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

ade_pyrantel_adverse_events

ade 200 tok en 2026-07-21

Pyrantel — 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. Pyrantel is a veterinary active ingredient.

Total reports

Pyrantel: 251645

Reports by species (top entries)

  • Dog 229742
  • Cat 1996
  • Horse 946
  • Human 244
  • Other 40
  • Other Canids 10

Top reported reactions (VEDDRA terms, top entries)

  • Vomiting 37796
  • INEFFECTIVE, HEARTWORM LARVAE 35856
  • Lack of efficacy (endoparasite) - hookworm 31833
  • Lack of efficacy (endoparasite) - heartworm 28958
  • Digestive tract disorder NOS 16840
  • Diarrhoea 16144
  • INEFFECTIVE, ASCARIDS NOS 12018
  • Cardiac disorder NOS 10073
  • Lethargy (see also Central nervous system depression in 'Neurological') 9657
  • Lack of efficacy (endoparasite) - roundworm NOS 9213

"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