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

Metadata Updated: February 26, 2020

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: No license information was provided. If this work was prepared by an officer or employee of the United States government as part of that person's official duties it is considered a U.S. Government Work.

Downloads & Resources

Dates

Metadata Created Date August 20, 2018
Metadata Updated Date February 26, 2020

Metadata Source

Harvested from Healthdata.gov

Additional Metadata

Resource Type Dataset
Metadata Created Date August 20, 2018
Metadata Updated Date February 26, 2020
Publisher U.S. Food and Drug Administration
Unique Identifier c696c4f7-6de9-45db-988a-7195c2ade1d0
Maintainer
CDER OSE Tracking
Maintainer Email
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 35f9b156-eb23-4ce1-bc88-681239d50d8a
Harvest Source Id 15c538b5-31a0-474e-8ba5-c85ee421cb4d
Harvest Source Title Healthdata.gov
Data First Published 2013-08-16
Homepage URL http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/AdverseDrugEffects/ucm082193.htm
Data Last Modified 2013-08-16
Program Code 009:002
Source Datajson Identifier True
Source Hash a4b07e8d95af90686dd06cb274bbc2c60baef02c
Source Schema Version 1.1

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