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FDA ADE reports for Amprolium

ade_amprolium_adverse_events

ade en 2026-07-22

Amprolium 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. Amprolium is a active ingredient.

Total reports

Amprolium: 303

Reports by species (top entries)

  • Cattle 90
  • Human 30
  • Goat 9
  • Dog 8
  • Chicken 7
  • Sheep 6

Top reported reactions (VEDDRA terms, top entries)

  • Appearance, Abnormal 73
  • Death 49
  • Lack of efficacy (protozoa) - Coccidia 43
  • Contamination, Particulate Matter 34
  • Accidental exposure 30
  • Potency, Low 19
  • Diarrhoea 17
  • Unclassifiable adverse event 17
  • Bloody diarrhoea 15
  • Product defect NOS 10

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b16.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).