Literature DB >> 24508124

Ulipristal acetate for emergency contraception: postmarketing experience after use by more than 1 million women.

Delphine P Levy1, Martine Jager1, Nathalie Kapp2, Jean-Louis Abitbol1.   

Abstract

OBJECTIVE: To describe the safety of ulipristal acetate in emergency contraception. STUDY
DESIGN: Postmarketing pharmacovigilance data collection.
RESULTS: A total of 553 women experienced 1049 adverse drug reactions. The most frequent (n,%) were pregnancies (282, 6.8%); nausea, abdominal pain and vomiting (139, 13.3%); headache, dizziness (67, 6.4%); and metrorrhagia, menses delay and breast symptoms (84, 8.0%). Including data from clinical trials, 376 pregnancies have been reported in total, 232 (62%) with a known outcome: 28 live births (29 newborns), 34 miscarriages, 151 induced abortions, 4 ectopics and 15 which are ongoing.
CONCLUSIONS: No safety concern emerges from a sizable database of reported adverse reactions following ulipristal acetate exposure among varying ethnicities and regions. Postapproval data confirm the safety profile described during the clinical trials. IMPLICATIONS: Use of ulipristal acetate for emergency contraception in a variety of settings and among diverse populations indicate that it is safe and without unexpected or serious adverse events.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Adverse drug reactions; Drug safety; Ella; EllaOne; Pharmacovigilence; Safety of EC; Safety profile of ella

Mesh:

Substances:

Year:  2014        PMID: 24508124     DOI: 10.1016/j.contraception.2014.01.003

Source DB:  PubMed          Journal:  Contraception        ISSN: 0010-7824            Impact factor:   3.375


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