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FDA ADE reports for Verdinexor

ade_verdinexor_adverse_events

ade en 2026-07-22

Verdinexor 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. Verdinexor is a active ingredient.

Total reports

Verdinexor: 422

Reports by species (top entries)

  • Dog 419
  • Human 3

Top reported reactions (VEDDRA terms, top entries)

  • Vomiting 112
  • Death by euthanasia 110
  • Weight loss 94
  • Diarrhoea 69
  • Lack of efficacy - NOS 68
  • Elevated alanine aminotransferase (ALT) 65
  • Decreased appetite 61
  • Thrombocytopenia 56
  • Anorexia 50
  • Death 46

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b15.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).