Leveraging Food and Drug Administration Adverse Event Reports for the Automated Monitoring of Electronic Health Records in a Pediatric Hospital

The objective of this study was to determine whether the Food and Drug Administration’s Adverse Event Reporting System (FAERS) data set could serve as the basis of automated electronic health record (EHR) monitoring for the adverse drug reaction (ADR) subset of adverse drug events. We retrospectivel...

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Vydáno v:Biomed Inform Insights
Hlavní autoři: Tang, Huaxiu, Solti, Imre, Kirkendall, Eric, Zhai, Haijun, Lingren, Todd, Meller, Jaroslaw, Ni, Yizhao
Médium: Artigo
Jazyk:Inglês
Vydáno: SAGE Publications 2017
Témata:
Original Research
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5467704/
https://ncbi.nlm.nih.gov/pubmed/28634427
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1178222617713018
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