Rabacfosadine Succinate — 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. Rabacfosadine Succinate is a active ingredient.
Total reports
Rabacfosadine Succinate: 341
Reports by species (top entries)
- Dog 338
- Cat 1
- Human 1
- Other Mammals 1
Top reported reactions (VEDDRA terms, top entries)
- Anorexia 109
- Diarrhoea 99
- Lethargy (see also Central nervous system depression in 'Neurological') 88
- Death by euthanasia 75
- Weight loss 75
- Lack of efficacy - NOS 68
- Elevated liver enzymes 46
- Neutropenia 45
- Alopecia 40
- Vomiting 40
Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b16.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).