Stimulated Reporting: The Impact of US Food and Drug Administration-Issued Alerts on the Adverse Event Reporting System (FAERS)

BACKGROUND: The US Food and Drug Administration (FDA) uses the Adverse Event Reporting System (FAERS) to support post-marketing safety surveillance programs. Currently, almost one million case reports are submitted to FAERS each year, making it a vast repository of drug safety information. Sometimes...

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Detalles Bibliográficos
Autores principales: Hoffman, Keith B., Demakas, Andrea R., Dimbil, Mo, Tatonetti, Nicholas P., Erdman, Colin B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2014
Materias:
Original Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206770/
https://www.ncbi.nlm.nih.gov/pubmed/25255848
http://dx.doi.org/10.1007/s40264-014-0225-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206770/
https://www.ncbi.nlm.nih.gov/pubmed/25255848
http://dx.doi.org/10.1007/s40264-014-0225-0

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