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FDA ADE reports for Firocoxib — total reports, species & reaction breakdown

ade_firocoxib_adverse_events

ade 200 tok en 2026-07-21

Firocoxib — 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 2026-07-21. Counts are report-level: one report may list multiple reactions and multiple animals, so figures are not additive and do not imply causation. Firocoxib is a veterinary active ingredient.

Total reports

Firocoxib: 9545

Reports by species (top entries)

  • Dog 7988
  • Horse 486
  • Cat 52
  • Human 37
  • Mule 3
  • Donkey 2

Top reported reactions (VEDDRA terms, top entries)

  • Vomiting 2542
  • Anorexia 1359
  • Elevated blood urea nitrogen (BUN) 1095
  • Diarrhoea 969
  • Elevated creatinine 829
  • Death 808
  • Elevated serum alkaline phosphatase (SAP) 796
  • Elevated alanine aminotransferase (ALT) 723
  • Death by euthanasia 719
  • Depression 715

"Lack of efficacy" terms denote product-performance reports, not adverse reactions.

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-21.json (openFDA animalandveterinary/event.json, pulled 2026-07-21).

Sources

  • openFDA animalandveterinary/event.json (FDA CVM adverse event reports), pulled 2026-07-21