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FDA ADE reports for ivermectin (macrocyclic lactone (endectocide: heartworm/parasite)) — total reports, species & reaction breakdown

ade_ivermectin_adverse_events

ade 205 tok en 2026-07-21

ivermectin — 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 2026-07-21. Counts are report-level: one report may list multiple reactions and multiple animals, so figures are not additive and do not imply causation. ivermectin is a macrocyclic lactone (endectocide: heartworm/parasite).

Total reports

ivermectin: 194447

Reports by species (top entries)

  • Dog 167897
  • Horse 3499
  • Cattle 2458
  • Cat 1093
  • Human 739
  • Sheep 250

Top reported reactions (VEDDRA terms, top entries)

  • INEFFECTIVE, HEARTWORM LARVAE 37191
  • Lack of efficacy (endoparasite) - hookworm 26113
  • Lack of efficacy (endoparasite) - heartworm 24396
  • Vomiting 23145
  • Digestive tract disorder NOS 16792
  • INEFFECTIVE, ASCARIDS NOS 11897
  • Diarrhoea 10122
  • Cardiac disorder NOS 10105
  • Lack of efficacy - NOS 8927
  • Tablets, Abnormal 8038

"Lack of efficacy" terms denote product-performance reports, not adverse reactions.

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-21.json (openFDA animalandveterinary/event.json, pulled 2026-07-21).

Sources

  • openFDA animalandveterinary/event.json (FDA CVM adverse event reports), pulled 2026-07-21