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FDA ADE reports for Telmisartan — total reports, species & reaction breakdown

ade_telmisartan_adverse_events

ade 200 tok en 2026-07-22

Telmisartan — 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. Telmisartan is a veterinary active ingredient.

Total reports

Telmisartan: 694

Reports by species (top entries)

  • Cat 420
  • Dog 198
  • Human 2

Top reported reactions (VEDDRA terms, top entries)

  • Vomiting 133
  • Lack of efficacy - NOS 118
  • Weight loss 60
  • Diarrhoea 58
  • Elevated creatinine 50
  • Decreased appetite 49
  • Death by euthanasia 42
  • Lethargy (see also Central nervous system depression in Neurological) 37
  • Elevated blood urea nitrogen (BUN) 34
  • Lethargy (see also Central nervous system depression in 'Neurological') 33

"Lack of efficacy" terms denote product-performance reports, not adverse reactions.

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b6.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

  • openFDA animalandveterinary/event.json (FDA CVM adverse event reports), pulled 2026-07-22