculoskeletal Disorders - see Ergonomic and Musculoskeletal
    Disorders
    Mycobacterium abscessus Infection
    Mycobacterium avium Complex (MAC)
    Mycobacterium tuberculosis Infection - see Tuberculosis
    Mycoplasma pneumoniae Infection
    Mycotic diseases - see Fungal diseases
    Myelomeningocele - see Spina Bifida
    Myiasis
    Naegleria Infection [Primary Amebic Meningoencephalitis (PAM)]
    Nairovirus Infection - see Crimean-Congo hemorrhagic fever
    National Amyotrophic Lateral Sclerosis (ALS) Registry - see ALS
    Necrotizing Fasciitis - see Group A Strep Infection
    Neglected Tropical Diseases (NTD)
    Neisseria gonorrhoeae Infection - see Gonorrhea
    Neurocysticercosis - see Cysticercosis
    Newborn Hearing - see Hearing, Early Detection & Intervention
    Newborn Jaundice [Kernicterus]
    Nocardia asteroides Infection - see Nocardiosis
    Nocardiosis [Nocardia asteroides Infection]
    Nonpathogenic (Harmless) Intestinal Protozoa
    Non-Polio Enterovirus Infections
    Norovirus Infection
    Norwalk-like Viruses (NLV) - see Norovirus Infection
    NTD (Neglected Tropical Diseases)
    OA (Osteoarthritis)
    Obesity and Genetics
    Obesity and Overweight
    Obesity and Overweight, Childhood - see Childhood Overweight
    and Obesity
    Occupational Cancers
    Occupational Skin Conditions - see Skin Conditions, Occupational
    Occupational Stress - see Stress, Occupational
    OHF (Omsk hemorrhagic fever)
    Omsk hemorrhagic fever (OHF)
    Onchocerciasis - see River Blindness
    Opisthorchis Infection
    Oral Cancer
    Orf Virus Infection - see Sore Mouth Infection
    Oropharyngeal Candidiasis - see Thrush
    Oroya fever - see Carrión's disease
    Osteoarthritis (OA)
    Osteoporosis - see Bone Health
    Otitis Media - see Ear Infection
    Outbreaks
    Ovarian and Breast Cancer and Family Health History - see Breast
    and Ovarian Cancer and Family Health History
    Ovarian Cancer
    PAD (Peripheral Arterial Disease)
    Pandemic Flu
    Paragonimiasis - see Paragonimus Infection
    Paragonimus Infection [Paragonimiasis]
    Parainfluenza - see Human Parainfluenza Viruses
    Parasitic Diseases
    Parvovirus B19 Infection - see Fifth Disease
    PCP (Pneumocystis pneumonia)
    PCV (Pneumococcal Conjugate Vaccine)
    PE (Pulmonary Embolism)
    Pedestrian Injury
    Pediculus humanus capitis - see Head Lice
    Pediculus humanus corporis - see Body Lice
    Pelvic Inflammatory Disease (PID)
    Peripheral Arterial Disease (PAD)
    Peripheral Arterial Insufficiency - see Peripheral Arterial Disease
    Peripheral Arterial Occlusive Disease - see Peripheral Arterial Disease
    Peripheral Vascular Disease - see Peripheral Arterial Disease
    Pertussis (Whooping Cough)
    Pertussis (Whooping Cough) Vaccination
    Pet-Related Diseases - see Animal-Related Diseases
    Phthiriasis - see Pubic Lice
    PID (Pelvic Inflammatory Disease)
    Pigs, Influenza in - see Swine Influenza
    Pink Eye [Conjunctivitis]
    Pinworm Infection [Enterobius vermicularis Infection]
    Plague [Yersinia pestis Infection]
    Pneumococcal Conjugate Vaccine (PCV)
    Pneumococcal Disease
    Pneumococcal Polysaccharide Vaccine (PPV)
    Pneumoconioses, Coal Workers' - see Black Lung
    Pneumocystis carinii Pneumonia (PCP) Infection - see Pneumocystis
    pneumonia
    Pneumocystis jirovecii pneumonia (previously Pneumocystis carinii) -
    see Pneumocystis pneumonia
    Pneumocystis pneumonia (PCP) [Pneumocystis jirovecii pneumonia
    (previously Pneumocystis carinii)]
    Pneumonia
    Polio Infection [Poliomyelitis Infection]
    Polio Vaccination [Poliomyelitis Vaccination]
    Poliomyelitis Infection - see Polio Infection
    Poliomyelitis Vaccination - see Polio Vaccination
    Pontiac Fever - see Legionnaires' Disease
    Powassan (POW) virus
    Poxvirus Infections
    PPV (Pneumococcal Polysaccharide Vaccine)
    Primary Amebic Meningoencephalitis (PAM) - see Naegleria Infection
    Prion Diseases (TSEs) [Transmissible spongiform encephalopathies]
    Prostate Cancer
    Pseudomonas dermatitis Infection - see Hot Tub Rash
    Psittacosis
    Psoriasis
    Pubic Lice [Phthiriasis]
    Pulmonary Embolism (PE) - see Deep Vein Thrombosis
    Pulmonary Hypertension
    Q Fever [Coxiella burnetii Infection]
    RA (Rheumatoid Arthritis)
    Rabies
    Raccoon Roundworm Infection [Baylisascaris Infection]
    Rat-Bite Fever (RBF) [Streptobacillus moniliformis Infection]
    RBF (Rat-Bite Fever)
    Recreational Water Illness (RWI)
    Reptiles, Infections from
    Respiratory Syncytial Virus Infection (RSV)
    Rheumatoid Arthritis (RA)
    Rickettsia rickettsii Infection - see Rocky Mountain Spotted Fever
    Rickettsia, Spotted Fever Group - see Spotted Fever Group Rickettsia
    Rickettsial Diseases
    Rift Valley Fever (RVF)
    Ringworm [Dermatophyte Infection]
    Ringworm [Dermatophytes]
    Ringworm in Animals
    River Blindness [Onchocerciasis]
    RMSF (Rocky Mountain Spotted Fever)
    Rocky Mountain Spotted Fever (RMSF) [Rickettsia rickettsia
    Infection]
    Rodent Control - see Rodents, Diseases from
    Rodents - see Rat-Bite Fever
    Rodents, Diseases from
    Rotavirus Infection
    RSV (Respiratory Syncytial Virus Infection)
    Rubella (German Measles) Vaccination
    Rubeola - see Measles
    Runny Nose - see Cold, Common
    RVF (Rift Valley Fever)
    RWI (Recreational Water Illness)
    Salmonella typhi Infection - see Typhoid Fever
    Salmonella Infection [Salmonellosis]
    Salmonellosis - see Salmonella Infection
    Sappinia diploidea and Sappinia pedata - see Sappinia Infection
    Sappinia Infection [Sappinia diploidea and Sappinia pedata]
    SARS [Severe Acute Respiratory Syndrome]
    Scabies
    Scarlet Fever
    Schistosoma Infection - see Schistosomiasis
    Schistosomiasis [Schistosoma Infection]
    Seasonal Flu
    Sepsis [Septicemia]
    Septic shock - see Sepsis
    Septicemia - see Sepsis
    Severe Acute Respiratory Syndrome - see SARS
    Sexually Transmitted Disease Surveillance Reports
    Sexually Transmitted Diseases (STDs)
    SFGR (Spotted Fever Group Rickettsia)
    Shigella Infection [Shigellosis]
    Shigellosis - see Shigella Infection
    Shingles [Varicella Zoster Virus (VZV)]
    Shingles Vaccination
    Sickle Cell Disease
    SIDS (Sudden Infant Death Syndrome)
    Sinus Infection [Sinusitus]
    Sinusitus - see Sinus Infection
    Skin Cancer
    Skin Cancer and Genetics
    Skin Conditions, Occupational
    SLE (Lupus)
    Sleep and Sleep Disorders
    Sleeping Sickness [African Trypanosomiasis]
    Smallpox [Variola Major and Variola Minor]
    Smallpox Vaccination
    Smoking and Tobacco Use
    Sodium - see Salt
    Soil Transmitted Helminths
    Sore Mouth Infection [Orf Virus Infection]
    Sore Throat
    Southern Tick-Associated Rash Illness (STARI)
    Spina Bifida [Myelomeningocele]
    Spirillum minus Infection - see Rat-Bite Fever
    Sporothrix schenckii infection - see Sporotrichosis
    Sporotrichosis
    Sporotrichosis [Sporothrix schenckii infection]
    Spotted Fever Group Rickettsia (SFGR)
    Staph - see Staphylococcus aureus Infection
    Staphylococcus aureus Infection
    STARI (Southern Tick-Associated Rash Illness)
    STDs (Sexually Transmitted Diseases)
    STDs and HIV/AIDS - see HIV/AIDS and STDs
    Strep Infection, Group A - see Group A Strep Infection
    Strep Infection, Group B - see Group B Strep Infection
    Strep Throat - see Sore Throat
    Streptobacillus moniliformis Infection - see Rat-Bite Fever
    Streptococcus pneumoniae Infection
    Stress, Occupational
    Stroke
    Stroke and Genetics
    Strongyloidiasis - see Strongyloides Infection [Strongyloidiasis]
    Strongyloidiasis - see Strongyloidiasis - see Strongyloides Infection
    Sudden Infant Death Syndrome (SIDS)
    surgical site infection (SSI)
    Surveillance Reports, Sexually Transmitted Disease - see Sexually
    Transmitted Disease Surveillance Reports
    Swimmer's Itch [Cercarial Dermatitis]
    Swimming-related Illness - see Recreational Water Illness
    Swine Influenza
    Symptom Relief for Upper Respiratory Infections
    Syphilis [Treponema pallidum Infection]
    Systemic lupus erythematosus - see Lupus
    Taenia Infection - see Tapeworm Infection
    Tapeworm Infection [Taenia Infection]
    Tapeworm, Dog and Cat Flea [Dipylidium Infection]
    TB (Tuberculosis)
    TB (Tuberculosis) Vaccination
    TB and HIV Coinfection
    TBI (Traumatic Brain Injury)
    Testicular Cancer
    Tetanus (Lockjaw) Infection
    Tetanus (Lockjaw) Vaccination
    Tetanus Disease [Clostridium tetani Infection]
    Thalassemia - see Cooleys Anemia
    Thoracic Aortic Aneurysm - see Aortic Aneurysm
    Throat, Sore - see Sore Throat
    Throat, Strep - see Sore Throat
    Thrombophilia - see Clotting Disorders
    Thrombosis - see Clotting Disorders
    Thrush [Oropharyngeal Candidiasis]
    Tickborne Diseases - see Ticks
    Ticks
    Tinea - see Ringworm
    Tobacco Use, Smoking and - see Smoking and Tobacco Use
    Tourette Syndrome (TS)
    Toxocara Infection - see Toxocariasis
    Toxocariasis [Toxocara Infection]
    Toxoplasma Infection - see Toxoplasmosis
    Toxoplasmosis [Toxoplasma Infection]
    Trachoma Infection
    Transmissible spongiform encephalopathies - see Prion Diseases
    Traumatic Brain Injury (TBI)
    Traumatic Occupational Injuries
    Trench fever [Bartonella quintana Infection]
    Treponema pallidum Infection - see Syphilis
    Trichinellosis (Trichinosis)
    Trichomonas Infection - see Trichomoniasis
    Trichomoniasis [Trichomonas Infection]
    Trichuriasis - see Whipworm Infection
    Trisomy 21 - see Down Syndrome
    Trypanosoma cruzi Infection - see Chagas Disease
    Trypanosomiasis, African - see Sleeping Sickness
    TS (Tourette Syndrome)
    TSEs (Prion Diseases)
    Tuberculosis (TB) [Mycobacterium tuberculosis Infection]
    Tuberculosis (TB) Vaccination
    Tuberculosis and HIV Coinfection - see TB and HIV Coinfection
    Tuberculosis Skin Test - see TB Testing & Diagnosis
    Tuberculosis Training - see TB Education and Training Network
    Tuberculosis Vaccine (BCG)
    Tularemia [Francisella tularensis Infection]
    Typhoid Fever [Salmonella typhi Infection]
    Typhoid Fever Vaccination
    Typhus Fevers
    Ulcerative Colitis - see Inflammatory Bowel Disease
    Undulant Fever - see Brucella Infection
    Unexplained Respiratory Disease Outbreaks (URDO)
    Upper Respiratory Infection Symptom Relief - see Symptom Relief
    for Upper Respiratory Infections
    URDO (Unexplained Respiratory Disease Outbreaks)
