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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Bibliographische Detailangaben
Veröffentlicht in:JMIR Med Inform
Hauptverfasser: Polepalli Ramesh, Balaji, Belknap, Steven M, Li, Zuofeng, Frid, Nadya, West, Dennis P, Yu, Hong
Format: Artigo
Sprache:Inglês
Veröffentlicht: Gunther Eysenbach 2014
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Original Paper
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4288072/
https://ncbi.nlm.nih.gov/pubmed/25600332
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2196/medinform.3022
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