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 |
