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FDA ADE reports for Moxidectin — total reports, species & reaction breakdown

ade_moxidectin_adverse_events

ade 200 tok en 2026-07-21

Moxidectin — 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. Moxidectin is a veterinary active ingredient.

Total reports

Moxidectin: 96700

Reports by species (top entries)

  • Dog 73342
  • Cat 11233
  • Horse 1735
  • Cattle 1314
  • Human 1013
  • Goat 96

Top reported reactions (VEDDRA terms, top entries)

  • Vomiting 15176
  • Lack of efficacy (endoparasite) - heartworm 10774
  • Lethargy (see also Central nervous system depression in 'Neurological') 6520
  • Diarrhoea 6165
  • Lack of efficacy (endoparasite) - hookworm 5586
  • Anaphylaxis 5115
  • Pruritus 4153
  • Facial swelling (see also 'Skin') 3736
  • Anorexia 3729
  • Lack of efficacy (ectoparasite) - flea 3463

"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