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FDA ADE reports for Fusobacterium Necrophorum Bacterin

ade_fusobacterium_necrophorum_bacterin_adverse_events

ade en 2026-07-22

Fusobacterium Necrophorum 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. Fusobacterium Necrophorum Bacterin is a active ingredient.

Total reports

Fusobacterium Necrophorum Bacterin: 5

Reports by species (top entries)

  • Cattle 5

Top reported reactions (VEDDRA terms, top entries)

  • Death 4
  • Bloated 2
  • Lameness 2
  • Loss of condition 2
  • Pneumonia 2
  • Respiratory tract disorder NOS 2
  • Anaphylaxis 1
  • Collapse NOS (see also 'Cardio-vascular' and 'Neurological disorders') 1
  • Distress 1
  • General illness 1

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b31.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).