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FDA ADE reports for Mycoplasma Bovis

ade_mycoplasma_bovis_adverse_events

ade en 2026-07-22

Mycoplasma Bovis — 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. Mycoplasma Bovis is a active ingredient.

Total reports

Mycoplasma Bovis: 15

Reports by species (top entries)

  • Cattle 15

Top reported reactions (VEDDRA terms, top entries)

  • Death 12
  • Lack of efficacy - NOS 8
  • Lack of efficacy (mycoplasma) - NOS 3
  • Lack of efficacy (virus) - coronavirus - NOS 3
  • Necropsy performed 3
  • Lack of efficacy (bacteria) - Histophilus somni 2
  • Lack of efficacy (bacteria) - Mannheimia haemolytica 2
  • Lack of efficacy (bacteria) - Pasteurella multocida 2
  • Lack of efficacy (virus) - bovine viral diarrhoea virus 2
  • Appetite loss 1

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b28.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

FDA ADE reports for Mycoplasma Bovis (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_b28.json

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