FDA ADE reports for Campylobacter Fetus Bacterin

ade_campylobacter_fetus_bacterin_adverse_events

ade en 2026-07-22

Campylobacter Fetus Bacterin — 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).

Sources

FDA ADE reports for Campylobacter Fetus Bacterin (active ingredient) — total reports, species & reaction breakdown

Source document: FDA FAERS / openFDA Animal & Veterinary Event Reports

US FDA Center for Veterinary Medicine (openFDA animal & veterinary event database)retrieved 2026-07-22

Verification file: pdf-raw/ade/ade_active_ingredients_2026-07-22_b29.json

Link points to the issuing authority's site; a direct document link is still being verified.

Machine access

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