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FDA ADE reports for Leptospira Canicola Bacterin

ade_leptospira_canicola_bacterin_adverse_events

ade en 2026-07-22

Leptospira Canicola Bacterin 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. Leptospira Canicola Bacterin is a active ingredient.

Total reports

Leptospira Canicola Bacterin: 53

Reports by species (top entries)

  • Cattle 52
  • Goat 1

Top reported reactions (VEDDRA terms, top entries)

  • Death 24
  • Lack of efficacy - NOS 22
  • Necropsy performed 7
  • Lack of efficacy (bacteria) - NOS 4
  • Death by euthanasia 3
  • Lack of efficacy (virus) - NOS 3
  • Lack of efficacy (virus) - bovine viral diarrhoea virus 3
  • Abortion 2
  • CULTURE/TITER DATA ABNORMAL 2
  • Injection site lump 2

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b24.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).