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Daivonex® scalp solution Jogosultság Kritériumok: Inclusion Criteria: 1. Signed and dated informed consent has been obtained. Subjects of either gender 18 years of age or above.

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Female of childbearing potential using a reliable method of contraception for at least 1 month before the trial start and during the course of mild psoriasis face trial e.

Exclusion Criteria: 1.

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Current diagnosis of guttate, erythrodermic, exfoliative, or pustular psoriasis. Mild psoriasis face with any of the following conditions present on the scalp area: viral lesions, fungal and bacterial skin infections, parasitic infections, hajnali kenőcs pikkelysömör vélemények manifestations in relation to syphilis or tuberculosis, rosacea, acne vulgaris, acne rosacea, atrophic skin, striae atrophicae, fragility of skin veins, ichthyosis, ulcers, and wounds.

Systemic treatment with all other therapies with a possible effect on psoriasis vulgaris e.

Lotion clear skin from psoriasis reviews Betametazon dipropionate lotion pikkelysömör Teersalbe a máj pszoriázisa Pikkelysömör elleni fluprednidene kezelés Plantes Garra best lotion for psoriasis on face hal psoriasis képek Ukrán klinikákon pikkelysömör kezelésére Ecologie et biodiversité Jardin, météo et Lune Amevive psoriasis oscar. Betamethasone is a steroid medication. Betamethasone diproprionate is a type of medicine called a corticosteroid. A pikkelysömör kezelése népi gyógymódokkal A népi gyógymódok a pszoriázisra Betamethasone Dipropionate for prescription cream called Betamethasone.

PUVA therapy within 4 weeks prior to randomisation or during the trial. UVB therapy within 2 weeks prior to randomisation or during the trial.

Therapies within 2 weeks prior to randomisation and during the trial: - Topical treatment of body psoriasis with very potent WHO group IV corticosteroids - Topical treatment of face psoriasis with potent or very potent WHO group III and IV corticosteroids - Any topical treatment of the scalp except for non-steroid medicated shampoos and emollients 8.

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Known or suspected renal insufficiency or hepatic disorders or severe heart disease. Clinical signs or symptoms of Cushing's disease or Addison's disease.

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Known or suspected hypersensitivity to component s of IMPs Current participation in any other interventional clinical trial Subjects who have received treatment with any non-marketed drug substance i. Previously participated in a clinical trial within 4 weeks prior to randomisation.

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In the opinion of the sub investigator, the subject is unlikely to comply with the clinical trial protocol e. Females who are pregnant, or of child-bearing potential and wish to become pregnant during the trial, or who are breast-feeding. Females of child-bearing potential with a positive urine pregnancy test at visit 1.

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