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FDA ADE reports for Avermectin

ade_avermectin_adverse_events

ade en 2026-07-22

Avermectin 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. Avermectin is a active ingredient.

Total reports

Avermectin: 2

Reports by species (top entries)

  • Cattle 2

Top reported reactions (VEDDRA terms, top entries)

  • Lack of efficacy (bacteria) - NOS 2
  • Death 1
  • Drug dose administration interval too short 1
  • Overdose 1
  • PR-LUNG(S), LESION(S) 1

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b34.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).