The Weber Effect and the United States Food and Drug Administration’s Adverse Event Reporting System (FAERS): Analysis of Sixty-Two Drugs Approved from 2006 to 2010

BACKGROUND: The United States Food and Drug Administration’s (FDA) Adverse Event Reporting System (FAERS) consists of adverse event (AE) reports linked to approved drugs. The database is widely used to support post-marketing safety surveillance programs. Sometimes cited as a limitation to the useful...

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Detalles Bibliográficos
Autores principales: Hoffman, Keith B., Dimbil, Mo, Erdman, Colin B., Tatonetti, Nicholas P., Overstreet, Brian M.
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/PMC3975089/
https://www.ncbi.nlm.nih.gov/pubmed/24643967
http://dx.doi.org/10.1007/s40264-014-0150-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975089/
https://www.ncbi.nlm.nih.gov/pubmed/24643967
http://dx.doi.org/10.1007/s40264-014-0150-2

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