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.
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Complete Metadata
| @type | dcat:Dataset |
|---|---|
| accessLevel | public |
| bureauCode |
[ "009:10" ] |
| contactPoint |
{ "fn": "CDER OSE Tracking", "@type": "vcard:Contact", "hasEmail": "mailto:cderosetracking@fda.hhs.gov" } |
| description | 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. |
| distribution |
[ { "@type": "dcat:Distribution", "mediaType": "application/zip", "downloadURL": "http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/AdverseDrugEffects/ucm082193.htm" } ] |
| identifier | c696c4f7-6de9-45db-988a-7195c2ade1d0 |
| issued | 2021-02-25 |
| keyword |
[ "adverse event", "cder", "drugs", "faers", "reporting system" ] |
| landingPage | http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/AdverseDrugEffects/ucm082193.htm |
| license | http://opendefinition.org/licenses/odc-odbl/ |
| modified | 2013-08-16 |
| programCode |
[ "009:002" ] |
| publisher |
{ "name": "U.S. Food and Drug Administration", "@type": "org:Organization" } |
| theme |
[ "FDA" ] |
| title | FDA Adverse Event Reporting System (FAERS): Latest Quartely Data Files |
