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FDA ADE reports for Laidlomycin Propionate Potassium

ade_laidlomycin_propionate_adverse_events

ade en 2026-07-22

Laidlomycin Propionate Potassium — 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. Laidlomycin Propionate Potassium is a active ingredient.

Total reports

Laidlomycin Propionate Potassium: 10

Reports by species (top entries)

  • Cattle 7

Top reported reactions (VEDDRA terms, top entries)

  • Death 2
  • Lack of efficacy (protozoa) - Coccidia 2
  • Ruminal bloat 2
  • Unrelated death 2
  • Abnormal necropsy finding 1
  • Blood in faeces 1
  • Color, Abnormal 1
  • Cough 1
  • Hard, clumping 1
  • INEFFECTIVE, WEIGHT INC 1

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b30.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

FDA ADE reports for Laidlomycin Propionate Potassium (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_b30.json

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