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FDA ADE reports for Poloxalene

ade_poloxalene_adverse_events

ade en 2026-07-22

Poloxalene 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. Poloxalene is a active ingredient.

Total reports

Poloxalene: 33

Reports by species (top entries)

  • Cattle 16
  • Human 3
  • Goat 2
  • Horse 2
  • Sheep 1

Top reported reactions (VEDDRA terms, top entries)

  • Death 6
  • Lack of efficacy - NOS 5
  • Accidental exposure 4
  • Unclassifiable adverse event 4
  • Death by euthanasia 3
  • Depression 3
  • Ruminal bloat 3
  • Color, Abnormal 2
  • Diarrhoea 2
  • No sign 2

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b26.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).