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FDA ADE reports for Febantel (prodrug anthelmintic (tapeworm / hookworm, dogs & cats)) — total reports, species & reaction breakdown

ade_febantel_adverse_events

ade en 2026-07-22

Febantel — 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. Febantel is a prodrug anthelmintic (tapeworm / hookworm, dogs & cats).

Total reports

Febantel: 5831

Reports by species (top entries)

  • Dog 5463
  • Cat 42
  • Cockatiel 4
  • Human 4
  • Horse 2
  • Cattle 1

Top reported reactions (VEDDRA terms, top entries)

  • Vomiting 2057
  • Emesis 647
  • Emesis (multiple) 623
  • Diarrhoea 563
  • Lethargy (see also Central nervous system depression in 'Neurological') 426
  • Lack of efficacy (endoparasite) - tapeworm 367
  • Lack of efficacy (endoparasite) - hookworm 296
  • Overdose 248
  • Hyperactivity 235
  • Anorexia 233

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

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b8.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

  • openFDA animalandveterinary/event.json (FDA CVM ADE), pulled 2026-07-22