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CO5280075A1 - DROSPIRENONE FOR HORMONE REPLACEMENT THERAPY - Google Patents

DROSPIRENONE FOR HORMONE REPLACEMENT THERAPY

Info

Publication number
CO5280075A1
CO5280075A1 CO01003045A CO01003045A CO5280075A1 CO 5280075 A1 CO5280075 A1 CO 5280075A1 CO 01003045 A CO01003045 A CO 01003045A CO 01003045 A CO01003045 A CO 01003045A CO 5280075 A1 CO5280075 A1 CO 5280075A1
Authority
CO
Colombia
Prior art keywords
estrogen
active agent
drospirenone
carbolactone
preg
Prior art date
Application number
CO01003045A
Other languages
Spanish (es)
Inventor
Wolfgang Heil
Jurgen Hilmann
Ralph Lipp
Rolf Schurmann
Original Assignee
Bayer Schering Pharma Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bayer Schering Pharma Ag filed Critical Bayer Schering Pharma Ag
Publication of CO5280075A1 publication Critical patent/CO5280075A1/en

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Una composición farmacéutica que comprendecomo un primer agente activo, un estrógeno (o derivado natural o sintético del mismo) en cantidades suficientes para tratar enfermedades, desórdenes y síntomas asociados con niveles endógenos deficientes de estrógeno en mujeres, y como un segundo agente activo, 6ß, 7ß, 15ß, 16ß-dimetilen-3-oxo-17a-preg-4-eno-27,17-carbolactona (drospirenona) en cantidades suficientes para proteger el endometrio de los efectos adversos del estrógeno, conjuntamente con un excipiente o portador farmacéuticamente aceptable. Una composición farmacéutica que comprende estradiol como un primer agente activo en cantidades que corresponden a una dosis diaria de 1 a 3 mg para tratar enfermedades, desórdenes y síntomas asociados con niveles endógenos deficientes de estrógeno en mujeres, y como un segundo agente activo 6ß, 7ß, 15ß, 16ß-dimetilen-3-oxo-17a-preg-4-eno-27,17-carbolactona (drospirerona) en cantidades suficientes que corresponden a una dosis diaria de 1 a 3,5 mg para proteger el endometrio de los efectos adversos del estrógeno, junto con un excipiente o portador farrnacéuticamente aceptable.Una preparación farmacéutica multi-fásica que consiste en un número de unidades de dosificación diarias separadamente envasadas e individualmente removibles dispuestas dentro de una unidad de envase destinadas a administración oral durante un periodo de al menos 21 días donde dichas unidades de dosificación diarias comprenden una combinación de estradiol en una cantidad en el rango de desde aproximadamente 0,1 a 5 mg y drospirenona en el rango de desde aproximadamente 0,25 a 6 mg.A pharmaceutical composition comprising as a first active agent, an estrogen (or natural or synthetic derivative thereof) in amounts sufficient to treat diseases, disorders and symptoms associated with endogenous estrogen deficient levels in women, and as a second active agent, 6β, 7ß, 15ß, 16ß-dimethylene-3-oxo-17a-preg-4-eno-27.17-carbolactone (drospirenone) in amounts sufficient to protect the endometrium from the adverse effects of estrogen, together with a pharmaceutically acceptable carrier or excipient . A pharmaceutical composition comprising estradiol as a first active agent in amounts corresponding to a daily dose of 1 to 3 mg to treat diseases, disorders and symptoms associated with endogenous estrogen deficient levels in women, and as a second active agent 6ß, 7ß , 15ß, 16ß-dimethylene-3-oxo-17a-preg-4-eno-27.17-carbolactone (drospirerona) in sufficient amounts corresponding to a daily dose of 1 to 3.5 mg to protect the endometrium from effects adverse effects of the estrogen, together with a pharmaceutically acceptable carrier or excipient. A multi-phase pharmaceutical preparation consisting of a number of separately dosed and individually removable daily dosage units disposed within a container unit intended for oral administration during a period of at least minus 21 days where said daily dosage units comprise a combination of estradiol in an amount in the range of from apr approximately 0.1 to 5 mg and drospirenone in the range of from about 0.25 to 6 mg.

CO01003045A 2000-01-18 2001-01-17 DROSPIRENONE FOR HORMONE REPLACEMENT THERAPY CO5280075A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP00200183 2000-01-18

Publications (1)

Publication Number Publication Date
CO5280075A1 true CO5280075A1 (en) 2003-05-30

Family

ID=38170612

Family Applications (1)

Application Number Title Priority Date Filing Date
CO01003045A CO5280075A1 (en) 2000-01-18 2001-01-17 DROSPIRENONE FOR HORMONE REPLACEMENT THERAPY

Country Status (7)

Country Link
AR (1) AR035633A1 (en)
CO (1) CO5280075A1 (en)
HR (1) HRP20070360B1 (en)
JO (1) JO2334B1 (en)
PE (1) PE20011051A1 (en)
SA (1) SA01210754B1 (en)
UA (2) UA81388C2 (en)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4426601A1 (en) * 1994-07-27 1996-02-01 Schering Ag Use of a combination product containing a competitive progesterone antagonist and a progestogen for the manufacture of a medicament for the treatment of endometriosis or Leiomyomata uteri
DE19654609A1 (en) * 1996-12-20 1998-06-25 Schering Ag Therapeutic progestogens for the treatment of premenstrual dysphoric disorder
RS50262B2 (en) * 1999-08-31 2018-10-31 Bayer Pharma AG PHARMACEUTICAL COMBINATION OF ETHINYLESTRADIOL AND DROSPIRENONE FOR ADMINISTRATION AS CONTRACEPTIVE

Also Published As

Publication number Publication date
UA81388C2 (en) 2008-01-10
UA89180C2 (en) 2010-01-11
HRP20070360A2 (en) 2008-12-31
AR035633A1 (en) 2004-06-23
SA01210754B1 (en) 2007-02-17
JO2334B1 (en) 2006-06-28
PE20011051A1 (en) 2001-10-17
HRP20070360B1 (en) 2014-11-21

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Legal Events

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