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)
active substance
Flunixin Meglumine — veterinary medicines
Authorised animal medicines containing Flunixin Meglumine 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
39 authorised products across national registers.
United States — DailyMed (NLM)
- BANAMINE · 3 pack sizes
- FLU-NIX
- FLUNAZINE · 2 pack sizes
- FLUNAZINE-S
- FLUNINE
- FLUNIXIN · 4 pack sizes
- FLUNIXIN-S
- PREVAIL · 2 pack sizes
- VETAMEG · 4 pack sizes
- VETAMEG S
United States — FDA Green Book
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 Flunixin Meglumine, by species — reported counts, not proven reactions.
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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