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FDA ADE reports for Hetastarch

ade_hetastarch_adverse_events

ade en 2026-07-22

Hetastarch 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. Hetastarch is a active ingredient.

Total reports

Hetastarch: 78

Reports by species (top entries)

  • Dog 68
  • Cat 9

Top reported reactions (VEDDRA terms, top entries)

  • Vomiting 33
  • Death by euthanasia 29
  • Other abnormal test result NOS 29
  • Death 25
  • Lethargy (see also Central nervous system depression in 'Neurological') 25
  • Hypotension 24
  • Anorexia 22
  • Anaemia NOS 18
  • Elevated alanine aminotransferase (ALT) 18
  • Hypoalbuminaemia 17

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b21.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).