FDA Adverse Event Reporting System (FAERS): Latest Quartely Data Files
The FDA Adverse Event Reporting System (FAERS) is a 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.
Complete Metadata
| bureauCode |
[ "009:10" ] |
|---|---|
| identifier | c696c4f7-6de9-45db-988a-7195c2ade1d0 |
| issued | 2021-02-25 |
| landingPage | http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/AdverseDrugEffects/ucm082193.htm |
| programCode |
[ "009:002" ] |
| theme |
[ "FDA" ] |
