Automatically Recognizing Medication and Adverse Event Information From Food and Drug Administration’s Adverse Event Reporting System Narratives

BACKGROUND: The Food and Drug Administration’s (FDA) Adverse Event Reporting System (FAERS) is a repository of spontaneously-reported adverse drug events (ADEs) for FDA-approved prescription drugs. FAERS reports include both structured reports and unstructured narratives. The narratives often includ...

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Detalles Bibliográficos
Autores principales: Polepalli Ramesh, Balaji, Belknap, Steven M, Li, Zuofeng, Frid, Nadya, West, Dennis P, Yu, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Gunther Eysenbach 2014
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4288072/
https://www.ncbi.nlm.nih.gov/pubmed/25600332
http://dx.doi.org/10.2196/medinform.3022

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4288072/
https://www.ncbi.nlm.nih.gov/pubmed/25600332
http://dx.doi.org/10.2196/medinform.3022

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