The impact of the boxed warning on the duration of use for depot medroxprogesterone acetate

Author:

Eworuke Efe1ORCID,Lee Joo-Yeon2,Soule Lisa3,Popat Vaishali4,Moeny David G.1

Affiliation:

1. Division of Epidemiology II, Office of Pharmacovigilance and Epidemiology, Office of Surveillance and Epidemiology; Center for Drug Evaluation and Research, Food and Drug Administration; Silver Spring MA USA

2. Division of Biometrics VII, Office of Biostatistics; Center for Drug Evaluation and Research, Food and Drug Administration; Silver Spring MA USA

3. Division of Bone, Reproductive, and Urologic Products; Office of New Drugs, Center for Drug Evaluation and Research, Food and Drug Administration; Silver Spring MA USA

4. Office of New Drugs, Immediate Office; Center for Drug Evaluation and Research, Food and Drug Administration; Silver Spring MA USA

Publisher

Wiley

Subject

Pharmacology (medical),Epidemiology

Reference19 articles.

1. Services USHaH Depo-Provera (NDA 020246) Label and Approval History Administration FaD Silver Spring U.S. Department of Health and Human Services

2. Services USHaH Depo-Sub Q Provera (NDA 021583) Label and Approval History Administration FaD Silver Spring U.S. Department of Health and Human Services

3. Magnitude and variability of sequential estradiol and progesterone concentrations in women using depot medroxyprogesterone acetate for contraception;Clark;Fertil Steril,2001

4. Effects of hormonal contraception on bone mineral density after 24 months of use;Berenson;Obstet Gynecol

5. A prospective, controlled study of the effects of hormonal contraception on bone mineral density;Berenson;Obstet Gynecol,2001

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