    Uterine Cancer
    Vaginal and Vulvar Cancers
    Vaginal Candidiasis - see Genital Candidiasis
    Valley Fever [Coccidioidomycosis]
    Vancomycin-Intermediate/Resistant Staphylococcus aureus
    Infections [VISA/VRSA]
    Vancomycin-resistant Enterococci Infection (VRE)
    Variant Creutzfeldt-Jakob Disease (vCJD)
    Variant Viruses - see Influenza
    Varicella Disease - see Chickenpox
    Varicella Zoster Virus (VZV) - see Shingles
    Varicella-Zoster Virus Infection
    Variola Major and Variola Minor - see Smallpox
    vCJD (Variant Creutzfeldt-Jakob Disease)
    verruga peruana - see Carrión's disease
    VHF (Viral Hemorrhagic Fevers)
    Vibrio cholerae Infection - see Cholera
    Vibrio Illness [Vibriosis]
    Vibriosis - see Vibrio Illness
    Viral Hemorrhagic Fevers (VHF)
    Viral Hepatitis
    Viral Meningitis [Aseptic Meningitis]
    VISA/VRSA - see Vancomycin-Intermediate/Resistant
    Staphylococcus aureus Infections
    Vision Impairment
    VRE (Vancomycin-resistant Enterococci Infection)
    Vulvovaginal Candidiasis - see Genital Candidiasis
    VVC (Genital Candidiasis)
    VZV (Varicella Zoster Virus) - see Shingles
    Water-Related Diseases
    Weight, Healthy - see Healthy Weight
    West Nile Virus Infection (WNV Infection)
    Whipworm Infection [Trichuriasis]
    Whitmore's Disease - see Melioidosis
    Whooping Cough - see Pertussis (Whooping Cough)
    Wildlife, Infections from
    WNV Infection (West Nile Virus Infection)
    Women's Bleeding Disorders
    XDR TB (Extensively Drug-Resistant TB)
    Xenotropic Murine Leukemia Virus-related Virus Infection - see
    XMRV Infection
    XMRV Infection [Xenotropic Murine Leukemia Virus-related
    Virus Infection]
    Yeast Infection - see Genital Candidiasis
    Yellow Fever
    Yellow Fever Vaccination
    Yersinia enterocolitica Infection - see Yersiniosis
    Yersinia pestis Infection - see Plague
    Yersiniosis [Yersinia enterocolitica Infection]
    Zoonotic Diseases from Animals - see Animal-Related Diseases
    Zoonotic enteric diseases - see Gastrointestinal Diseases from Animals
    Zoonotic Hookworm
    Zoster - see Shingles
    Zygomycosis - see Mucormycosis
  • III. System and Method to Control the Delivery of Oral Medications
  • Various embodiments will be described hereinafter with reference to the accompanying drawings. These embodiments are illustrated and described by example only and are not intended to be limiting. Alternate embodiments may be devised without departing from the spirit or the scope of the invention. Additionally, well-known elements of exemplary embodiments of the invention will not be described in detail or will be omitted so as not to obscure the relevant details of the invention. Further, to facilitate an understanding of the description discussion of several terms used herein follows.
  • The word “exemplary” is used herein to mean “serving as an example, instance, or illustration”. Any embodiment described herein as “exemplary” or “example” is not necessarily to be construed as preferred or advantageous over other embodiments. Likewise, the term “embodiments of the invention” does not require that all embodiments of the invention include the discussed feature, advantage or mode of operation.
  • Further, many embodiments are described in terms of sequences of actions to be performed by, for example, elements of a computing device. It will be recognized that various actions described herein can be performed by specific circuits (e.g., application specific integrated circuits (ASICs)), by program instructions being executed by one or more processors, or by a combination of both. Additionally, these sequences of actions described herein can be considered to be embodied entirely within any form of computer readable storage medium having stored therein a corresponding set of computer instructions that upon execution would cause an associated processor to perform the functionality described herein. Thus, the various aspects of the invention may be embodied in a number of different forms, all of which have been contemplated to be within the scope of the claimed subject matter. In addition, for each of the embodiments described herein, the corresponding form of any such embodiments may be described herein as, for example, “logic configured to” perform the described action.
  • FIG. 1 illustrates an exemplary embodiment of the present invention, an integrated drug dispensing and disease management system composed of a Drug Specific App 10 which contains a Drug Specific Dispensing Algorithm 15 resident on an Interface Device (Smart Phone, computer Tablet, portable or desktop computer, standalone drug dispenser, etc. with Internet communications capabilities) 20 used to control dispensing by a (single or multidrug) Drug Dispenser 30; an Integrated Support Center 40; a Patient 50; a Prescriber 60; and the Patient's Electronic Medical Record 70.
  • FIG. 2 is an exemplary embodiment depicting a Drug Specific Dispensing App 80 which resides on an Interface Device 20 and controls drug dispensing. When the Patient 50 is prescribed a Drug, the Patient 50 is trained on the operation of the Drug Specific Dispensing App 80 and the related Drug Dispenser 30 using the Apps training interface.
  • In this embodiment of the invention, the Drug Specific App 80 is comprised of the following software modules: (i) Biometric Authentication 80 a, (ii) Prescription 80 b module which can be programmed remotely by the Integrated Support Center 40, (iii) Patient Reminder 80 c, (iv) Interface Device 80 d, (v) Patient Self-Assessment 80 e module which is unique for each drug, (vi) Digital Capture (APIs) 80 f, (vii) the Drug Specific Dispensing Algorithm 80 g which is unique for each drug, (viii) Dispensing Communication and Reporting 80 h, (ix) the Integrated Support Center 80 i, (x) the Patient Reporting 80 j, and (xi) the App and Dispensing Unit Operation Training Interface 80 k.
  • The following are exemplary descriptions of the FIG. 2 embodiments of the invention:
  • Biometric Authentication module 80 a encompasses the utilization of a biometric authentication screen and/or digital interface which allows the patient, upon authentication, to automatically move to the Patient Self- Assessment screens 100, 102, 104 if: (i) the authentication routine recognizes the Drug Dispenser's 30 serial number to be one that was registered to the Patient 50, (ii) digitally Handshake with the Drug Specific App 10 and (iii) the Biometric Authentication 80 a recognizes the Patient 50. If the Biometric Authentication 80 a does not recognize the Patient 50, it asks the Patient 50 to try again. After a given number of tries, it alerts the patient to talk with the Integrated Support Center 40 and alerts the Integrated Support Center 40 of the failed attempts and lists the Patient 50 for a follow-up call if the drug has not been properly dispensed within a drug specific timeframe. If the App 50 does not recognize the Drug Dispenser 30, the patient gets an alert screen explaining why it does not recognize the dispenser, this may include but is not limited to: (i) unable to locate the Drug Dispenser 30, (ii) the Drug Dispenser 30 does not have the right serial number, etc. Simultaneously, if the App 10 senses that the Drug Dispenser does not have the right serial number, it will send a message to the Integrated Support Center 40 indicating the serial number of the recognized Drug Dispenser for follow-up action by the Integrated Support Center 40. One alternative for the Integrated Support Center 40 is to lock the App screen to only give the Patient 50 the choice of calling the Integrated Support Center 40 to resolve his dispensing issue.
  • The Prescription module 80 b, which is unique to the drug, encompasses the ability of the Prescriber 60, other authorized healthcare professionals, or the Integrated Support Center 40 to input the prescribing information into the Drug Specific App 10. After loading the Drug Specific App 10 onto the Interface Device 20, the person entering the prescription information begins by entering the drugs Brand and/or generic name, strength/dosage, NCD number, Batch Number, any pertinent required contact information in case of an overdose or emergency, and the drug's expiration date. This input can be done manually and/or via a barcode scan of the Individualized Drug Cassette 170. The prescribing information defines the dosing strength and administration schedule (e.g, q.d., b.i.d., t.i.d., q.i.d., q.h.s., −X a day, −X per week, −X per month, q.4h, q.6h, q.o.d., a.c., p.c., prn, etc.). The prn dosing, and/or for example the patient self-analgesia dosing, can be designated to allow the Patient 50 to self-medicate using multiple smaller doses to a maximum cumulative dose over a specified period of time. Once the maximum does is dispensed, the Drug Dispenser is locked by the Drug Specific App 10 until the next dosing period begins and the patient enters the requisite information to enable the Drug Specific App 10 to signal the Drug Dispenser to dispense.
  • The Patient Reminder module 80 c encompasses the ability of the Drug Specific App 10 to alert the Patient 50 using different methodologies including but not limited to: (i) initiating a phone call, (ii) buzzing the device, (iii) sending an email message, (iv) sending a text message, and/or (v) having the Integrated Support Center 40 call the Patient 50, etc.
  • When the phone call is initiated, the Drug Specific App 10 is shown on the Smart Phone's screen. When the phone is turned on or unlocked, the screen automatically moves to the Biometric Authentication 90 screen. If the Drug Specific App 10 is clicked on a Smart Phone, it opens to the Biometric Authentications 90 screen.
  • The Interface Device module 80 d encompasses many functions: (i) home for the Drug Specific App 10, (ii) enables the Drug Specific App 10 to utilize the Interface Device features to facilitate the Drug Specific App's interface with the Patient 50, (iii) uses the Interface Device's 20 Wi-Fi communications capability to interface with the Drug Dispenser 30 and its Internet communications capability to interface with the Integrated Support Center 40, (iv) uses the phone to call the Integrated Support Center 40, and utilizes the Interface Device's 20 memory to store the prescription, dispensing history, and the Patient Self-Assessment (see illustrative examples in FIG. 4) and digital (see representative examples under FIG. 5) physiological, psychological, lifestyle, currently taken medications, and environmental data.
