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United States — FDA Green Book

Banamine® , Banamine®-S

Authorised animal medicine, recorded in United States — FDA Green Book. This is a neutral reference record 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.

Active substances

Authorisation

No. 101-479

Source

United States — FDA Green Book. Original source.

Other Flunixin Meglumine medicines

Reported adverse events (openFDA)

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

Horse

492 reported events

openFDA

Top reactions: Injection site swelling (111) · Death (96) · Fever (72) · Death by euthanasia (53) · Collapse (see also 'Cardio-vascular' and 'Systemic disorders') (51)

Cattle

189 reported events

openFDA

Top reactions: Death (177) · Lack of efficacy - NOS (44) · Collapse (see also 'Cardio-vascular' and 'Systemic disorders') (26) · Anaphylaxis (24) · Lack of efficacy (bacteria) - NOS (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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