Indications
Psoriasis of the scalp.
Mild to moderate psoriasis of other parts of the body.
$192.00
Active ingredient: | |
---|---|
Dosage form: |
Psoriasis of the scalp.
Mild to moderate psoriasis of other parts of the body.
of 1 g of gel contains:
Active ingredients:
Betamethasone dipropionate 0.643 mg (equivalent to betamethasone 0.5 mg)
calcipotriol monohydrate 0.052 mg (equivalent to calcipotriol 0.05 mg).
Auxiliary substances:
liquid paraffin (contains about 10 ppm alpha-tocopherol) 820 mg,
polypropylene glycol stearate (PPG – 15) (contains 0.1% butylhydroxytoluene) 160 mg,
hydrogenated castor oil 20 mg.
>
of 1 g of gel contains:
Active ingredients:
betamethasone dipropionate 0.643 mg (equivalent to betamethasone 0.5 mg)
calcipotriol monohydrate 0.052 mg (equivalent to calcipotriol 0.05 mg).
Auxiliary substances:
liquid paraffin (contains about 10 ppm alpha-tocopherol) 820 mg,
polypropylene glycol stearate (PPG – 15) (contains 0.1% butylhydroxytoluene) 160 mg,
hydrogenated castor oil 20 mg.
Psoriasis of the scalp.
Mild to moderate psoriasis of other parts of the body.
Side effects are classified according to the frequency of occurrence:
Eye disorders: infrequent – eye irritation.
From the skin and appendages of the skin: frequent-itching; infrequent-rash, burning sensation, pain, irritation, dermatitis, psoriasis exacerbation, folliculitis, dry skin, acne, pustular psoriasis. Calcipotriol can cause local skin irritation, itching, burning and tingling, dry skin, erythema, rash, dermatitis, eczema, psoriasis exacerbation, hyper – and photosensitivity reactions, including very rare cases of angioedema and facial edema. Long-term external use of betamethasone (dipropionate) is associated with the development of skin atrophy, telangiectasia, striae, folliculitis, hypertrichosis, perioral dermatitis, allergic contact dermatitis, depigmentation, colloidal skin degeneration, as well as an increased risk of generalized pustular psoriasis.
Systemic reactions: calcipotriol-related (very rare) – hypercalcemia or hypercalciuria; betamethasone-related (rare, but sometimes severe, especially with prolonged use, on large surfaces and when using occlusive dressings) – suppression of the adrenal cortex, cataracts, infections, increased intraocular pressure. Systemic reactions occur more frequently when the drug is applied under occlusive dressings and when applied to thin skin and skin folds, as well as during long-term treatment when applied to large areas of the skin.
Externally.
Use in adults
Before using the drug, the bottle must be shaken. The gel is applied in a thin layer on the affected areas of the scalp or on psoriatic plaques of other parts of the body 1 time a day.
The maximum daily dose should not exceed 15 g; the maximum weekly dose should not exceed 100 g. The recommended duration of treatment is 4 weeks for psoriasis of the scalp and 8 weeks for skin lesions of other parts of the body. The area of application of the drug should not exceed 30% of the body surface.
The drug should remain on the skin during the night or day to achieve optimal therapeutic effect. Repeated use of Xamiol® is possible under medical supervision.
Symptoms: increased blood calcium content, rapidly restored upon discontinuation of the drug; suppression of the pituitary-adrenal system with the development of reversible secondary adrenal insufficiency.
Treatment: discontinue the drug and perform symptomatic therapy. In cases of chronic toxicity, corticosteroids should be discontinued gradually.
Gel for external use
Do not use the product on the mucous membranes.
Use the product with caution when applied to the face and genitals.
In case of accidental contact with the eyes, undesirable side effects may occur in the form of eye and facial skin irritation, conjunctivitis. In case of accidental contact with the eyes, they should be rinsed with running water.
After applying the drug, you should wash your hands.
If secondary infections develop, antimicrobial therapy should be prescribed. Discontinuation of psoriasis treatment with topical corticosteroids may be associated with a risk of developing generalized pustular psoriasis and a withdrawal effect. Therefore, after discontinuation of such treatment, it is necessary to continue clinical monitoring of the patient.
During treatment with XAMIOL®, the patient is advised to limit or avoid excessive exposure to natural or artificial sunlight. Calcipotriol (and preparations containing it) is allowed to be used topically in combination with ultraviolet radiation only in cases where the attending physician considers the risk of undesirable side effects associated with such treatment to be justified.
XAMIOL contains butylhydroxytoluene (E 321), which may cause local skin reactions (e. g. contact dermatitis) or irritation of the eyes and mucous membranes.
To achieve an optimal therapeutic effect, it is not recommended to take a shower/bath or wash your hair (in the case of treatment of scalp lesions) immediately after using the drug.
Store at a temperature not exceeding 25 °C. Do not store in the refrigerator. Store in a cardboard box to protect from light. Keep out of reach of children.
life is 2 years.
Betamethasone, Calcipotriol
gel for external use
Reviews
There are no reviews yet