Darbepoetin — 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. Darbepoetin is a active ingredient.
Total reports
Darbepoetin: 20
Reports by species (top entries)
- Cat 20
Top reported reactions (VEDDRA terms, top entries)
- Lack of efficacy - NOS 7
- Vomiting 4
- Elevated blood urea nitrogen (BUN) 2
- Elevated creatinine 2
- Elevated symmetrical dimethylarginine (SDMA) 2
- Lethargy (see also Central nervous system depression in Neurological) 2
- Agitation 1
- Anaemia NOS 1
- Application site skin scaling 1
- Ataxia 1
Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b27.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).