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

ade_robenacoxib_adverse_events

ade 200 tok en 2026-07-21

Robenacoxib — 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. Robenacoxib is a veterinary active ingredient.

Total reports

Robenacoxib: 3654

Reports by species (top entries)

  • Cat 3191
  • Dog 110
  • Human 7
  • Ferret 2
  • Other Birds 2
  • Rabbit 1

Top reported reactions (VEDDRA terms, top entries)

  • Not eating 409
  • Lethargy (see also Central nervous system depression in 'Neurological') 407
  • Lack of efficacy - NOS 321
  • Anorexia 310
  • Fever 307
  • Behavioural disorder NOS 296
  • Vomiting 293
  • Death by euthanasia 290
  • Other abnormal test result NOS 275
  • Lethargy (see also Central nervous system depression in Neurological) 250

"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