  • The Patient 50 is, for example, able to utilize the Interface Device's 20 navigation capabilities to move between screens and to correct prior inputs before exiting by selecting the dispense or exit buttons.
  • Utilizes the Interface Device's 20 GPS device to capture the location when the medication is dispensed.
  • Patient Self-Assessment module 80 e is specific for each drug based upon, for example, the drug's side effects, potential drug interactions, implications of under and/or overdosing, efficacy measures, dosing schedule, drug strength, single or multidrug regimen, effects of weight gain, aging, development of comorbidities, etc. Certain Patient Self- Assessment 100, 102, 104 screens will, for example, incorporate known self-assessment scales or will incorporate self-assessment screens specifically developed for the specific drug. The screens may also be those which are designed to capture Patient specific information required by regulatory agencies for the subsequent approval of the drug and/or for post marketing studies.
  • The Digital Capture (APIs) module 80 f encompasses, as an exemplary, digital information that is integrated via the Drug Specific App 10 via Digital Capture from, as examples, a wearable monitoring device 110, a digital scale 112, a third-party monitoring App on a smart phone 114, a hand held diagnostic device 116, a lifestyle monitor 117, a digitalized home diagnostic or self-diagnostic 118, a swallowed tracking and/or diagnostic aid, a drug tracking chip, radio frequency identification device (RFID), or care giver or parent patient assessments and/or journal entries, etc.
  • The Drug Specific Dispensing Algorithm module 80 g encompasses, as an example, the Product Expiration 122 date, Properly Stored 123 information (for example, temperature, moisture, etc.), one or more Patient Self- Assessment 125, 126 and/or one or more Digitally Captured 127 values, the Dispensing Algorithm 128, the Dispense 129 command screen and interface with the Drug Dispenser 30, and patient feedback and instruction screens 130, 132, 134, 136, 138, 140, 142, 144, 146, 148, 150, 152, etc.
  • The Dispensing Communications and Reporting 80 h module encompasses, for example, the interface between: (i) the Drug Specific App 10 and the Drug Dispenser 30 via the Interface Device 20; (ii) the interfaces between the Drug Specific App 10 and any proprietary or third-party digital devices, data aggregation devices, computer databases, diagnostic devices, and medication tracking devices, etc., for example, those digital devices listed under FIG. 5, e.g., 110, 112, 114, 116, 117, 118; (iii) the interface between the Drug Specific App and the computer servers and the respective databases that store information captured by the Drug Specific App 10 and data and reports created by the Integrated Support Center 40 and accessed by the Drug Specific App 10; the interface between the Integrated Support Center 40 and the Drug Specific App 10 utilized to change the prescription on the Drug Specific App 10 as well as to update the App software as required, etc.
  • The Integrated Support Center 80 i module encompasses, for example, (i) securely handshaking/connecting the Drug Specific App 10 to the Integrated Support Center 40, (ii) sending to and receiving alerts from the Integrated Support Center 40, (iii) enabling the Integrated Support Center 40 to lock or unlock the Drug Dispenser 30, (iv) alert the Integrated Support Center 40 of unusual attempts to open the Drug Dispenser 30, (v) the ability of the Integrated Support Center 40 to remotely update the Drug Specific App software, and (vi) enables the Drug Specific App 10 to access patient reports, charts, and graphs, (vii) enables the patient to require a refill prescription be sent to his/her pharmacy for refill, etc.
  • The Patient Reporting 80 j module encompasses, as an example: (i) an ability by the Patient 50 to request certain reports, e.g., the last time the Patient 50 took the medication, prescription information details, drug details (brand and generics names, batch number, expiration date, doses remaining, reorder information, drug interactions, typical side effects, etc.; (ii) graphs and charts created by the Drug Specific App 10 based upon Interface Device 20 stored information; (iii) graphs, charts and/or reports downloaded from the Integrated Support Center's servers, etc.
  • The App and Dispensing Unit Operation Training Module 80 k encompasses, as an example, (i) a hot link to a video library resident on the Integrated Support Center's servers, You Tube, and/or other consumer video services covering all aspects of utilizing the Drug Specific App 10, using and troubleshooting the Drug Dispenser 30, (ii) a step by step tutorial resident on the Interface Device 20, (iii) a hot linked “help” button on each respective screen allowing the Patient 50 to bring up usage instructions for the respective screen without interrupting the sequence of entering the required prescription information or selecting a particular command, etc.
  • FIG. 3 The exemplary embodiment of the Biometric Authentication 90 interface encompasses a system that is compliant with the Health Insurance Portability and Accountability Act (HIPAA), which sets the standard for protecting sensitive patient data. This means that all the required physical, network, and process security measures are in place and followed and incorporated herein by reference.
  • FIG. 4 The exemplary embodiment of the Patient Self- Reporting Screens 100, 102, 104 encompass, for example, an abdominal pain self-reporting scale adapted from Wong Baker Faces 100; the stool consistency utilizes the Bristol Stool Scale, a well-accepted stool measure 102; and the current abdominal discomfort scale was developed by MMC International from the Defense and Veterans Pain Rating Scale 104. These are examples of patient self-reporting screens that can be utilized in the embodiment as an input to the Drug Specific Dispensing Algorithm 15 to decide whether or not to dispense. The scales can be created, adapted, or integrated to capture the desired patient self-reported information. This can be, for example, for clinical trials, post marketing surveillance, and/or for incorporation into the Drug Specific Dispensing Algorithm 15.
  • FIG. 5 The exemplary embodiment of the Digitally Captured information 110, 112, 114, 116, 117, 118 is illustrative for the types of digital information which can be collected and integrated into the Decision Tree/logic in the respective Drug Specific Dispensing Algorithms 15. The availability of disease specific Apps and related disease or condition specific digitalized health information is rapidly emerging, making the examples in FIG. 5 wanting not only for the disease information but for lifestyle, medications being taken, digital medication diagnostic and tracking devices, and environmental input, etc.
  • FIG. 6 The exemplary embodiment of a Drug Specific Dispensing Algorithm 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 132, 134, 136, 138, 140, 142, 144, 146, 148, 150, 152 is illustrative of the Decision Tree, sequencing, and messaging that is utilized by each Drug Specific Dispensing Algorithm 15. Biometric Authorization 120, 121, Product Expiration 122, and Properly Stored 123 are constant variables in the dispensing decision. The respective messages are either standard, as an example those related to locking the Drug Dispenser 130, 136, 142, 148 or Notify Call Center 132, 138, 144, 150, or Product Expired 132, 134 or the drug was not Properly Stored 138, 140, etc. Screens indicating why a drug is not “Allowed to Dispense” are specifically adapted to the drug and report the reasons why the drug was not dispensed 144, 146. Each Drug Specific Dispensing Algorithm 15 is specifically developed to control the dispensing of a specific medication.
  • FIGS. 7A and 7B present the exemplary embodiment illustration of the Patient 50 interaction to dispense, as example, alosetron, a 5HT3 antagonist for the treatment of diarrhea predominant irritable bowel syndrome (IBS-D). The process begins by the Drug Dispensing App 160 alerting the Patient 50 that it is time to take his/her medication. If it is on a smart phone, it also changes the screen to the Drug Dispenser App 160 graphic′ and when the Patient 50 unlocks the phone, the screen automatically changes to the Biometric Authentication screen 162. Alternatively, the Patient 50 can click on the Drug Dispensing App 160 for alosetron, this is automatically followed by a Biometric Authentication screen 162, upon authentication, the screen automatically moves to the Patient Self- Assessment screens 164, 166, 168, 170. A click on a value of the self-assessment screen automatically moves the process to the next screen. If nothing is found to block dispensing by the alosetron Drug Specific Dispensing Algorithm 15, then the Patient 15 sees the Dispense screen 172. By clicking on Dispense, the patient is then able to go to the related Drug Dispenser 30 and click, for example, on top of the dispenser to dispense a single dose—after which the Drug Dispenser goes back to a locked position. If the Patient 50 wants to change a prior entry before dispensing, he/she can use the devices scroll back capabilities to return to the right screen and change the selection. If the alosetron Drug Specific Dispensing Algorithm 15 finds any reason not to allow dispensing, it selects from the appropriate drug specific screen to show why dispensing was rejected and to facilitate the Patient's ability to avail himself/herself of the proper medication support 176, 178, 180.
  • FIGS. 8A-8D are an exemplary embodiment of the alosetron Drug Specific App configured to capture all the Patient Self-Assessment information which is required by the FDA or EMA for the approval of a 5HT3 drug. The only difference to FIGS. 7A and 7B are the additional input screens 200, 202, 204, 208, 210, 212, 214 required by the regulatory agencies. The same Drug Specific Dispensing Algorithm 15, decision tree, would be used for the clinical trial configuration as for the alosetron example in FIGS. 7A and 7B.
  • The embodiment is applicable for, as an example, clinical trials, post-launch surveillance, for the FDA's Risk Evaluation and Mitigation Strategy (REMS) programs, and to control and ensure drugs are efficacious and safe as dispensed within the Drug Specific Dispensing Algorithm 15 as part of a prescribed drug regimen, etc.
  • FIG. 9 is an exemplary embodiment illustration of the Drug Dispenser 230, 232, 234 designed to be: (i) controlled by a Drug Specific App 10 resident on an Interface Device 20, (ii) water proof, (iii) tamper resistant, (iv) withstand being dropped and/or banged, to be rugged, (v) operate and withstand hot and cold temperatures within defined temperature ranges, (vi) reusable, (vii) rechargeable, and (viii) small enough to be carried in a pants pocket or purse. The Drug Dispenser 230 automatically recognizes the drug based upon the Drug Specific Drug Cassette 240 docked into the device. The Drug Specific Drug Cassette 240 can only be docked or removed by a healthcare professional. The Drug Dispenser 230 remains locked from dispensing unless it receives an encrypted signal from the authorized Drug Specific App 10. The Drug Dispenser 230 dispenses the drug with one click.
  • The Drug Dispenser 230 when interfaced through a digital handshake with the drug specific App transmits for example: (i) its serial number, (ii) the drug information on the Drug Specific Drug Cassette 240, (iii) current and historic temperatures since the last dispense, (iv) humidity exposure since the last dispense, and (iv) the date and time the drug was last dispensed.
  • FIG. 10 is an exemplary embodiment illustration of the Drug Specific Drug Cassette 240 designed: (i) to use approved drug packaging materials, (ii) to dock into the Drug Dispenser 242, 244, and (iii) as a blank cartridge which can accommodate a number of different pills, caplets, capsules, etc. within a specified size range. The blank Drug Specific Drug Cassette 240 is designed to be proprietary to the Drug Dispenser 230 and is marked, as part of the automated cassette fill operation, to allow the Drug Dispenser 230 to ascertain the: (i) name of the drug (brand and/or generic), (ii) drug's NDC number, (iii) drug batch number, (iv) drug's expiration date, etc. The cassette closure is designed to allow printing or any required regulatory information.
