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active substance

Meloxicam — veterinary medicines

Authorised animal medicines containing Meloxicam 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

ChevalBovinsPorcinsPerrosBovinoCaballosPorcinoGatosCobayasTernerosBovino rumianteTerneros prerrumiantesCatsDogsCattleSwine (pigs)SheepPigsHorsesGuinea Pig

Authorised products

774 authorised products across national registers.

Spain — CIMAVet (AEMPS)

United States — DailyMed (NLM)

Italy — Ministero della Salute

Australia — APVMA PUBCRIS

France — ANSES-ANMV

United Kingdom — VMD

Residue limits (MRL)

No residue limits (MRL) are recorded for this substance.

Antimicrobial resistance surveillance

No antimicrobial-resistance surveillance is recorded for this substance.

Reported adverse events (openFDA)

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

Dog

7,913 reported events

openFDA

Top reactions: Vomiting (2,071) · Anorexia (1,257) · Diarrhoea (1,041) · Depression (768) · Elevated blood urea nitrogen (BUN) (688)

Cat

3,587 reported events

openFDA

Top reactions: Anorexia (1,300) · Elevated creatinine (1,253) · Elevated blood urea nitrogen (BUN) (1,219) · Vomiting (1,006) · Depression (896)

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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