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FDA ADE reports for Allopurinol

ade_allopurinol_adverse_events

ade en 2026-07-22

Allopurinol 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. Allopurinol is a active ingredient.

Total reports

Allopurinol: 17

Reports by species (top entries)

  • Dog 12
  • Human 4
  • Other Birds 1

Top reported reactions (VEDDRA terms, top entries)

  • Death 2
  • Elevated serum alkaline phosphatase (SAP) 2
  • Emesis 2
  • Lack of efficacy - NOS 2
  • Leucocytosis NOS 2
  • Reluctant to move 2
  • Abnormal posture NOS 1
  • Accidental exposure 1
  • Application site blister 1
  • Application site burning sensation 1

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b32.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).