  • FIG. 11 presents exemplary embodiment of the Patient 50 specific charts 250, 252, 254 which illustrate the relationship between when the Patient 50 took their medication versus his/her self-assessment or digitally captured symptoms and/or diagnostic values. This clearly shows the relationship between the medication and symptoms. The charts or tables, which can be requested and viewed by the Patient 50 on the Interface Device 20 are designed to educate the patient and promote Patient 50 prescription compliance and persistence.
  • Prescribers 60 can utilize the information to ensure the medication is efficacious for the individual Patient 50, to titrate dosing, and to personalize drug therapy (for personalized medicine).
  • The respective charts, graphs, reports, etc. may be generated by the Drug Specific App 10 and/or by the Integrated Support Centers 40 centralized analytics platform.
  • FIG. 12 is an exemplary embodiment illustration of Drug Dispensers designed to serve the needs of most Patients 50. Approximately half of all Patients 50 take two medications and 20 percent take five or more. Consolidated Therapy App 270 automatically senses other Drug Specific Apps 10 that or on the Interface Device 20. It consolidates from two to many Drug Specific Apps 10 into a single user interface for all drugs—eliminating duplicate logins, entries, and record keeping. It in turn digitally handshakes with the Multi-Drug Dispenser 280 and uses the individual Drug Specific Dispensing Algorithms to control dispensing of each individual medication. Furthermore, it coordinates the dispensing schedules to have as few dispensing times, within the respective prescriptions, as possible. Multi-Drug Dispenser eliminates concerns about which drugs have to be taken when.
  • Illustrations 282, 284, 286, and 288 are exemplary of dispensing units containing from two drugs to five drugs. These units are standalone or can be docked into a Multi-Dispenser desktop unit.
  • FIG. 13 is an exemplary embodiment of the Drug Dispenser 292 and the Drug Specific App 294 interfaces with the: (i) centralized Servers, (ii) databases, and (iii) Analytics systems (the IT System 290), through the Interface Device 294 e, to ensure the Patient 304 is receiving the best care, tailored to the Patient (“personalized medicine”), for the prescribed Drug.
  • All the data collected by the Drug Specific App 294, from the Drug Dispenser 292, Digitally Captured Information 294 a, 294 b, 294 c, the Patient Self- Assessment screens 100, 102, 104 contained within the Drug Specific App 294, and the respective output of the Drug Specific Dispensing Algorithm 15 are transmitted by the Drug Specific App 294 through the Interface Device 294 e to the appropriate Patient database on the centralized Servers 290. The data is utilized to update the respective patient screens used by the Disease Management Counselors in the Integrated Support Center. The data is also made available to the respective Drug Registries 306 and the related Electronic Medical Record 296. Any information that requires a communication with the Patient 304 and/or the Prescriber 308 is handled either automatically by the patient management software or by the Integrated Support Center 302.
  • The patient's information is continually analyzed by the analytical routines both individually for the patient as well as in comparison with treatment data from other like patients to ascertain if any changes in therapy may be warranted. This analytical capability is utilized by the Integrated Support Center 302 to assist Prescribers 308 when they are trying to develop a treatment plan for difficult patients. The Analytics 290 performed may include the patient's data, pooled patient information, as well as information from Electronic Medical Records 296, clinical studies, and publications, etc.
  • As further example of the embodiment, the centralized Servers and Analytics 290 provide the following, as well as other, exemplary backbone support:
  • For the Drug Specific App 294: (i) assigns the App to a specific Patient 304, (ii) links the Drug Dispenser 292 to the Drug Specific App 294 which in turn limits the dispenser and App only to work with one another, (iii) stores the App codes on server, and (iv) enables and updates the Drug Specific App software via communication with the Interface Device 294 e, etc.
  • For the Drug Dispenser 292: (i) stores all reported data in the designated databases on the Servers 290, (ii) syncs the patient data on all the respective Interface Devices 294 e; (iii) stores dispensing, dispensing attempts, lock, and malfunction data; (iv) transmits reports to patient via the Drug Specific App 294 on request; (v) enables lock or unlock transmission from the Integrated Support Center 302; changes the Drug prescription on the Drug Specific App 294 as imputed by the Disease Management Represented per the Prescribers 308 instructions, and (vi) stores the authorized medical professional identification code required for the professional to open the Drug Dispenser 292 in order to change or load the Drug Specific Drug Cassette 242, etc.
  • For the Integrated Support Center 302: (i) aggregate patient data, (ii) presents and updates data on patient specific Managed Care call center screens, (iii) provides the ability to change a Patient's 304 prescription, (iv) enables the remote locking and unlocking of individual Drug Dispensers 292 via their Drug Specific App, (v) enable drug specific transmissions to all Patients 304, (vi) enables simultaneously locking all Drug Dispenser 292 for a specific Drug in the event of a Drug recall, and enables medical professionals to open, load, and close the Drug Dispenser 292, etc.
  • For the Patient 304: (i) prepares patient specific communications, (ii) creates personalized charts and reports, and (iii) generates “Payer Outcomes Reports”, etc.
  • For Registries 306: (i) maintains the Registry 306, Electronic Medical Record 296 and App databases and analytics. (ii) prepares Therapy efficacy reports, (iii) prepares best practices reports, and (iv) through the Integrated Support Center provides Patient 304 specific diagnosis and therapy assistance to Prescribers 308 as requested.
  • For the Prescriber 308: (i) prepares and sends Patient 304 alerts, (ii) conducts meta-data analysis, prepares Patient specific reports and shares the results with the Prescriber 308, (iii) provides the Prescriber 308, through the Integrated Support Center 302, assistance/guidance based upon Prescriber 308 requested database and analytics queries, and (iv) prepares best practices reports based upon patient and Electronic Medical Records 296 meta-data analysis, etc.
  • For Electronic Medical Records 296: (i) interfaces with the Electronic Medical Record 296, (ii) updates Patient 304 dispensing, compliance, and persistence information, (iii) updates any Integrated Support Center counseling notes, and (iv) extracts patient data, within HIPAA guidelines, for meta-data analysis, etc.
  • FIG. 14 is an exemplary embodiment illustration of how the Integrated Support Center 310 interfaces with the Drug Specific App 312, the Patient 314, the Prescriber 318, and the Electronic Medical Record 316.
  • The Integrated Support Center's 310 interactions with the Patient 314 can be instigated by a number of different scenarios and take on many different forms. Examples include but are not limited to: (i) receipt of a patient alert from the Patient's Drug Specific Drug App 312; (ii) Patient 314 calls; (iii) answering Patient 314 questions about the device, App, the drug, or their therapy; (iv) Patient 314 counseling within the support center's guidelines; (v) locking the individual patient's Drug Dispenser 30 based upon: (a) an Drug Specific App alert, (b) an Integrated Support Center Analytics alert, (c) a patient conversation, etc.; (vi) unlocking the individual patient's Drug Dispenser 30 based upon: (a) a conversation with the Patient 314, (b) a conversation with the Prescriber 318, etc.
  • In addition, as an example, the Integrated Support Center 310 provides: (i) “Compliance” and “Adherence” support; (ii) outbound patient telephone calls; (iii) patient monitoring; (iv) emails and/or calls the patient's physician to recommend therapy change, etc.; (v) patient disease management education; (vi) ensures patient has access to their drug; (vii) as required, works with payers to obtain coverage for high cost medications; (viii) looks for prescription financial assistance programs; (ix) patient education and reeducation; (x) patient follow-up, and (xi) Medical Affairs support.
  • The Integrated Support Center's 310 interactions with the Prescriber 318 can be instigated by a number of different scenarios and take on many different forms. Examples include but are not limited to: (i) locking or unlocking a specific patient's Drug Dispenser 30; (ii) changing the prescription; (iii) patient specific physician support using the Integrated Support Center's 310 Analytics 290 to ascertain patient specific treatment alternatives; (iv) assist with patient specific data analysis; (v) provide disease/condition specific information; and (vi) Medical Affairs support, etc.
  • FIG. 15 illustrates an exemplary embodiment of the design of a single drug Drug Dispenser 324. The size of said dispenser 324 in the exemplary being 3.8 inches tall by 2.5 inches wide by 9/16th inches wide. The design incorporates a clam shell design 320, 330 with a pivot on one corner and a tamper resistant and waterproof seal on the opposite edge right before the corner. All design work meets the respective FDA 21 CFR 820 Quality System Regulation, design center ISO 13485:2003 certification and Risk Management process for design, ISO14971, requirements. The Drug Dispenser 320, 322, 324, 326, 328, 330 has been designed for manufacturing (on both PCB and plastics or sheet metal parts), assembly (PCBA and Box Build), and cost. The design incorporates failure modes and effects analysis (FMEA) to address all possible failures in design, manufacturing, assembly, interface with the Drug Specific App 10 or when used by a patient. It is designed for testing, continual design improvement, the environment, and reliability.
  • FIG. 16 is an exemplary embodiment illustration of the assembly and locking mechanism for the Drug Dispenser's 332 clamshell design. The interior of the top of the clamshell 334 incorporates hinges that marry with the hinges on the inside of the bottom clamshell interior 338. These are locked together with a hinge pin 336 that is treaded through the holes in the respective hinges, much the same as the hinges are held together on most common entry doors.
  • The top 334 and bottom 348 clamshells are locked closed and together by use of a microactuator moved locking bar 342. When the top of the clamshell is closed with the bottom clamshell, the locking bar is pulled down by the microactuator and the hook's male member docks into the the female orifice on the locking buttoms 344.
  • The design incorporates integrated supports 354 to ensure the intergrity and durability of the design. They are also instrumental in addind strength, as required, for adding anchors for the respecitive Drug Dispenser 332 components.
  • The design eliminates the ability to open the Drug Dispenser without an authorized signal to cause the microactuator to unlock 342. The Top Cap 340 is fitted to close the top of the Bottom Clamshell. The top of the Top Cap 340 covers the top of the Hinge Pin 336 and holds it in place. The Bottom Cap 350 covers the bottom of the Hinge Pin 336 and holds it in place.
  • The right interior to the Top Cap provides for a dock for the end of the Lock Bar 342 and allows it to move up and down, to lock or unlock, as required. The Bottom Cap 350 provides the seat that supports the Microacturator 342 that lock and unlocks the clamshell by moving the Lock Bar 342 up and down.
  • The Top 340 and Bottom 350 Caps are secured to the Bottom Clamshell Interior 348 by screws that securely marry each of the pieces together. The unit then forms a ridged platform for the Top Clamshell Interior 334 to dock with. When the Drug Dispenser 332 is closed, it forms a sturdy, tamper resistant housing for the Drug Specific Drug Cassette 240.
  • In order to provide the requisite downward pressure to ensure the unit is both water and dust resistant and to contribute to its rugged design, the Drug Dispenser 332 has a Clasp Lock 346 designed to exert the desired level of pressure on the closing joints to secure design integrity.
