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Qui a deja utilis la creme daivobet

Therefore, during pregnancy, dovobet should only be used when the potential benefit justifies the potential risk. Breast-feeding Betamethasone passes into breast milk but risk of an adverse effect on the infant seems unlikely with therapeutic doses. There are no data on the excretion of calcipotriol in breast milk. Caution should be exercised when prescribing dovobet ointment to women who breast-feed. The patient should be instructed not to use dovobet on the breast when breast-feeding. Fertility Studies in rats with oral doses of calcipotriol or betamethasone dipropionate demonstrated no impairment of male and female fertility (see section.3). 4.7 Effects on ability to drive and use machines dovobet has no or negligible influence on the ability to drive and use machines.

dovobet creme

Unevaluated use, there is no experience with the use of dovobet in guttate psoriasis. Concurrent treatment and uv exposure, there is limited experience for dead the use of this medicinal product on the scalp. Dovobet ointment for body psoriasis lesions has been used in combination with dovobet gel for scalp psoriasis lesions, but there is limited experience of combination of dovobet with other topical anti-psoriatic products at the same treatment area, other anti-psoriatic medicinal products administered systemically or with. During dovobet treatment, physicians are recommended to advise patients to limit or avoid excessive exposure to either natural or artificial sunlight. Topical calcipotriol should be used with uvr only if the physician and patient consider that the potential benefits outweigh the potential risks (see section.3). Adverse reactions to excipients. Dovobet ointment contains butylhydroxytoluene (E321) as an excipient which may cause local skin reactions (e.g.

Contact dermatitis or irritation to the eyes and mucous membranes. 4.5 Interaction with other medicinal products and other forms of interaction no interaction studies have been performed with dovobet. 4.6 Pregnancy and lactation Pregnancy There are no adequate data from the use of dovobet in pregnant women. Studies in animals with glucocorticoids have shown reproductive toxicity (see section.3 but a number of epidemiological studies (less than 300 pregnancy outcomes) have not revealed congenital anomalies among infants born to women treated with corticosteroids during pregnancy. The potential risk for humans is uncertain.

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Dovobet contains a potent group iii-steroid and concurrent treatment with other steroids on the same treatment area must be avoided. Skin of the face and genitals are very sensitive to corticosteroids. The medicinal product should not be used in these areas. The patient must be instructed in correct use of the medicinal product to avoid application and accidental transfer to the face, mouth and eyes. Hands must be washed after each application to avoid accidental transfer to these areas.

Concomitant skin infections, when lesions become secondarily infected, they should be treated with antimicrobiological therapy. However, if infection worsens, treatment with corticosteroids should be stopped (see section.3). Discontinuation of treatment, when treating psoriasis with topical corticosteroids there may be a risk of generalised pustular psoriasis or of rebound effects when discontinuing treatment. Medical supervision should therefore continue in the post-treatment period. With long-term use there is an increased risk of local and systemic corticosteroid adverse reactions. The treatment should be discontinued in case of adverse reactions related to long-term use of corticosteroid (see section.8).

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Effects on endocrine system, dovobet ointment contains a potent group iii steroid and concurrent treatment with other steroids must be avoided. Adverse reactions found stockists in connection with systemic corticosteroid treatment, such as adrenocortical suppression or impact on the metabolic control of diabetes mellitus may occur also during topical corticosteroid treatment due to systemic absorption. Application under occlusive dressings should be avoided since it increases the systemic absorption of corticosteroids. Application on large areas of damaged skin or on mucous membranes or in skin folds should be avoided since it increases the systemic absorption of corticosteroids (see section a study in patients with both extensive scalp and extensive body psoriasis using a combination of high. Effects on calcium metabolism, due to the content of calcipotriol, hypercalcaemia may occur if the maximum daily dose (15 g) is exceeded. Serum calcium is normalised when treatment is discontinued. The risk of hypercalcaemia is minimal when the recommendations relevant to calcipotriol are followed. Treatment of more than 30 of the body surface should be avoided (see section.2).

dovobet creme

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Special populations, renal and hepatic impairment, the safety and efficacy of cream dovobet ointment in patients with severe renal insufficiency or severe hepatic disorders have not been evaluated. The safety and efficacy of dovobet ointment in children below 18 years have not been established. Currently available data in children aged 12 to 17 years are described in section.8 and.1 but no recommendation on a posology can be made. Method of administration, dovobet ointment should be applied to the affected area. In order to achieve optimal effect, it is not recommended to take a shower or bath immediately after application of dovobet ointment. 4.3 Contraindications, hypersensitivity to the active substances or to any of the excipients listed in section vobet is contraindicated in erythrodermic, exfoliative and pustular psoriasis. Due to the content of calcipotriol dovobet is contra-indicated in patients with known disorders of calcium metabolism (see section.4).due to the content of corticosteroid dovobet is contraindicated in the following conditions: Viral (e.g. Herpes or varicella) lesions of the skin, fungal or bacterial skin infections, parasitic infections, skin manifestations in relation to tuberculosis, perioral dermatitis, atrophic skin, striae atrophicae, fragility of skin veins, ichthyosis, acne vulgaris, acne rosacea, rosacea, ulcers and wounds (see section.4). 4.4 Special warnings and precautions for use.

Clinical particulars.1 Therapeutic indications. Topical treatment of stable plaque psoriasis vulgaris amenable to topical therapy in adults. 4.2 Posology and method of administration. Posology, dovobet ointment should be applied to the affected area once daily. The recommended treatment period is 4 weeks. There is experience with repeated courses of dovobet up to 52 weeks. If it is necessary to continue or restart treatment after 4 weeks, treatment should be continued after medical review and under regular medical supervision. When using calcipotriol containing medicinal products, the maximum daily dose should not exceed. The body surface area treated with calcipotriol containing medicinal products should not exceed 30 (see section.4).

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Dovobet Ointment - summary of Product Characteristics (SmPC) - (eMC). Skip to main content, start typing to retrieve search suggestions. When suggestions are available use up and down arrows to review and enter to select. Continue typing to refine. Advanced search back to top, active ingredient betamethasone dipropionate calcipotriol monohydrate. Legal Category, pOM: dior Prescription only medicine, this information is intended for use by health professionals. Name of the medicinal product. Dovobet 50 microgram/g.5 mg/g ointment. Qualitative and quantitative composition, one gram of ointment contains 50 micrograms of calcipotriol (as monohydrate) and.5 mg of betamethasone (as dipropionate).Excipient with known effects:Butylhydroxytoluene (E321) 50 micrograms/g ointmentFor the full list of excipients, see section.1.

Dovobet creme
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