Category: B
Betafuse for dogs is used in the treatment of acute surface pyoderma in the dog, such as acute moist dermatitis (‘hot spots’) and intertrigo (skin fold dermatitis), caused by Gram-positive bacteria sensitive to fusidic acid.
This medication comes in an off-white to white gel and the active ingredients are Betamethasone Valerate and Fusidic Acid. Shelf life after first opening the container is 8 weeks.
Betafuse 1 mg/g + 5 mg/g Gel is a prescription-only medication. This means that before you complete your purchase, you are required to upload a prescription through our online portal.
Once our team has confirmed you've ordered the right medication for your dogs, we will send out your order. It's a simple process that means you can buy Betafuse online instead of going to your vet every month.
To apply Betafuse gel the hairs covering the lesions should first be gently clipped. The affected area should then be thoroughly cleaned with an antiseptic wash before daily application of Betafuse gel.
The amount applied should cover the affected area in a thin layer. Apply approximately 0.5 cm length of gel per 8 cm2 of lesion, twice daily, for a minimum period of 5 days. Treatment should continue for 48 hours after the lesion has resolved. The treatment period should not exceed 7 days.
Official, national and regional antimicrobial policies should be taken into account when the product is used.
It is recommended that use of the product should be based on bacteriological sampling and susceptibility testing. If this is not possible, therapy should be based on epidemiological information about susceptibility of the target bacteria. Use of the product deviating from the instructions given in the SPC may increase the prevalence of bacteria resistant to fusidic acid.
Use of the product in association with occlusive bandages or dressings should be avoided.
Betamethasone valerate can be absorbed percutaneously and may cause temporary suppression of adrenal function.
In dogs with treated or stabilised Cushing’s syndrome, only use the product after careful consideration of the benefit risk balance by the responsible veterinary surgeon.
Avoid eye contact.
The dog should be prevented from licking treated lesions and so ingesting the product.
Where there is a risk of self-trauma or a risk of accidental transfer to the eye, for example, application of the product on the forelimb, preventative measures such as the use of a protective collar should be considered.
Special precautions to be taken by the person administering the veterinary medicinal product to animals
People with known hypersensitivity to the active ingredients or to any of the excipients should avoid contact with the veterinary medicinal product.
Corticosteroids may produce irreversible effects in the skin; they can be absorbed and may have harmful effects, especially with frequent and extensive contact or in pregnancy. Pregnant women should take special care to avoid accidental exposure.
Always wear single-use impermeable gloves when applying this product to animals.
Wash hands after having applied the product.
Care should be taken to avoid contact with treated areas of the animal, for the duration of the treatment period.
Care should be taken to avoid accidental ingestion by a child. In the case of accidental ingestion, seek medical advice immediately and show the package leaflet to the physician.
Target species
Dog.
Indications for use, specifying the target species
For the treatment of acute surface pyoderma in the dog, such as acute moist dermatitis (‘hot spots’) and intertrigo (skin fold dermatitis), caused by Gram-positive bacteria sensitive to fusidic acid.
Contraindications
See section "Use during pregnancy, lactation or lay".
Special warnings for each target species
Pyoderma is often secondary in nature. The underlying cause should be identified and treated.
Special precautions for use
Special precautions for use in animals
Official, national and regional antimicrobial policies should be taken into account when the product is used.
It is recommended that use of the product should be based on bacteriological sampling and susceptibility testing. If this is not possible, therapy should be based on epidemiological information about susceptibility of the target bacteria. Use of the product deviating from the instructions given in the SPC may increase the prevalence of bacteria resistant to fusidic acid.
Use of the product in association with occlusive bandages or dressings should be avoided.
Betamethasone valerate can be absorbed percutaneously and may cause temporary suppression of adrenal function.
In dogs with treated or stabilised Cushing’s syndrome, only use the product after careful consideration of the benefit risk balance by the responsible veterinary surgeon.
Avoid eye contact.
The dog should be prevented from licking treated lesions and so ingesting the product.
Where there is a risk of self-trauma or a risk of accidental transfer to the eye, for example, application of the product on the forelimb, preventative measures such as the use of a protective collar should be considered.
Special precautions to be taken by the person administering the veterinary medicinal product to animals
People with known hypersensitivity to the active ingredients or to any of the excipients should avoid contact with the veterinary medicinal product.
Corticosteroids may produce irreversible effects in the skin; they can be absorbed and may have harmful effects, especially with frequent and extensive contact or in pregnancy. Pregnant women should take special care to avoid accidental exposure.
Always wear single-use impermeable gloves when applying this product to animals.
Wash hands after having applied the product.
Care should be taken to avoid contact with treated areas of the animal, for the duration of the treatment period.
Care should be taken to avoid accidental ingestion by a child. In the case of accidental ingestion, seek medical advice immediately and show the package leaflet to the physician.
Adverse reactions (frequency and seriousness)
Prolonged and intensive use of topical corticosteroid preparations or treatment of a large cutaneous surface (>10%) is known to trigger local or systemic effects including suppression of adrenal function, thinning of the epidermis and delayed healing.
Locally applied steroids may cause depigmentation of the skin.
Discontinue use if hypersensitivity develops to the product.
Use during pregnancy, lactation or lay
The use of the product during pregnancy and lactation is not recommended. The safety of the product has not been assessed during pregnancy and lactation.
Laboratory studies have demonstrated that topical application of betamethasone in pregnant females may lead to malformations in neonates. Small amounts of betamethasone can pass the blood-milk-barrier.
Interaction with other medicinal products and other forms of interaction
Concurrent treatment with steroids and NSAIDs may increase the risk for the development of gastrointestinal ulcers.
Royal Mail 2nd Class / Parcel Force 48
UK to UK :Normally arrives in 2-4 business days.
UK to Ireland :Normally arrives in 4-6 business days
UK to EU Countries : Normally arrives in 6-10 working days depending on where the parcel is going
Please note standered delivery is none trackable , none insured , no responsabily for lose or Damage
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Royal Mail First Class / Parcel Force 24
UK to UK :Normally arrives in 1-2 business days.
UK to Ireland 3-4 business days
UK to EU Countries : Normally arrives in 6-10 working days depending on where the parcel is going
Please note :Trackable , Royal Mail insured up to £50.
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Parcel Force Express AM Guaranteed before Midday.
UK to UK only . UP to 5KG Max Weight
Arrives next day before 12 noon, requires a signature.
Parcel Forcel Terms & Conditions apply
Important: Parcel Force advise that there are some postcodes where an extended delivery time exists, and may affect the date of delivery or the service is not available.
Category | POM-V |
Temperature | Ambient |
MA/VM/EU No: | 02000/4404 |
Species |
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VMD Link | Product Information Database (defra.gov.uk) |
NOAH Link | https://www.noahcompendium.co.uk/?id=-470335 |
Dosage | Amounts to be administered and administration route Cutaneous use. First, the hairs covering the lesions should be gently clipped. The affected area should then be thoroughly cleaned with an antiseptic wash before daily application of the gel. The amount applied should cover the affected area in a thin layer. Apply approximately 0.5 cm length of gel per 8 cm2 of lesion, twice daily, for a minimum period of 5 days. Treatment should continue for 48 hours after the lesion has resolved. The treatment period should not exceed 7 days. If there is no response within three days, or the condition deteriorates, the diagnosis should be re-evaluated. Overdose (symptoms, emergency procedures, antidotes), if necessary For possible signs see "Adverse reactions (frequency and seriousness)" above. |
Withdrawals |