  • In this embodiment, the Top Cap 338 incorporate the one click dispensing button. The Bottom Cap 352 houses the dispensing port.
  • FIG. 17 is an exemplary embodiment of the Drug Dispenser's 324 electronics and features schematic. The Drug Dispenser's 324 system is comprised of an Applications Processor 368 that contains the units Firmware, individual Drug Dispenser 324 serial number, and manages all functions. The main unit components are the: (i) communications connectivity 362 module, (ii) its data transfer capability 366, (iii) the units sensors and/or applications 364 that allow the unit to authenticate the user, sense efforts to tamper/open the unit without authority, measure drug storage temperature and humidity, to time time stamp an action or event (clock function), and locate the unit via GPS; (iv) the display module 370; (v) the Power Management and recharge system 376; (vi) Memory management 374; (vii) Cassette Controller which rotates the Drug Specific Drug Cassette 240 which enables dispensing as well as the unit to read specific drug cassette information; (viii) the Dosage Dispenser system 372; and (ix) the various components designed to facilitate and protect the different system functions.
  • FIG. 18 is an exemplary embodiment of the placement of electronics and mechanical components on the outside and within the Drug Dispenser. The front of the Drug Dispenser 380 contains an On Off Button 382 which the user can depress if the Drug Dispenser 380 does not automatically come on when the Drug Specific App 10 handshakes with the Drug Dispenser 380. When a handshake is effectuated or the On Off Button 382 are pushed, a blue led light comes on 384. The light 384 turns to green if the unit is ready to dispense, yellow 384 if it is awaiting authority to dispense, and red 384 if the unit is locked and will not dispense. The display on 386 resides on the center of the face, Front View, of the Drug Dispenser 380.
  • A number of components fit on the Top Clamshell Interior 388; these include: (i) the On Off Button 382 switch 390, (ii) the LED status light 384 LED and electronics 394; (iii) the battery, power management, Wi-Fi, Bluetooth, GPS and antenna systems 392; (iv) the LED Screen 386 electronics and management system 396; and (v) the drug dispensing actuator arm and dispensing lock 398. The Bottom Clamshell Interior 400 houses the: (vi) single click Dispensing Button 402; (vii) the Logic, Controls, Processor and Memory Board and its various components 404; (viii) Temperature and Humidity sensors 406; (iv) the Attempting Tampering Sensors 412; (x) the Cassette Rotation Motor and Controller (works like a CD-Rom rotator) 410; (xi) the Drug Cassette Reader 408; (xii) the Clamshell Lock microactuator controller 414, and (xiii) the Dispensing Door Controller 416.
  • IV. Examples
  • The embodiment of the invention can be utilized, for among other uses, 1) to improve the drug's safety profile by ensuring proper, personalized drug utilization (e.g., Dispensing), 2) as a diagnostic aid/tool, 3) to preclude drug related adverse events, 4) to decrease the chance of addiction, 5) to preclude overdosing, 6) to manage drug dependence withdrawal, 7) to manage oral patient controlled analgesia, 7) to preclude drug divergence, 8) to guard the medication against accidental ingestion by a child, and 9) to capture the information required and control drug dispensing during clinical trials.
  • A. Dispensing
  • Ensuring the proper utilization of antihypertensive medications serves as an example of how the embodiment can be used to ensure proper drug utilization. As patients get older, they have a tendency to gain weight and to develop comorbidities. These factors can interfere with how the medication is metabolized and alter the need or effectiveness of the drug over time. As a result, certain patients may become dizzy or faint as a result of a hypotensive event. If the patient is prescribed an antihypertensive, it is beneficial to prevent a potential hypotensive event, especially as it may lead to an untoward accident.
  • Under the current embodiment, the patient would be prescribed an antihypertensive dispensed using the Drug Specific App 10 controlled Drug Dispenser 30. When the Patient 50 clicks on the Drug Specific App 10 to take his/her next dose, the Drug Specific Dispensing Algorithm 15 would automatically check to ensure the drug has not expired, and if it has not, then to see if it has been stored correctly, and if the Drug has been stored correctly, then, for example, it would handshake with designated devices to digitally capture blood pressure and heart rate information. Thereafter, it asks the Patient 50 at least one Patient Self-Assessment question. Examples include but are not limited to: (i) have you gotten dizzy since the last time you took your antihypertensive medication, (ii) do you have blurry vision, (iii) have you felt like fainting since you took your last antihypertensive, etc. If the patient answered yes to any of the Patient Self-Assessment questions, the Drug Specific Dispensing Algorithm 15 would check the trending of the Patient's 50 blood pressure and heart rate information since the last dose. If the indication would be that the Patient 50 may suffer a hypotensive event as defined by the Decision Tree, the Drug Specific Dispensing Algorithm 15 would lock the Drug Dispenser 30 and inform the Patient 50 that he/she should call the Integrated Support Center 40 or talk with their Prescriber 60 or a physician prior to being able to dispense the next dose, even if the dose is within prescribing parameters. After talking with the Patient 50, the Disease Management representative at the Integrated Support Center 40 can decide within their operating constraints whether or not to unlock the Drug Dispenser 30 and allow the Patient 50 to dispense and take the prescribe antihypertensive. If not appropriate, the representative would send an email, text, and/or call the Prescriber 60 to advise him/her that an adjustment has to be made to the Patient's 50 hypertension treatment. The Drug Dispenser 30 can then be unlocked and allowed to dispense the medication if those are the Prescriber's 60 instructions or the prescription can be changed based upon the Prescriber's 60 instructions.
  • In the process, an accident and/or costlier intervention can be averted, the drug efficacy for the specific Patient 50 is assured, the patient's quality of care is personalized and improved, and the patient's quality of life is enhanced.
  • B. Diagnostic
  • The embodiment of the Invention can also be utilized to assist in diagnosis. As an example, there are many different types of pain and different types of headaches. Patients will generally begin by self-medicating with over the counter (OTC) analgesics such as aspirin. As the pain or discomfort increases, patients increase the number of tablets taken (i.e., the dosage), as well as the frequency of self-medication. At a certain point, they go to their doctor seeking adequate relief.
  • When the doctor talks with the Patient 50, he/she may describe many different types of pain, making it difficult to diagnose. Pain has multiple causes, and people respond to it in multiple and individual ways. The pain that one person pushes their way through might be incapacitating to someone else.
  • Headaches represents an example. It is important to figure out what type of headache is causing the pain. If the doctor knows the type of headache, he/she can treat it correctly. However, as was highlighted by a 2004 study, 80% of people who had a recent history of self-described or doctor-diagnosed sinus headache, but no signs of sinus infection, actually met the criteria for migraine. The following discusses the different types of headaches:
      • 1) Tension headaches, the most common type of headache, can generally be adequately treated with over-the-counter treatments such as aspirin, ibuprofen, or acetaminophen (Tylenol). Experts believe these may be caused by the contraction of neck and scalp muscles (including in response to stress), and possibly changes in brain chemicals.
      • 2) Cluster headaches, which affect more men than women, are recurring headaches that occur in groups or cycles. They appear suddenly and are characterized by severe, debilitating pain on one side of the head, and are often accompanied by a watery eye and nasal congestion or a runny nose on the same side of the face. During an attack, people often feel restless and unable to get comfortable; they are unlikely to lie down, as someone with a migraine might. The cause of cluster headaches is unknown, but there may be a genetic component. There is no cure, but medication can cut the frequency and duration.
      • 3) Sinus headaches occur when a sinus becomes inflamed, often due to an infection. They can generally be diagnosed by symptoms or the presence of pus viewed through a fiber-optic scope. Headaches due to sinus infection can be treated with antibiotics, as well as antihistamines or decongestants.
      • 4) Rebound headaches, ironically, can be caused by the overuse of painkillers for headaches. Culprits include over-the-counter medications like aspirin, acetaminophen (Tylenol), or ibuprofen (Motrin, Advil), as well as prescription drugs.
      • 5) Migraine headaches can run in families and are diagnosed using certain criteria: (i) at least five previous episodes of headaches, (ii) last between 4-72 hours, (iii) at least two out of four headaches have one-sided pain, throbbing pain, moderate-to-severe pain, and pain that interferes with, is worsened by, or prohibits routine activity, and (iv) at least one of the following is associated with the pain: nausea and/or vomiting, or, if those are not present, then sensitivity to light and sound. A migraine may be foreshadowed by aura, such as visual distortions or hand numbness. (About 15 percent to 20 percent of people with migraines experience these.)
      • 6) Mixed headache syndrome, also called transformed migraines, is a combination of migraine and tension headaches.
      • 7) Acute headaches are headaches that occur suddenly and have symptoms that subside after a relatively short period of time.
      • 8) Hormone headaches are often associated with women's changing hormone levels during menstruation, pregnancy, and menopause. Chemically induced hormone changes, such as with birth control pills, also trigger headaches in some women.
      • 9) Chronic progressive headaches also called traction or inflammatory headaches, are chronic progressive headaches that get worse and happen more often over time. These are the least common type of headache, accounting for less than five percent of all headaches in adults and less than two percent of all headaches in kids. Chronic progressive headaches may be the result of an illness or disorder of the brain or skull.
  • Diagnosis requires a headache evaluation that includes: (i) headache history, (ii) description of the headaches, (iii) headache symptoms, (iv) characteristics, (v) a list of things that cause the headache, (vi) aggravate the headache, and (vii) things the patient has done to relieve a headache. The patient is also requested to keep a headache diary.
  • The proper treatment will depend on several factors, including the type and frequency of the headache and its cause. There are many migraine and headache medications and other treatments are available. The appropriate treatment often depends on the type of headache.
  • Headache pain may need to be managed with medications. Headache drugs used to treat headache pain can be grouped into three different categories: symptomatic relief (drugs used to treat the headache pain or accompanying symptoms of migraines like nausea), abortive therapy (drugs used to stop a migraine headache), and preventive therapy (drugs used to prevent a migraine). Botox injections represents another migraine and headache treatment.
  • The way the body responds to migraine and headache medications may change over time, so medications may need to be adjusted.
  • The embodiment of the Invention enables the aggregation of Patient 50 specific dispensing information and Patient Self-Assessment information specifically developed to assist in the diagnosis and management of headaches.
  • C. Management of Complex Drug Therapy
  • Cystic fibrosis (CF) serves as an example of how the system can be utilized to manage complex drug therapy. There is no cure for CF, but treatment can ease symptoms and reduce complications, physician office visits and hospitalizations. Close monitoring and early, aggressive intervention is recommended.
  • Managing CF is complex, so treatment is best if managed by a center that specializes in cystic fibrosis. The goals of treatment include: (i) preventing and controlling lung infections, (ii) loosening and removing mucus from the lungs, (iii) preventing and treating intestinal blockage, (iv) providing adequate nutrition, and (v) medications.
