FDA's Adverse Event Reporting System

Other names: FAERS, faers

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

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

Licence:
Name: FAERS disclaimer
URL: https://fis.fda.gov/sense/app/d10be6bb-494e-4cd2-82e4-0135608ddc13/sheet/7a47a261-d58b-4203-a8aa-6d3021737452/state/analysis

Publications:

Tags:

drug report safety sciences surgery allergy, clinical immunology and immunotherapeutics preclinical and clinical studies public health and epidemiology rare diseases

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