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FDA ADE reports for Moraxella Bovis Bacterin

ade_moraxella_bovis_bacterin_adverse_events

ade en 2026-07-22

Moraxella Bovis 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. Moraxella Bovis Bacterin is a active ingredient.

Total reports

Moraxella Bovis Bacterin: 22

Reports by species (top entries)

  • Cattle 22

Top reported reactions (VEDDRA terms, top entries)

  • Lack of efficacy - NOS 8
  • Death 4
  • Nasal discharge 2
  • Partial lack of efficacy 2
  • Pink eye 2
  • Pneumonia 2
  • Rectal prolapse 2
  • Sudden death 2
  • Abortion 1
  • Acute (interstitial) pneumonia/pleuropneumonia 1

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b26.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).