  • The patient must take multiple drugs, the schedule and combination which must be personalized for each patient. The medicines include those to help treat or prevent lung infections, reduce swelling and open up the airways, and thin mucus. If the patient has mutations in a gene called G551D, which occurs in about 5 percent of people who have CF, the doctor may prescribe the oral medicine ivacaftor (approved for people with CF who are 6 years of age and older). Adherence and persistence with each drug regimen is critical to avoid costly complications. The options include:
      • a. antibiotics to treat and prevent lung infections (Most people with CF have ongoing, low-grade lung infections. Sometimes, these infections become so serious that the patient may need to be hospitalized. Antibiotics are the primary treatment.)
      • b. mucus-thinning drugs to help the patient cough up the mucus, which improves lung function.
      • c. bronchodilators to help keep the airways open by relaxing the muscles around the bronchial tubes, and
      • d. oral pancreatic enzymes to help your digestive tract absorb nutrients.
  • The embodiment of the Invention enables the complex management of the CF Patient 50 via the utilization of the Multi-Drug Dispenser 280. The Consolidated Therapy App 270 consolidates from two to as many Drug Specific Apps 10 as are resident on the Interface Device 20 into a single user interface for all drugs—eliminating duplicate logins, entries, and record keeping. It in turn digitally handshakes with the Multi-Drug Dispenser 280 and uses the individual Drug Specific Dispensing Algorithms 15 to control dispensing of each individual medication. Furthermore, it coordinates the dispensing schedules to have as few dispensing times, within the respective prescriptions, as possible. Multi-Drug Dispenser 280 eliminates concerns about which drugs have to be taken when. It can also be programmed to provide alerts for the patient to take his/her related injectable and/or inhaled medications. In this way, the Dispensing System simplifies CF drug management, encourages prescription compliance and persistence, avoids complications, and thereby reduces the total cost of treating a CF patient by decreasing the number of physician interventions and hospitalizations.
  • D. Opioids
  • Opioid medications (examples include: codeine, fentanyl and analogs, hydrocodone, hydromorphone, methadone, oxycodone, Oxymorphone, etc.) are effective in controlling pain. However, physicians are reluctant to prescribe them due to their overdose, abuse, addiction and divergence potential and related REMS programs. Some patients are also reluctant to take them due to their addiction potential. The embodiment provides control and real time monitoring and thereby address each of these shortcomings.
  • Overdosing is addressed by the inability of the patient to dispense a dose more frequently than allowed by the prescription. This is handled by the Drug Specific Dispensing Algorithm 15 which controls dispensing by the Drug Dispenser 30.
  • Abuse is addressed by the design of the tamper resistant Drug Dispenser 230. The Drug Specific Drug Cassette 240 can only be docked with the Drug Dispenser 244 by an authorized medical professional. Any attempt by an unauthorized person to open the Drug Dispenser 244 triggers a signal to the Drug Specific App 10 which automatically locks the Drug Dispenser 244 and alerts the Integrated Support Center 40. The Integrated Support Center 40 then calls the Patient 50 to ascertain why they are trying to open the Drug Dispenser 30. At this point, the Integrated Support Center 40 works with the Patient 50 to address any dispensing related issues and unlocks the Drug Dispenser 30 or, if attempted abuse is suspected, contacts the Prescriber 60 to alert them of the conversation with the Patient 50 and asks the Prescriber 60 whether or not the Drug Dispenser 30 should remain locked or if it should be unlocked. If authorized, the Integrated Support Center 40 updates the Electronic Medical Record 70 related to the calls to the Patient 50 and the Prescriber 60.
  • The potential for addiction is mitigated by: (i) the patient's inability to dose more frequently than the prescribed medication schedule, (ii) by tracking attempted earlier than prescribed dosing events, (iii) by capturing any attempts to open the Drug Dispenser 30, and (iv) through the use of patient self- assessment 100, 102, 104 and/or digitally captured relevant information, trended over time, to ascertain the effectiveness of the drug on the specific patient. The centralized drug specific patient and population focused analytics programs 290 are designed to take a myriad of patient specific actions and inputs into account in order to identify potential movement of the Patient 50 toward addiction. When potential addiction is identified, the analytics software 290 is programmed to alert the Integrated Support Center 40 so they may alert the Prescriber 60 and update the patient's Electronic Medical Record 70.
  • Divergence is precluded by a number of combined features: (i) the serial number of the Drug Specific Drug Cassette 240 and the drug's batch number are digitally married to the Drug Dispenser 244, (ii) the serial number of the Drug Dispenser 230 is linked to the Patient's Drug Specific App 10, (iii) the use of the Drug Specific App is restricted to a specific Patient 50, and (iv) the Drug Specific App 10 requires a biometric login 90 to access the Drug Specific App 10 in order to instruct the Drug Dispenser 230 to dispense the drug. The unit further supplies additional control of the drug being taken can be tracked with RFID tracking which would allow the Drug Specific App 10 to track the drug until it is ingested by the patient. The time interval between the time the drug is dispensed and the time it is ingested, over time, provides an indication of compliance or abuse. When coupled with mega-data analytics conducted by the Integrated Support Center, the probability of accurately identifying potential abusers is significantly increased.
  • The system is designed to comply with the respective REMS program and to virtually eliminate required data capture and automate patient specific tracking and dispensing report preparation. The Integrated Support Center 40 will also support the Prescriber 60 by preparing the required REMS reports encompassing all his/her patients.
  • The system also allows for the redefinition of Prescription Drug Monitoring Programs by closing the loop between pharmacies and healthcare providers and the patient by controlling and tracking use on an individual patient basis.
  • Attributes of the system enable oral patient controlled analgesia. Studies have shown that patients that have the ability to self-medicate as warranted, e.g., PRN with set prescription parameters, tend to use less medication, further mitigating potential side effects.
  • The system may also be utilized to predict, for example, opioid related constipation and to alert the patient to take a laxative at the appropriate time. If the system's multi-drug dispenser is utilized, the program can dispense the laxative as well as the opioid and/or other medication as prescribed.
  • E. Addiction and Withdrawal
  • Addiction is a global crisis with an estimated 2.4 million opioid-dependent people in United States, 1.3 million in Europe and twenty million in the rest of the world. Opioid overdose is the second leading cause of accidental death in the US. Overdoses claimed 16,000 lives in the United States alone in 2012.
  • If other kinds of addiction are added, 4.5% of disease and injury around the globe can be attributed to alcohol, and these numbers are most likely underreported. The true population that suffers from opioid, prescription drug, and alcohol addiction is estimated to be much greater.
  • Addiction can either be treated with buprenorphine and/or naloxone (examples of brand names include Butrans, Suboxone, Zubsolv). In cases of physical dependent, withdrawal must be managed through the gradual decrease of doses of the dependent drug (e.g., barbiturates, benzodiazepines, methamphetamines, narcotics, opioids, methadone, etc.).
  • Appropriate precautions must be taken to minimize risk of misuse, abuse, or diversion, appropriate protection from theft, and unintended pediatric exposure; much the same as with the opioids. In addition, appropriate clinical monitoring as to the patient's level of stability is essential. The embodiment of the system provides control and real time monitoring and thereby address each of these shortcomings.
  • Overdosing is addressed by the inability of the patient to dispense a dose more frequently than allowed by the prescription. This is handled by the Drug Specific Dispensing Algorithm 15 which controls dispensing by the Drug Dispenser 30. The controls are in place even for the Drug Specific App 10 and Drug Dispenser 30 enabled oral PRN dosing regimen.
  • Abuse is addressed by the design of the tamper resistant Drug Dispenser 230. The Drug Specific Drug Cassette 240 can only be docked with the Drug Dispenser 244 by an authorized medical professional. Any attempt by an unauthorized person to open the Drug Dispenser 244 triggers a signal to the Drug Specific App 10 which automatically locks the Drug Dispenser 244 and alerts the Integrated Support Center 40. The Integrated Support Center 40 then calls the Patient 50 to ascertain why they are trying to open the Drug Dispenser 30. At this point, the Integrated Support Center 40 works with the Patient 50 to address any dispensing related issues and unlocks the Drug Dispenser 30 or, if attempted abuse is suspected, contacts the Prescriber 60 to alert them of the conversation with the Patient 50 and asks the Prescriber 60 whether or not the Drug Dispenser 30 should remain locked or if it should be unlocked. If authorized, the Integrated Support Center 40 updates the Electronic Medical Record 70 related to the calls to the Patient 50 and the Prescriber 60.
  • The potential for addiction is mitigated by: (i) the patient's inability to dose more frequently than the prescribed medication schedule, (ii) by tracking attempted earlier than prescribed dosing events, (iii) by capturing any attempts to open the Drug Dispenser 30, and (iv) through the use of patient self- assessment 100, 102, 104 and/or digitally captured relevant information, trended over time, to ascertain the effectiveness of the drug on the specific patient. The centralized drug specific patient and population focused analytics programs 290 are designed to take a myriad of patient specific actions and inputs into account in order to identify potential movement of the Patient 50 toward addiction. When potential addiction is identified, the analytics software 290 is programmed to alert the Integrated Support Center 40 so they may alert the Prescriber 60 and update the patient's Electronic Medical Record 70.
  • Divergence is precluded by a number of combined features: (i) the serial number of the Drug Specific Drug Cassette 240 and the drug's batch number are digitally married to the Drug Dispenser 244, (ii) the serial number of the Drug Dispenser 230 is linked to the Patient's Drug Specific App 10, (iii) the use of the Drug Specific App is restricted to a specific Patient 50, and (iv) the Drug Specific App 10 requires a biometric login 90 to access the Drug Specific App 10 in order to instruct the Drug Dispenser 230 to dispense the drug.
  • The system is designed to comply with the respective REMS program and to virtually eliminate required data capture and automate patient specific tracking and dispensing report preparation. The Integrated Support Center 40 will also support the Prescriber 60 by preparing the required REMS reports encompassing all his/her patients.
  • F. Clinical Trial
  • The system is designed to capture, store, analyze, and act upon drug specific patient reported self-assessment (AKA self-reported outcomes, patient-reported outcomes, PROs, etc.) and digitally captured physiological, psychological, lifestyle, other drugs currently being taken, and environmental information along with the drug's prescription and drug dispensing history in order for the Drug Specific App 10 to decide if the drug should or should not be dispensed. Dispensing can be precluded by the Drug Specific App 15 if the required dispensing criteria are not met, even if without the self assessment and digitally captured data, the prescription would normally allow dispensing.
  • Most of the time, clinical outcomes are held as the ultimate outcome in a clinical trial because they often provide more objective interpretation, increased reliability and greater simplicity of interpretation. However, certain disease conditions require consideration of subjective outcomes. As a result, regulatory agencies, such as the FDA, are combining patient reported outcomes (PROs) and clinical outcomes in their approval decisions. Examples include the: (i) FDA's “Guidance for Industry, Irritable Bowel Syndrome—Clinical Evaluation of Drugs for Treatment”, dated May 2012 and (ii) the European Medicines Agency (EMA) “Guideline on the evaluation of medicinal products for the treatment of irritable bowel syndrome” dated April 2015. They utilize a combination of PROs and patient self-assessment reporting to measure primary and secondary endpoints required for regulatory approval of any 5HT3 drugs for irritable bowel syndrome (IBS).
