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FDA ADE reports for Erythromycin

ade_erythromycin_adverse_events

ade en 2026-07-22

Erythromycin — 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. Erythromycin is a active ingredient.

Total reports

Erythromycin: 87

Reports by species (top entries)

  • Cat 36
  • Dog 18
  • Cattle 14
  • Human 4
  • Horse 1
  • Pig 1

Top reported reactions (VEDDRA terms, top entries)

  • Death 9
  • Death by euthanasia 7
  • Lack of efficacy - NOS 7
  • Other abnormal test result NOS 7
  • Vomiting 7
  • Digestive tract disorder NOS 6
  • Hypersalivation 6
  • Neutrophilia 6
  • Ocular discharge 6
  • Product syringe issue 6

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b21.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

FDA ADE reports for Erythromycin (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_b21.json

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