FDA ADE reports for Decoquinate

ade_decoquinate_adverse_events

ade en 2026-07-22

Decoquinate — FDA Animal & Veterinary Adverse Event (ADE) Reports

Source: openFDA animalandveterinary/event.json, the FDA Center for Veterinary Medicine (CVM) adverse event report database. Data pulled 2026-07-22. Counts are report-level: one report may list multiple reactions and multiple animals, so figures are not additive and do not imply causation. Decoquinate is a active ingredient.

Total reports

Decoquinate: 159

Reports by species (top entries)

Cattle 102
Goat 7
Sheep 7
Chicken 4
Dog 3
Horse 3

Top reported reactions (VEDDRA terms, top entries)

Lack of efficacy (protozoa) - Coccidia 41
INEFFECTIVE, COCCIDIA 32
Death 31
No sign 21
Hard, clumping 18
Lack of efficacy - NOS 17
Device Defective NOS 8
Overdose 5
Seal, Abnormal 5
Sudden death 4

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b19.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

FDA ADE reports for Decoquinate (active ingredient) — total reports, species & reaction breakdown

Source document: FDA FAERS / openFDA Animal & Veterinary Event Reports

US FDA Center for Veterinary Medicine (openFDA animal & veterinary event database)retrieved 2026-07-22

Verification file: pdf-raw/ade/ade_active_ingredients_2026-07-22_b19.json

Link points to the issuing authority's site; a direct document link is still being verified.

Machine access

AI agents: this page mirrors GET /api/v1/llm_context?topic=ade_decoquinate_adverse_events (max 500 tokens, whitelisted). Rate limit 60 req/min for recognized AI crawlers.

Raw JSON ↗ llm.txt OpenAPI