  • Interest in developing and applying patient-reported outcomes (PROs) across the drug development and postmarket spectrum is growing—among sponsors, clinicians, payers, regulators and patients. A growing number of clinical trials now are going beyond conventional randomized control measurements to collect self-reported outcomes from patients—focusing on improving patients' involvement by including their perspectives throughout the drug development process. An analysis of sponsor-funded interventional studies listed on CenterWatch's Clinical Trials Listing Service found between 2005 and 2007, only 6.1% of total study procedures involved some type of subjective outcome assessment. That grew to 11.8% in the 2008 to 2010 timeframe and, most recently, between 2011 and 2013, increased to 16.3% of total study procedures. PROs can capture a range of information, from symptom changes and level of functioning, to health-related qualify of life and treatment satisfaction and adherence.
  • Although their value is widely recognized, PRO use often is inconsistent and underutilized in understanding how patients feel in relation to their diseases, such as cancer, cardiovascular disease, diabetes, etc. Generally, regulatory agencies do not require sponsors to consider PROs in clinical trials and, until recently, did not do much to encourage their use. However, signs point to that sentiment is changing. Janet Woodcock, M.D., director of the FDA's Center for Drug Evaluation & Research (CDER) stated: “We understand that people with chronic diseases are experts in that disease, as far as the symptoms and the impact on quality of life, and what might be acceptable tradeoffs on risk and uncertainty. The challenge for the FDA is incorporating that knowledge in a way that accurately informs regulatory decisions.” She asked, “how can we meaningfully collect that knowledge in a rigorous manner, given there's a spectrum of opinions and a spectrum of disease burden in any given disease?” PRO measurements often are used to evaluate products that treat chronic, disabling conditions, for which the goal of treatment is focused on alleviating the frequency, severity or duration of disease symptoms.
  • PROs generally are used as primary endpoints in clinical trials in indications such as migraines and irritable bowel syndrome, in which specific symptoms play a major role in treatment. PROs also are important in the final product labeling manufacturers are allowed to use to promote their products, and to clinicians seeking information to support their prescribing choices. Now, trials for psychiatric and age-related illnesses, among others, are including PROs as part of the protocol design.
  • Pain studies initially used PROs as a primary outcome in a clinical trial because attempts to obtain an objective measure of pain through a dolorimeter, a spring-loaded instrument with a gauge for measuring sensitivity to, or levels of, pain, or through a galvanic skin response lacked validity compared to simple pain scales. Other disease examples where PROs are preferable include neurology, depression, anxiety, and irritable bowel syndrome (IBS) which may utilize co-primary and/or key secondary PROs.
  • Keeping trial participants involved also is the hallmark of the publication and promotion of the FDA's PRO guidance at the end of 2009. In 2011, the FDA took the next step, seeking multiple ways to give the patient a clear voice in clinical research by ensuring all measurements and outcomes reflect what is happening with the patient through instruments or tools, along with PROs. Increasingly, we are seeing patients in clinical trials demanding to know what is going on and they want to be given a greater voice.
  • Generally, larger clinical sites can handle adding PROs more easily, while smaller sites, especially in more remote locations, can find it more challenging. Collecting data directly from the patient can provide stronger information. As an example, patients can be hesitant to report outcomes if they have been asked to take a medication a certain way and have not done so.
  • Furthermore, collecting data through specific data streams provides, in some cases, better quality. Patients will contact the independent group, such as the clinical trial CRO or in the embodiment, the Integrated Support Center 40 and not necessarily go back to their physicians for technical issues and concerns.
  • While using PROs is becoming critical in many clinical trials to prove safety and effectiveness to gain FDA approval, the next step for biopharmaceutical companies and payers will be to combine PROs with other observational studies to create real world evidence (RWE). RWE is becoming essential for sound medical coverage, payment and reimbursement decisions, according to the International Society for Pharmaeconomics Outcomes Research Real-World Data Task Force. RWE can be used with randomized clinical trials to design more efficient trials and understand a drug's benefit-risk profile, as well as to gain understanding of the market for launch planning, according to the task force. RWE shows how a drug is accepted from patients who have experience using it. It reveals how a drug is utilized in different geographies and can be used to help frame policy or regulatory decisions. It is a highly credible source of information.
  • The embodiment provides:” (i) the requisite data capture, (ii) patient involvement, (iii) dispensing control, (iv) avoidance of certain drug related side effects, (v) real time reminders for the patient to take the medication, (vi) intervention alerts if the patient fails to take their medication within a predefined time interval, (vii) dispensing tracking (date and time), (viii) real time monitoring, and (ix) reporting. It addresses the shortcomings of current systems to capture and compile real time, patient and drug specific data to facilitate ongoing clinical trial data aggregation, analysis, and reporting while minimizing the number of calls to the clinical trial physician.
  • Under the current embodiment, the patient would be prescribed the medication to be dispensed per a defined prescription using the Drug Specific App 10 controlled Drug Dispenser 30. When the Patient 50 clicks on the Drug Specific App 10 to take his/her next dose, the Drug Specific Dispensing Algorithm 15 automatically handshakes with the Drug Dispenser 30, handshakes with defined digital devices (e.g., blood pressure, heart rate, etc.) FIG. 5 and downloads the latest data to the Interface Device's 20 Drug Specific App 10 data base, checks to ensure the drug has not expired, and if it has not, then to see if it has been stored correctly. If the Drug has been stored correctly, then, for example, it automatically moves to the next screen and asks the Patient 50 to answer the specific questions. In this example, the Patient 50 would answer the PRO and data capture screens 194 to 214 required by the FDA and EMA to get approval for a 5HT3 drug to treat IBS-D. The ability to capture the requisite PRO primary and secondary end point data and the related compliance and persistence data are illustrated in FIG. 8. These screens can be configured to capture and aggregate drug specific information.
  • The Drug Specific Dispensing Algorithm 15 then utilizes its decision tree FIG. 6 to check the prescription instructions and when the drug was last dispensed to ascertain if the drug can be dispensed. It then either generates a screen stating that the dose will not be authorized for a specific period of time 222 or proceeds to ascertain if the designated digital and self-assessment reported values allow the medication to be dispensed. If yes, then the screen shows a green dispense 216. If the Drug Specific Dispensing Algorithm 15 indicates that the patient should not receive the medication, even if it is within the prescription guidelines, then it will either generate, for example, a screen stating that the dose is not warranted at the specific time and provide the Patient 50 the ability to click on dial to call the Integrated Support Center 40 or if a problem is ascertained, it will either show a specifically designed screen or a screen that the Integrated Support Center should be called 224. The type and sequence of screens is dictated by the drug's clinical trial data capture requirements. The algorithm can contain routines that only ask for specific information if certain predefined criteria are met.
  • Every non-fruitful event to dispense the medication is tracked. At a certain point the Drug Specific Dispensing Algorithm's 15 logic will send a message for the Integrated Support Center 40 to call the Patient 50.
  • The embodiment allows for better prescription compliance, an improved drug safety profile, increased prescription persistence, uniform data capture, facilitates data analysis, decreases required interventions by the clinical trial physician(s), decreases the cost of the trial, and provides real time data capture and analysis.
  • G. Intermittent Chronic Conditions
  • There are a number of chronic conditions that come and go and do not always require treatment. Examples include IBS, pain, allergies, arthritis, certain heart conditions, anxiety, depression, intermittent claudication, etc. The Drug Specific App 10 is capable of being programmed to control PRN dosing in various configurations and schedules. This allows for real time data capture which is useful in in diagnosis, patient management, and dispensing control.
  • H. Revitalization of Select Drugs that Previously Failed to Get Regulatory Approval
  • There are a myriad of drugs that failed to get regulatory approval due to dosing-related side effects. Examples include certain 5HT3 antagonists used to treat diarrhea predominant irritable bowel syndrome (IBS-D). Some physicians hypothesize that there is a relationship between dosing (both strength and frequency) and constipation. In turn, that constipation has a relationship with Ischemic colitis.
  • Patients prefer to use PRN dosing. They can take the medication when symptoms arise and continue taking it until they resolve themselves. Lostronex® (alosetron), a 5HT3, approved only in the United States which requires a complex REMS program, serves an example of how the Embodiment can transform drugs that failed to get approval with similar profiles into approvable agents. To lower the risk of constipation, Lostronex® should be started at a dosage of 0.5 mg twice a day. Patients who become constipated at this dosage should stop taking Lostronex® until the constipation resolves. They may be restarted at 0.5 mg once a day. If constipation recurs at the lower dose, Lostronex® should be discontinued immediately.
  • Patients well controlled on 0.5 mg once or twice a day may be maintained on this regimen. If after 4 weeks the dosage is well tolerated but does not adequately control IBS symptoms, then the dosage can be increased to up to 1 mg twice a day. Lostronex® should be discontinued in patients who have not had adequate control of IBS symptoms after 4 weeks of treatment with 1 mg twice a day.
  • Cilansetron, a more potent 5HT3 antagonist for the treatment of IBS-D failed to get FDA and European regulatory approval because of the concerns related to potential constipation that could potentially lead to ischemic colitis. The utilization of the system designed to identify and block dispensing FIG. 4 if potential constipation is suspected would address this concern. If we use the Lotronex® example, the system could also change the dosing to allow PRN dosing using, for example, 0.5 mg for up to four times per day. This would control the maximum dosing to 2 mg per day. The system would ensure compliance with the prescription and would protect against potential constipation.

Claims (61)

1-93. (canceled)
94. A drug dispensing system, comprising:
(i) hardware comprising:
(a) an interface device having a computer processor and memory storing computer code to execute a drug specific app with a plurality of modules wherein the interface device has internet communication capability and is selected from the group consisting of a smart phone, a computer, or a tablet computer wherein the smart phone, the computer or the tablet computer are in communication with a separate drug dispenser device, or wherein the interface device is a standalone tamper-resistant drug dispenser device having a computer processor and memory storing computer code to execute the drug specific app with a plurality of modules, and
(b) at least one digital data capture device and/or at least one RFID drug chip;
wherein the drug specific app is assigned to a specific patient;
(ii) a biometric authentication module to authenticate the patient and to ensure digitally captured data is from the patient;
(iii) a prescription module comprising a prescription for the patient;
(iv) an application program interface (API) (a) between the separate drug dispenser device and the smart phone, the computer or the tablet computer to link the drug dispenser device to the drug specific app, or (b) in the standalone drug dispenser device to link it to the drug specific app;
(v) one or more APIs between (a) the interface device and one or more digital data capture devices, and/or (b) the interface device and one or more RFID drug chips;
(vi) a drug specific dispensing algorithm module; and
(vii) an interface device database module, comprising digitally-captured or patient-entered patient values, drug information, and dispensing-related information;
wherein the system utilizes information selected from the group consisting of prescription information, drug information, drug dispenser device information, patient self-assessment information, digitally captured physiological, psychological, lifestyle information, information of medications administered to the patient, environmental data information, and combinations thereof,
wherein the system captures such information before, during or after each drug dispensing and which is utilized by the drug specific diagnostic algorithm to decide if the separate or standalone drug dispenser device should dispense the drug or preclude dispensing and stay locked even in circumstances when the prescribed dose would have otherwise been allowed by the prescription, thereby preventing dose-mediated adverse events; and
wherein the drug specific diagnostic algorithm further utilizes symptom data obtained from the patient regarding the patient's symptoms and, based on the symptom data, decides if the separate or standalone drug dispenser device should dispense the drug or preclude dispensing and stay locked even in circumstances when the prescribed dose would have otherwise been allowed by the prescription, thereby preventing dose-mediated adverse events.
