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FDA ADE reports for Ractopamine

ade_ractopamine_adverse_events

ade en 2026-07-22

Ractopamine 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. Ractopamine is a active ingredient.

Total reports

Ractopamine: 69

Reports by species (top entries)

  • Pig 25
  • Dog 17
  • Cattle 15
  • Horse 3
  • Human 2
  • Turkey 2

Top reported reactions (VEDDRA terms, top entries)

  • Death 16
  • Lethargy (see also Central nervous system depression in 'Neurological') 13
  • Behavioural disorder NOS 7
  • Pneumonia 7
  • Unclassifiable adverse event 7
  • Death by euthanasia 6
  • Lameness 6
  • Tachycardia 6
  • Anorexia 4
  • Increased heart rate 4

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b12.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).