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FDA ADE reports for Toceranib

ade_toceranib_phosphate_adverse_events

ade en 2026-07-22

Toceranib โ€” 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. Toceranib is a active ingredient.

Total reports

Toceranib: 1262

Reports by species (top entries)

  • Dog 1058
  • Cat 99
  • Human 27
  • Other Rodents 1
  • Rabbit 1

Top reported reactions (VEDDRA terms, top entries)

  • Diarrhoea 229
  • Vomiting 211
  • Anorexia 174
  • Anaemia NOS 114
  • Death by euthanasia 108
  • Neutropenia 105
  • Lack of efficacy - NOS 102
  • Lameness 99
  • Weight loss 92
  • Lethargy (see also Central nervous system depression in 'Neurological') 87

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b10.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).