Tilmicosin — 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. Tilmicosin is a active ingredient.
Total reports
Tilmicosin: 3572
Reports by species (top entries)
- Human 2275
- Cattle 825
- Pig 150
- Sheep 118
- Goat 62
- Dog 12
Top reported reactions (VEDDRA terms, top entries)
- Accidental exposure 2203
- Unclassifiable adverse event 2095
- Death 717
- No sign 659
- Injection site pain 276
- Injection site swelling 242
- Sensory abnormality NOS 232
- Lack of efficacy (bacteria) - NOS 231
- Injection site bleeding 217
- Nausea 146
Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b9.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).