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

Metadata Updated: November 10, 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: See this page for license information.

Downloads & Resources

Dates

Metadata Created Date November 10, 2020
Metadata Updated Date November 10, 2020

Metadata Source

Harvested from Healthdata.gov

Additional Metadata

Resource Type Dataset
Metadata Created Date November 10, 2020
Metadata Updated Date November 10, 2020
Publisher Department of Health & Human Services
Unique Identifier Unknown
Maintainer
Identifier 9f1ba341-723c-480b-887e-e72f043d4abe
Data First Published 2015-03-31
Data Last Modified 2016-04-05
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
Homepage URL https://healthdata.gov/dataset/fda-adverse-event-reporting-system-faers-latest-quartely-data-files-0
License https://opendatacommons.org/licenses/odbl/1.0/
Program Code 009:002
Source Datajson Identifier True
Source Hash 95d6b7b876f4616310a9c4942e0c7a9690c0a976
Source Schema Version 1.1

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