FDA ADE reports for Frunevetmab (anti-NGF monoclonal antibody (feline osteoarthritis pain)) — total reports, species & reaction breakdown

ade_frunevetmab_adverse_events

ade en 2026-07-22

Frunevetmab — 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. Frunevetmab is a anti-NGF monoclonal antibody (feline osteoarthritis pain).

Total reports

Frunevetmab: 7813

Reports by species (top entries)

Cat 7616
Human 81
Dog 6
Cougar 1
Lynx 1
Other 1

Top reported reactions (VEDDRA terms, top entries)

Skin scab 837
Vomiting 799
Lethargy (see also Central nervous system depression in Neurological) 695
Lack of efficacy - NOS 643
Pruritus 637
Weight loss 499
Death by euthanasia 498
Diarrhoea 444
Not eating 428
Skin lesion NOS 369

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

Source JSON: pdf-raw/ade/ade_active_ingredients_2026-07-22_b8.json (openFDA animalandveterinary/event.json, pulled 2026-07-22).

Sources

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

Machine access

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