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FDA ADE reports for Lubabegron

ade_lubabegron_adverse_events

ade en 2026-07-22

Lubabegron 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. Lubabegron is a active ingredient.

Total reports

Lubabegron: 40

Reports by species (top entries)

  • Cattle 37

Top reported reactions (VEDDRA terms, top entries)

  • Death 22
  • Unclassifiable adverse event 18
  • Lameness 12
  • Bloated 10
  • Found dead 9
  • Pneumonia 9
  • Respiratory tract disorder NOS 6
  • Peritonitis 5
  • Ruminal bloat 5
  • Behavioural disorder NOS 4

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b25.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).