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FDA ADE reports for Campylobacter Fetus Bacterin

ade_campylobacter_fetus_bacterin_adverse_events

ade en 2026-07-22

Campylobacter Fetus 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. Campylobacter Fetus Bacterin is a active ingredient.

Total reports

Campylobacter Fetus Bacterin: 9

Reports by species (top entries)

  • Cattle 9

Top reported reactions (VEDDRA terms, top entries)

  • Lack of efficacy - NOS 4
  • Death 2
  • Lack of efficacy (endoparasite) - Trichostrongylus 2
  • Injection site granuloma 1
  • Laceration 1
  • Lack of efficacy (bacteria) - NOS 1
  • Lack of efficacy (endoparasite) - Cooperia 1
  • Lack of efficacy (endoparasite) - Ostertagia/Teladorsagia 1
  • Lack of efficacy (endoparasite) - roundworm NOS 1
  • Lack of efficacy (endoparasite) - tapeworm 1

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b29.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).