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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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Dettagli Bibliografici
Pubblicato in:Biomed Inform Insights
Autori principali: Tang, Huaxiu, Solti, Imre, Kirkendall, Eric, Zhai, Haijun, Lingren, Todd, Meller, Jaroslaw, Ni, Yizhao
Natura: Artigo
Lingua:Inglês
Pubblicazione: SAGE Publications 2017
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Accesso online: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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