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

http://www.fda.gov/Drugs/GuidanceComplianceRegu...ZIP
ucm082193.htm

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Dates

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

Metadata Source

Data.json Data.json Metadata
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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	admin
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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