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FDA ADE reports for Tiletamine

ade_tiletamine_adverse_events

ade en 2026-07-22

Tiletamine 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. Tiletamine is a active ingredient.

Total reports

Tiletamine: 234

Reports by species (top entries)

  • Dog 116
  • Cat 81
  • White tailed deer 2
  • Buffalo 1
  • Human 1

Top reported reactions (VEDDRA terms, top entries)

  • Lack of efficacy - NOS 79
  • Death 24
  • Vomiting 15
  • Seizure NOS 10
  • Appearance, Abnormal 9
  • Vocalisation 9
  • Anorexia 8
  • Ataxia 8
  • Recovery prolonged 8
  • Respiratory arrest 8

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b17.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).