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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Detalles Bibliográficos
Autores principales: Tang, Huaxiu, Solti, Imre, Kirkendall, Eric, Zhai, Haijun, Lingren, Todd, Meller, Jaroslaw, Ni, Yizhao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5467704/
https://www.ncbi.nlm.nih.gov/pubmed/28634427
http://dx.doi.org/10.1177/1178222617713018

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5467704/
https://www.ncbi.nlm.nih.gov/pubmed/28634427
http://dx.doi.org/10.1177/1178222617713018

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