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An Evaluation of “Drug Ineffective” Postmarketing Reports in Drug Safety Surveillance

INTRODUCTION: The most commonly reported adverse event, based on frequency of Medical Dictionary for Regulatory Activities (MedDRA) preferred terms (PTs), in the US FDA Adverse Event Reporting System (FAERS) database is “drug ineffective” (DI). This study aimed to describe the DI reports and provide...

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Detalhes bibliográficos
Publicado no:Drugs Real World Outcomes
Main Authors: Misu, Takashi, Kortepeter, Cindy M., Muñoz, Monica A., Wu, Eileen, Dal Pan, Gerald J.
Formato: Artigo
Idioma:Inglês
Publicado em: Springer International Publishing 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5984607/
https://ncbi.nlm.nih.gov/pubmed/29476420
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40801-018-0131-3
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