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active substance

Butorphanol Tartrate — veterinary medicines

Authorised animal medicines containing Butorphanol Tartrate 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.

Authorised products

12 authorised products across national registers.

Australia — APVMA PUBCRIS

United States — DailyMed (NLM)

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 Butorphanol Tartrate, by species — reported counts, not proven reactions.

Cat

849 reported events

openFDA

Top reactions: Death (187) · Cardiac arrest (94) · Fever (68) · Anorexia (66) · Ataxia (64)

Horse

172 reported events

openFDA

Top reactions: INEFFECTIVE, SEDATION (30) · Death (27) · Ataxia (19) · Underdose (18) · Death by euthanasia (12)

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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