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FDA ADE reports for Epoetin Alfa

ade_epoetin_alfa_adverse_events

ade en 2026-07-22

Epoetin Alfa 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. Epoetin Alfa is a active ingredient.

Total reports

Epoetin Alfa: 13

Reports by species (top entries)

  • Cat 7
  • Dog 6

Top reported reactions (VEDDRA terms, top entries)

  • Anaemia NOS 4
  • Death by euthanasia 4
  • Anorexia 3
  • Lethargy (see also Central nervous system depression in 'Neurological') 3
  • Leucocytosis NOS 3
  • Pale mucous membrane 3
  • Weight loss 3
  • Behavioural disorder NOS 2
  • Decreased haematocrit 2
  • Decreased haemoglobin 2

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b30.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).