FDA adverse events, drug approvals, recalls, CDC surveillance, hospital quality scores, and provider data — unified in one developer-friendly API. Stop juggling 5 government endpoints.
# Get all adverse events for Ozempic
curl https://api.myfitbyte.com/v1/drugs/adverse-events \
-H "Authorization: Bearer your_api_key" \
-d '{"drug": "ozempic", "year": 2026}'
# Response
{
"drug": {
"generic_name": "Semaglutide",
"brand_names": ["Ozempic", "Wegovy", "Rybelsus"]
},
"adverse_events": {
"total_reports": 34521,
"serious": 8203,
"top_reactions": ["nausea", "vomiting", "pancreatitis"],
"trend": "+12% vs last quarter"
},
"sources": ["fda_faers", "cdc_surveillance"]
}You could. But here's what you'd deal with:
FDA, CDC, CMS, NPI, NIH — each with different auth, query syntax, rate limits, and schemas. We unified them.
Search "Ozempic" and get results for semaglutide, all NDC codes, and every brand name variant. Across all sources.
FDA field "drugcharacterization: 1" becomes "role: suspect". No more decoding cryptic government field codes.
We cache 47M+ records in our database. No gov API rate limits, no downtime, no quarterly lag.
Get notified the moment a drug is recalled, a new adverse event spike is detected, or approval status changes.
Ground your health AI in real data. MCP server available for LLM integrations. No hallucinated drug interactions.
Join the waitlist and be first to get an API key when we launch.