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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.

Source: OpenFDATest
FieldValue
Publisher
Modified
2013-08-16
Release Date
2013-08-16
Homepage URL
Identifier
c696c4f7-6de9-45db-988a-7195c2ade1d0
License
License Not Specified
Contact Name
CDER OSE Tracking
Contact Email
Public Access Level
Public
Harvested from OpenFDATest
Harvest Source TitleOpenFDATest
Harvest Source URIhttps://open.fda.gov/data.json
Last Harvest PerformedThu, 01/10/2019 - 00:04