FAERS

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

High-level description of data source(s): The Federal Adverse Event Reporting System (FAERS) provides information on adverse events reported to the US FDA by the pharmaceutical industry, healthcare providers, and consumers. The adverse events are self-reported claims as being related to drugs and biologics, but the US FDA makes not attempt to determine causality, and so, the FAERS data should not be used as a measure of drug or biologic safety.

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