โ† All Topics / ade

FDA ADE reports for Moraxella Bovis Bacterin Toxoid

ade_moraxella_bovis_bacterin_toxoid_adverse_events

ade en 2026-07-22

Moraxella Bovis Bacterin Toxoid 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 Toxoid is a active ingredient.

Total reports

Moraxella Bovis Bacterin Toxoid: 28

Reports by species (top entries)

  • Cattle 28

Top reported reactions (VEDDRA terms, top entries)

  • Death 12
  • Lack of efficacy - NOS 11
  • Lack of efficacy (bacteria) - NOS 7
  • CULTURE/TITER DATA ABNORMAL 3
  • Necropsy performed 3
  • PR-LIVER, LESION(S) 2
  • Abnormal necropsy finding 1
  • Acute (interstitial) pneumonia/pleuropneumonia 1
  • Anorexia 1
  • Blindness 1

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