โ† All Topics / ade

FDA ADE reports for Ceftiofur

ade_ceftiofur_crystalline_free_acid_adverse_events

ade en 2026-07-22

Ceftiofur โ€” 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. Ceftiofur is a active ingredient.

Total reports

Ceftiofur: 2132

Reports by species (top entries)

  • Cattle 967
  • Horse 882
  • Human 77
  • Pig 33
  • Cat 14
  • Donkey 12

Top reported reactions (VEDDRA terms, top entries)

  • Death 567
  • Injection site swelling 475
  • Lack of efficacy (bacteria) - NOS 330
  • Lack of efficacy - NOS 287
  • Injection site pain 235
  • Fever 164
  • Death by euthanasia 109
  • CULTURE/TITER DATA ABNORMAL 90
  • Colic 88
  • Injection site inflammation 84

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b10.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).