Species: Bovine
0.3 μg/kg
European Union
Species: Bovine · Tissue: Milk
Marker residue: Betamethasone
Therapeutic class: Corticoides/Glucocorticoides
active substance
Betamethasone — veterinary medicines
Authorised animal medicines containing Betamethasone 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
DogsDog or cat
Authorised products
20 authorised products across national registers.
United Kingdom — VMD
- Betafuse 1 mg/g + 5 mg/g Gel for Dogs · 2 pack sizes
- Fudacort 5 mg/g +1 mg/g Gel for Dogs
- Fuselieve 1 mg/g + 5 mg/g Gel for Dogs · 2 pack sizes
- Isaderm 5 mg/g + 1 mg/g Gel for Dogs · 2 pack sizes
- Otomax Ear Drops Suspension · 2 pack sizes
- Trigoderm Gel 0.5% w/w Fusidic Acid, 0.1% w/w Betamethasone
Canada — Health Canada DPD
Australia — APVMA PUBCRIS
Residue limits (MRL)
Species: Bovine, porcine
0.75 μg/kg
European Union
Species: Bovine, porcine · Tissue: Kidney
Marker residue: Betamethasone
Therapeutic class: Corticoides/Glucocorticoides
Species: Bovine, porcine
2 μg/kg
European Union
Species: Bovine, porcine · Tissue: Liver
Marker residue: Betamethasone
Therapeutic class: Corticoides/Glucocorticoides
Species: Bovine, porcine
0.75 μg/kg
European Union
Species: Bovine, porcine · Tissue: Muscle
Marker residue: Betamethasone
Therapeutic class: Corticoides/Glucocorticoides
Antimicrobial resistance surveillance
No antimicrobial-resistance surveillance is recorded for this substance.
Reported adverse events (openFDA)
Spontaneous adverse-event reports that name Betamethasone, by species — reported counts, not proven reactions.
Dog
2,037 reported events
openFDA
Top reactions: Deafness (1,427) · Lack of efficacy - NOS (1,260) · Vomiting (254) · Partial deafness (246) · Ear discharge (187)
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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