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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Detalles Bibliográficos
Autores principales: Misu, Takashi, Kortepeter, Cindy M., Muñoz, Monica A., Wu, Eileen, Dal Pan, Gerald J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Original Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984607/
https://www.ncbi.nlm.nih.gov/pubmed/29476420
http://dx.doi.org/10.1007/s40801-018-0131-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984607/
https://www.ncbi.nlm.nih.gov/pubmed/29476420
http://dx.doi.org/10.1007/s40801-018-0131-3

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