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• W2113753800 startingPage "e10" @default.
• W2113753800 abstract "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 include essential information for evaluation of the severity, causality, and description of ADEs that are not present in the structured data. The timely identification of unknown toxicities of prescription drugs is an important, unsolved problem." @default.
• W2113753800 created "2016-06-24" @default.
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• W2113753800 creator A5067763072 @default.
• W2113753800 date "2014-06-27" @default.
• W2113753800 modified "2023-09-25" @default.
• W2113753800 title "Automatically Recognizing Medication and Adverse Event Information From Food and Drug Administration’s Adverse Event Reporting System Narratives" @default.
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• W2113753800 doi "https://doi.org/10.2196/medinform.3022" @default.
• W2113753800 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4288072" @default.
• W2113753800 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25600332" @default.
• W2113753800 hasPublicationYear "2014" @default.
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