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

ade_levetiracetam_adverse_events

ade 200 tok en 2026-07-21

Levetiracetam — 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. Levetiracetam is a veterinary active ingredient.

Total reports

Levetiracetam: 686

Reports by species (top entries)

  • Dog 647
  • Cat 37
  • Human 1

Top reported reactions (VEDDRA terms, top entries)

  • Seizure NOS 323
  • Vomiting 74
  • Death by euthanasia 73
  • Lethargy (see also Central nervous system depression in 'Neurological') 58
  • Ataxia 55
  • Behavioural disorder NOS 37
  • Elevated alanine aminotransferase (ALT) 37
  • Tremor 37
  • Lack of efficacy - NOS 36
  • Diarrhoea 35

"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