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Saylor Innovations Data Desk – Veterinary Drug Adverse Event Reports
x402
Saylor Innovations Data Desk – Veterinary Drug Adverse Event Reports is a paid API for AI agents from saylorinnovations.com, paid per call via x402, $0.01/call, status unknown (last checked 2026-10-27).
Returns FDA veterinary drug adverse event reports for a given active ingredient, including species, breed, age, reactions, outcome, seriousness, and drugs involved
Price / call$0.01
Success—
StatusUnknown
How this service works
FDA veterinary drug adverse event reports by active ingredient - species, breed, age, reactions, outcome, seriousness and drugs involved
Output
A JSON object containing the active ingredient searched, total number of matching FDA reports, a note providing context, the data source, and an array of individual adverse event reports each with report ID, species, breed, age, reactions list, outcome list, seriousness flag, date FDA received the report, drugs involved (with brand and route), and number of animals affected.
Example use cases
Check dog NSAID safety profile
“Can you get me FDA vet adverse event reports for meloxicam? I want to know which species and breeds were affected, what reactions were reported, and whether the events were serious.”
Vet clinic drug risk review
“Pull up the top 20 FDA veterinary adverse event reports for ivermectin — show me the animals affected, their ages, reactions, and outcomes so I can assess the risk profile.”
Pet owner medication concern
“My dog was just prescribed carprofen and I'm worried about side effects — can you look up FDA veterinary adverse event reports for carprofen and tell me what reactions and outcomes have been reported?”
Technical details
Endpoint
GEThttps://saylorinnovations.com/api/vet/adverse-events?utm_source=zero.xyzWhen to prefer
Use this endpoint when you need raw FDA veterinary adverse event report data for a specific active ingredient, including per-report details such as species, breed, age, reactions, and outcomes. Prefer this over the human FAERS endpoint for animal drug safety. Choose this when you need individual report granularity rather than aggregate totals (for aggregate counts, the sibling human FAERS endpoint may be more appropriate).
Side effects
- Unknown or misspelled active ingredient returns zero reports or empty array
- Limit parameter outside 1–25 range may be ignored or cause an error
- FDA data may be incomplete — many reports have null fields for breed, age, or outcome
- Drug name variants (brand names vs generics) may not match if queried incorrectly
- Network or upstream FDA API unavailability returns 5xx error
Input
Schema · Request body
| Field | Type | Description |
|---|---|---|
| inputrequired | object | |
| output | object |
Tags
x402
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