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URL: http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/AdverseDrugEffects/
Proper Citation: FDA Adverse Event Reporting System Data (RRID:SCR_013718)
Description: Database that contains information on adverse event and medication error reports submitted to FDA. The database is designed to support the FDA's post-marketing safety surveillance program for drug and therapeutic biologic products.
Abbreviations: FAERS
Synonyms: Adverse Event Reporting System Data, Adverse Event Reporting System
Keywords: adverse event, database, medication error reports
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