โ† All Topics / ade

FDA ADE reports for Guaifenesin

ade_guaifenesin_adverse_events

ade en 2026-07-22

Guaifenesin 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. Guaifenesin is a active ingredient.

Total reports

Guaifenesin: 54

Reports by species (top entries)

  • Horse 20
  • Dog 19
  • Cattle 1
  • Human 1

Top reported reactions (VEDDRA terms, top entries)

  • Lack of efficacy - NOS 8
  • Death 7
  • Death by euthanasia 5
  • Diarrhoea 5
  • INEFFECTIVE, ANESTHESIA 5
  • Solution, Abnormal 5
  • Vomiting 5
  • Cardiac arrest 3
  • Dyspnoea 3
  • Hind limb ataxia 3

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b27.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).