FDA Adverse Event Reporting System (FAERS): Latest Quartely Data Files

Description

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.

Resources

Name Format Description Link
57 ucm082193.htm http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/AdverseDrugEffects/ucm082193.htm

Tags

  • drugs
  • cder
  • reporting-system
  • faers
  • adverse-event

Topics

Categories