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active substance

Firocoxib — veterinary medicines

Authorised animal medicines containing Firocoxib across national registers. Regulatory residue limits (MRL) and antimicrobial-resistance surveillance are shown when on record. This is a neutral reference and does not provide dosing or veterinary advice.
Reference information only — not veterinary advice and not a dosing source. Always consult a licensed veterinarian before giving any medicine to an animal.

Target species

ChevalPerrosCaballosDogsHorses

Authorised products

156 authorised products across national registers.

Italy — Ministero della Salute

United States — DailyMed (NLM)

Canada — Health Canada DPD

Residue limits (MRL)

Species: Equidae

15 μg/kg

European Union

Species: Equidae · Tissue: Fat

Marker residue: Firocoxib

Therapeutic class: Anti-inflammatory agents/Nonsteroidal anti-inflammatory agents

Species: Equidae

10 μg/kg

European Union

Species: Equidae · Tissue: Kidney

Marker residue: Firocoxib

Therapeutic class: Anti-inflammatory agents/Nonsteroidal anti-inflammatory agents

Species: Equidae

60 μg/kg

European Union

Species: Equidae · Tissue: Liver

Marker residue: Firocoxib

Therapeutic class: Anti-inflammatory agents/Nonsteroidal anti-inflammatory agents

Species: Equidae

10 μg/kg

European Union

Species: Equidae · Tissue: Muscle

Marker residue: Firocoxib

Therapeutic class: Anti-inflammatory agents/Nonsteroidal anti-inflammatory agents

Antimicrobial resistance surveillance

No antimicrobial-resistance surveillance is recorded for this substance.

Reported adverse events (openFDA)

Spontaneous adverse-event reports that name Firocoxib, by species — reported counts, not proven reactions.

Dog

6,630 reported events

openFDA

Top reactions: Vomiting (2,519) · Anorexia (1,326) · Elevated blood urea nitrogen (BUN) (1,078) · Diarrhoea (932) · Elevated creatinine (807)

Horse

402 reported events

openFDA

Top reactions: Diarrhoea (32) · Lack of efficacy - NOS (31) · Colic (26) · Anorexia (24) · Death by euthanasia (24)

Source: openFDA Animal & Veterinary adverse-event reports.

Surveillance reference only — these are spontaneous adverse-event report counts, not proven adverse reactions, not causation and not a measure of any product's risk or safety. Always consult a licensed veterinarian.

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