fda_drug_adverse_events
ActiveTool of io.github.blackboxfoundry/livedatalink
declared in 1.0.0
FDA Adverse Event Reporting System (FAERS) reports for a specific drug. Each result describes a reported adverse reaction including patient demographics, reactions, outcome, and seriousness. Used for pharmacovigilance and post-market safety analysis.
Parameters schema
{
"type": "object",
"$schema": "http://json-schema.org/draft-07/schema#",
"required": [
"drug"
],
"properties": {
"drug": {
"type": "string",
"description": "Drug name (brand or generic) to query FAERS for. Example: 'Lipitor' or 'atorvastatin'."
},
"limit": {
"type": "number",
"description": "Maximum rows to return (default 25, max 100)."
},
"end_date": {
"type": "string",
"description": "Inclusive ISO date upper bound (YYYY-MM-DD)."
},
"reaction": {
"type": "string",
"description": "Optional MedDRA-preferred-term reaction filter (e.g. 'headache', 'nausea', 'liver injury')."
},
"start_date": {
"type": "string",
"description": "Inclusive ISO date lower bound (YYYY-MM-DD)."
},
"serious_only": {
"type": "boolean",
"description": "If true, only return serious adverse events (death, hospitalization, life-threatening, disability)."
}
},
"additionalProperties": false
}No endpoints wrapped at confidence ≥ 0.50.
Parent server
io.github.blackboxfoundry/livedatalink
https://github.com/blackboxfoundry/livedatalink
2/7 registries