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.

Data and Resources

Field Value
accessLevel public
bureauCode {009:10}
catalog_@context https://project-open-data.cio.gov/v1.1/schema/catalog.jsonld
catalog_@id https://healthdata.gov/data.json
catalog_conformsTo https://project-open-data.cio.gov/v1.1/schema
catalog_describedBy https://project-open-data.cio.gov/v1.1/schema/catalog.json
identifier c696c4f7-6de9-45db-988a-7195c2ade1d0
issued 2021-02-25
landingPage http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/AdverseDrugEffects/ucm082193.htm
license http://opendefinition.org/licenses/odc-odbl/
modified 2013-08-16
programCode {009:002}
publisher U.S. Food and Drug Administration
resource-type Dataset
source_datajson_identifier true
source_hash 9451a0b4d21ca7dca3440acf2416cef52cd33cca
source_schema_version 1.1
Groups
  • AmeriGEOSS
  • National Provider
  • North America
Tags
  • adverse-event
  • amerigeo
  • amerigeoss
  • cder
  • ckan
  • drugs
  • faers
  • geo
  • geoss
  • national
  • north-america
  • reporting-system
  • united-states
isopen False
license_id other-license-specified
license_title other-license-specified
maintainer CDER OSE Tracking
maintainer_email cderosetracking@fda.hhs.gov
metadata_created 2025-11-22T14:17:21.852605
metadata_modified 2025-11-22T14:17:21.852608
notes 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.
num_resources 1
num_tags 13
title FDA Adverse Event Reporting System (FAERS): Latest Quartely Data Files