95. The drug dispensing system according to claim 94, wherein the symptoms analyzed by the drug specific diagnostic algorithm are selected from the group consisting of pupil size, level of pain, stool and bowel movement information, respiratory rate, blood oxygen saturation, pulse, heart rhythm, blood pressure, gait, muscle spasms, and skin temperature.
96. The drug dispensing system according to claim 94, wherein the drug dispenser comprises an opioid.
97. The drug dispensing system according to claim 94, wherein the drug specific dispensing algorithm automatically handshakes with the separate or standalone drug dispenser device and the one or more digital capture devices.
98. The drug dispensing system according to claim 94, wherein the drug specific dispensing algorithm downloads data captured by the one or more digital capture devices to the interface device.
99. The drug dispensing system according to claim 94, wherein the app checks a serial number of the separate or standalone drug dispenser device to ensure it is authorized to interface with the app.
100. The drug dispensing system according to claim 94, wherein the app checks the expiration date of the drug.
101. The drug dispensing system according to claim 94, wherein the app checks the storage temperature history to ensure the drug has been stored within a specific temperature range.
102. The drug dispensing system according to claim 94, wherein the app checks the storage humidity history to ensure the drug has been stored within an authorized humidity range.
103. The drug dispensing system according to claim 94, wherein the app retrieves drug information from the separate or standalone drug dispenser device.
104. The drug dispensing system according to claim 94, wherein the app is designed to receive alerts of unauthorized attempts to open the separate or standalone drug dispenser device.
105. The drug dispensing system according to claim 94, wherein the app stores a drug's prescription and dosing schedule.
106. The drug dispensing system according to claim 94, wherein the app reminds the patient to take his/her medication and after a specific period of time alerts the integrated support center and/or authorized care givers that the patient has not taken his/her medication.
107. The drug dispensing system according to claim 94, wherein the app is designed to automatically handshake with the patient's digital diagnostic, monitoring and/or tracking devices.
108. The drug dispensing system according to claim 94, wherein the app presents drug specific patient self-assessment and/or data input screen(s).
109. The drug dispensing system according to claim 94, wherein the app maintains a database of patient responses captured by self-assessment and/or data input screen(s) and digitally captured values.
110. The drug dispensing system according to claim 94, wherein the interface device is a smart phone.
111. The drug dispensing system according to claim 94, wherein the app allows the patient to click on a screen to automatically call the integrated support center.
112. The drug dispensing system according to claim 94, wherein the app records all unsuccessful attempts to dispense a dose earlier than prescribed.
113. The drug dispensing system according to claim 94, wherein the app has reporting routines that allow the patient to request certain reports created using the patient self-assessment, digital captured information, drug dispenser information, and/or dosing information to ascertain if the drug is efficacious for the patient and the effect that dosing has on the patient's condition and/or symptoms.
114. The drug dispensing system according to claim 94, wherein the app effectuates a handshake with the integrated support center's computers.
115. The drug dispensing system according to claim 94, wherein the app downloads the patient's drug related dispensing information, comprising drug dispenser, patient self-assessment, or digitally captured information into the patient's records in the integrated support center's database.
116. The drug dispensing system according to claim 94, wherein the app allows the patient to request specific drug related information stored in the app.
117. The drug dispensing system according to claim 94, wherein the app allows the patient to request specific reports or information stored on the integrated support center's servers.
118. The drug dispensing system according to claim 94, wherein the app allows the patient to correct responses entered in prior screens before dispensing the medication.
119. The drug dispensing system according to claim 94, wherein the app contains a copy of or enables access to a patient app and drug dispenser operations training and troubleshooting manual.
120. The drug dispensing system according to claim 94, wherein the app further comprises a GPS module to record the patient's location to ascertain where the patient is when the medication is dispensed.
121. The drug dispensing system according to claim 94, wherein the drug dispenser device comprises an integrated drug cassette or a replaceable drug cassette.
122. The drug dispensing system according to claim 98, wherein the drug specific dispensing algorithm prompts the patient self-assessment module to ask the patient one or more questions about his/her condition.
123. The drug dispensing system according to claim 94, wherein the drug dispenser device further comprises a replaceable drug cassette and wherein the app further comprises a security system to limit the ability to change the replaceable drug cassette to an authorized medical professional.
124. A method of treating a patient having a condition or disease utilizing a drug dispensing system, comprising:
(i) hardware comprising:
(a) an interface device having a computer processor and memory storing computer code to execute a drug specific app with a plurality of modules wherein the interface device has internet communication capability and is selected from the group consisting of a smart phone, a computer, or a tablet computer wherein the smart phone, the computer or the tablet computer are in communication with a separate drug dispenser device, or wherein the interface device is a standalone tamper-resistant drug dispenser device having a computer processor and memory storing computer code to execute the drug specific app with a plurality of modules, and
(b) at least one digital data capture device and/or at least one RFID drug chip;
wherein the drug specific app is assigned to a specific patient;
(ii) a biometric authentication module to authenticate the patient and to ensure digitally captured data is from the patient;
(iii) a prescription module comprising a prescription for the patient;
(iv) an application program interface (API) (a) between the separate drug dispenser device and the smart phone, the computer or the tablet computer to link the drug dispenser device to the drug specific app, or (b) in the standalone drug dispenser device to link it to the drug specific app;
(v) one or more APIs between (a) the interface device and one or more digital data capture devices, and/or (b) the interface device and one or more RFID drug chips;
(vi) a drug specific dispensing algorithm module; and
(vii) an interface device database module, comprising digitally-captured or patient-entered patient values, drug information, and dispensing-related information;
wherein the system utilizes information selected from the group consisting of prescription information, drug dispenser device information, patient self-assessment information, digitally captured physiological, psychological, lifestyle information, information of medications administered to the patient, environmental data information, and combinations thereof,
wherein the system captures such information before, during or after each drug dispensing and which is utilized by the drug specific diagnostic algorithm to decide if the separate or standalone drug dispenser device should dispense the drug or preclude dispensing and stay locked even in circumstances when the prescribed dose would have otherwise been allowed by the prescription, thereby preventing dose-mediated adverse events; and
wherein the drug specific diagnostic algorithm further utilizes symptom data obtained from the patient regarding the patient's symptoms and, based on the symptom data, decides if the separate or standalone drug dispenser device should dispense the drug or preclude dispensing and stay locked even in circumstances when the prescribed dose would have otherwise been allowed by the prescription, thereby preventing dose-mediated adverse events.
125. The method of claim 124, wherein the symptoms analyzed by the drug specific diagnostic algorithm are selected from the group consisting of pupil size, level of pain, stool and bowel movement information, respiratory rate, blood oxygen saturation, pulse, heart rhythm, blood pressure, gait, muscle spasms, and skin temperature.
126. The method of claim 124, wherein the drug cassette comprises an opioid.
127. The method of claim 124, wherein the drug specific dispensing algorithm automatically handshakes with the separate or standalone drug dispenser device and the one or more digital capture devices.
128. The method of claim 124, wherein the drug specific dispensing algorithm downloads data captured by the one or more digital capture devices to the interface device.
129. The method of claim 124, wherein the app checks a serial number of the separate or standalone drug dispenser device to ensure it is authorized to interface with the app.
130. The method of claim 124, wherein the app checks the expiration date of the drug.
131. The method of claim 124, wherein the app checks the storage temperature history to ensure the drug has been stored within a specific temperature range.
132. The method of claim 124, wherein the app checks the storage humidity history to ensure the drug has been stored within an authorized humidity range.
133. The method of claim 124, wherein the app retrieves drug information from the separate or standalone drug dispenser device.
134. The method of claim 124, wherein the app is designed to receive alerts of unauthorized attempts to open the separate or standalone drug dispenser device.
135. The method of claim 124, wherein the app stores a drug's prescription and dosing schedule.
136. The method of claim 124, wherein the app reminds the patient to take his/her medication and after a specific period of time alerts the integrated support center and/or authorized care givers that the patient has not taken his/her medication.
137. The method of claim 124, wherein the app is designed to automatically handshake with the patient's digital diagnostic, monitoring and/or tracking devices.
138. The method of claim 124, wherein the app presents drug specific patient self-assessment and/or data input screen(s).
139. The method of claim 124, wherein the app maintains a database of patient responses captured by self-assessment and/or data input screen(s) and digitally captured values.
140. The method of claim 124, wherein the interface device is a smart phone.
141. The method of claim 124, wherein the app allows the patient to click on a screen to automatically call the integrated support center.
142. The method of claim 124, wherein the app records all unsuccessful attempts to dispense a dose earlier than prescribed.
143. The method of claim 124, wherein the app has reporting routines that allow the patient to request certain reports created using the patient self-assessment, digital captured information, drug cassette information, and/or dosing information to ascertain if the drug is efficacious for the patient and the effect that dosing has on the patient's condition and/or symptoms.
144. The method of claim 124, wherein the app effectuates a handshake with the integrated support center's computers.
145. The method of claim 124, wherein the app downloads the patient's drug related dispensing information, comprising drug dispenser, patient self-assessment, or digitally captured information into the patient's records in the integrated support center's database.
146. The method of claim 124, wherein the app allows the patient to request specific drug related information stored in the app.
147. The method of claim 124, wherein the app allows the patient to request specific reports or information stored on the integrated support center's servers.
148. The method of claim 124, wherein the app allows the patient to correct responses entered in prior screens before dispensing the medication.
149. The method of claim 124, wherein the app contains a copy of or enables access to a patient app and drug dispenser operations training and troubleshooting manual.
150. The method of claim 124, wherein the app further comprises a GPS module to record the patient's location to ascertain where the patient is when the medication is dispensed.
151. The method of claim 124, wherein the drug dispenser device comprises an integrated drug cassette or a replaceable drug cassette.
152. The method of claim 127, wherein the drug specific dispensing algorithm prompts the patient self-assessment module to ask the patient one or more questions about his/her condition.
153. The drug dispensing system according to claim 124, wherein the drug dispenser device further comprises a replaceable drug cassette and wherein the app further comprises a security system to limit the ability to change the replaceable drug cassette to an authorized medical professional.
US16/858,451 2015-08-11 2020-04-24 Devices, system and method to control the delivery of oral medications to ensure they are efficacious, taken as prescribed, and to avoid unwanted side effects Abandoned US20200276088A1 (en)

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