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Am J Obstet Gynecol ; 210(1): 47.e1-7, 2014 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-24200163

RESUMO

OBJECTIVE: The purpose of this study was to evaluate the quality of compounded 17-hydroxyprogesterone caproate (17-OHPC). STUDY DESIGN: Compounded 17-OHPC that was obtained from 15 compounding pharmacies throughout the United States was analyzed for potency, impurities, sterility, and pyrogen status. RESULTS: Eighteen samples were supplied by 15 compounding pharmacies. The concentration of 17-OHPC in all samples was within the specification limits, and all tested samples passed sterility and pyrogen testing. Only 1 of 18 samples was out of specification limits for impurities. CONCLUSION: Compounded 17-OHPC that was obtained from 15 pharmacies throughout the United States did not raise safety concerns when assessed for potency, sterility, pyrogen status, or impurities.


Assuntos
Composição de Medicamentos/normas , Hidroxiprogesteronas/normas , Caproato de 17 alfa-Hidroxiprogesterona , Humanos , Hidroxiprogesteronas/análise , Pirogênios , Garantia da Qualidade dos Cuidados de Saúde , Controle de Qualidade , Estados Unidos
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