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FDA ADE reports for Molidustat

ade_molidustat_adverse_events

ade en 2026-07-22

Molidustat 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. Molidustat is a active ingredient.

Total reports

Molidustat: 383

Reports by species (top entries)

  • Cat 339
  • Dog 1

Top reported reactions (VEDDRA terms, top entries)

  • Lack of efficacy - NOS 105
  • Vomiting 49
  • Weight loss 39
  • Decreased haematocrit 37
  • Death by euthanasia 35
  • Elevated creatinine 34
  • Lethargy (see also Central nervous system depression in Neurological) 31
  • Pica NOS 31
  • Not eating 29
  • Elevated blood urea nitrogen (BUN) 28

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b15.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).