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FDA ADE reports for Tigilanol Tiglate

ade_tigilanol_tiglate_adverse_events

ade en 2026-07-22

Tigilanol Tiglate 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. Tigilanol Tiglate is a active ingredient.

Total reports

Tigilanol Tiglate: 1998

Reports by species (top entries)

  • Dog 1974
  • Human 9
  • Horse 5
  • Cat 2
  • Other 1

Top reported reactions (VEDDRA terms, top entries)

  • Lack of efficacy - NOS 853
  • Injection site swelling 688
  • Wound 400
  • Injection site pain 298
  • Pain NOS 290
  • Swelling NOS 285
  • Injection site necrosis 233
  • Swollen limb 223
  • Injection site complication NOS 214
  • Injection site bruising 206

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b10.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).