Lokivetmab — 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. Lokivetmab is a active ingredient.
Total reports
Lokivetmab: 199
Reports by species (top entries)
- Dog 199
Top reported reactions (VEDDRA terms, top entries)
- Lack of efficacy - NOS 29
- Vomiting 21
- Lethargy (see also Central nervous system depression in Neurological) 18
- Decreased appetite 17
- Diarrhoea 13
- Elevated serum alkaline phosphatase (SAP) 13
- Elevated alanine aminotransferase (ALT) 12
- Lethargy (see also Central nervous system depression in 'Neurological') 11
- Abnormal adrenocorticotropic hormone (ACTH) stimulation test 10
- Ear discharge 10
Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b18.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).