{"@type": "dcat:Dataset", "accessLevel": "public", "bureauCode": ["009:10"], "contactPoint": {"@type": "vcard:Contact", "fn": "CDER OSE Tracking", "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", "downloadURL": "http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Surveillance/AdverseDrugEffects/ucm082193.htm", "mediaType": "application/zip"}], "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": {"@type": "org:Organization", "name": "U.S. Food and Drug Administration"}, "theme": ["FDA"], "title": "FDA Adverse Event Reporting System (FAERS): Latest Quartely Data Files"}