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

    Metadata Updated: July 11, 2025

    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.

    Access & Use Information

    Public: This dataset is intended for public access and use. License: See this page for license information.

    Downloads & Resources

    Dates

    Metadata Created Date November 10, 2020
    Metadata Updated Date July 11, 2025

    Metadata Source

    Harvested from Healthdata.gov

    Other Data Resources

    Additional Metadata

    Resource Type Dataset
    Metadata Created Date November 10, 2020
    Metadata Updated Date July 11, 2025
    Publisher U.S. Food and Drug Administration
    Maintainer
    Identifier c696c4f7-6de9-45db-988a-7195c2ade1d0
    Data First Published 2021-02-25
    Data Last Modified 2013-08-16
    Category FDA
    Public Access Level public
    Bureau Code 009:10
    Metadata Context https://project-open-data.cio.gov/v1.1/schema/catalog.jsonld
    Metadata Catalog ID https://healthdata.gov/data.json
    Schema Version https://project-open-data.cio.gov/v1.1/schema
    Catalog Describedby https://project-open-data.cio.gov/v1.1/schema/catalog.json
    Harvest Object Id c5e67e69-b12d-4906-aae8-26d901300e56
    Harvest Source Id 651e43b2-321c-4e4c-b86a-835cfc342cb0
    Harvest Source Title Healthdata.gov
    Homepage URL http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/AdverseDrugEffects/ucm082193.htm
    License http://opendefinition.org/licenses/odc-odbl/
    Program Code 009:002
    Source Datajson Identifier True
    Source Hash 73c2f5598ff518091a678ec27ddc0272cfbd1600772b8ad41fb189307f2a877e
    Source Schema Version 1.1

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