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ready FDA's Adverse Event Reporting System

Abbreviation:FAERS

General Information
The FDA Adverse Event Reporting System (FAERS) is a database that contains information on adverse event and medication error reports submitted to FDA.

Homepage https://www.fda.gov/drugs/surveillance/questions-and-answers-fdas-adverse-event-reporting-system-faers

Countries that developed this resource United States

Created in 2014

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Awaiting DOI assignment.


Record added: Oct. 14, 2020, 2:40 p.m.
Record updated: Oct. 14, 2020, 2:40 p.m. by The FAIRsharing Team.




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