Active substanceClotrimazoleClotrimazole
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  • Dosage form: & nbspspray for external use
    Composition:

    The 100 ml spray contains:

    Active substance: clotrimazole 1.00 g;

    Excipients: isopropyl myristate 2.50 g, macrogol 400 (Polyethylene glycol 400) 5.00 g,isopropanol (2-propanol) 72.10 g

    Description:From clear to slightly yellowish color transparent solution.
    Pharmacotherapeutic group:Antifungal agent
    ATX: & nbsp

    G.01.A.F.02   Clotrimazole

    Pharmacodynamics:

    Clotrimazole, the active substance of Kanesten® spray, is an imidazole derivative and has a broad spectrum of antimycotic action. The mechanism of action of clotrimazole is associated with inhibition of ergosterol synthesis, which leads to a disruption in the structure and functions of the cytoplasmic membrane of fungi. Has fungistatic or fungicidal activity depending on the concentration in the focus of infection.

    Kanesten® is active against dermatophytes, yeast-like, mold fungi, as well as the causative agent of a multicolored lichen (Pityriasis vers.) and the causative agent of erythrasma. Along with antimycotic, Kanesten® has an antimicrobial effect against Trichomonas vaginalis, Gram-positive (Streptococcus, Staphylococcus) and Gram-negative microorganisms (Bacteroides, Gardnerella vaginalis).

    In vitro in concentrations 0,5-10 mcg / ml clotrimazole suppresses the reproduction of the bacteria of the family Corynebacteria and Gram-positive cocci (excluding zinterococci) and has a trichomonaside effect at a concentration of 100 μg / ml.

    Primarily resistant strains of clotrimazole-sensitive fungi are very rare; the development of secondary resistance is observed only in individual cases and only under certain therapeutic conditions.

    Pharmacokinetics:

    Clotrimazole is practically not absorbed through intact and inflamed skin. The maximum concentration of clotrimazole in the blood plasma is below 0,001 μg / ml, which is confirmed by the fact that clotrimazole when applied topically to the skin does not lead to significant systemic side effects.

    Indications:

    Fungal skin diseases caused by dermatophytes, yeast-like fungi, mold fungi, as well as pathogens sensitive to clotrimazole:

    - fungal infections of feet, brushes, trunk, skin folds;

    - pityriasis lichen, erythrasma.

    Contraindications:

    Hypersensitivity to clotrimazole or other components of the drug.

    Carefully:Pregnancy and lactation.
    Pregnancy and lactation:

    Although it is not established that in the period of pregnancy and lactation Kanesten® spray has a negative effect on the mother and fetus, nevertheless, in the first 3 months of pregnancy and during lactation the drug can be used only after consulting a doctor.

    Dosing and Administration:

    Apply externally. Spray Kanesten ® spray a thin layer on the affected skin 2 times a day.

    The duration of therapy is individual and depends on the severity and localization of the disease. To achieve full recovery, do not stop spray treatment immediately after the disappearance of acute inflammation symptoms or subjective complaints. Duration of therapy should be about 4 weeks on average, after its completion (with the disappearance of clinical manifestations) it is advisable to continue treatment for another 14 days.

    Dermatomycoses are cured, mostly within 3-4 weeks, multi-colored lichen - 1-3 weeks.In fungal diseases of the skin of the legs, it is recommended to continue therapy for about 2-3 weeks after the relief of the symptoms of the disease. Before lubricating the feet wash with warm water and soap, carefully wipe, especially between the fingers.

    Side effects:

    Organism as a whole: allergic reactions; pain.

    Skin: local reactions (burning, swelling, irritation and peeling of the skin, paresthesia, erythematous rashes, the appearance of blisters).

    Overdose:The use of a spray in elevated doses does not cause any life reactions.
    Interaction:Amphotericin B, nystatin, natamycin reduce the effectiveness of clotrimazole while simultaneously using them.
    Special instructions:It is necessary to avoid getting on the mucous membrane of the eyes. When signs of hypersensitivity or irritation appear, the treatment is stopped. If there is no effect within 3 days, the diagnosis should be confirmed.
    Effect on the ability to drive transp. cf. and fur:Not visible.
    Form release / dosage:
    Spray for external use 1%.
    Packaging:To 30 ml in an opaque polyethylene bottle of white color, equipped with a pump dispenser and protective cap made of plastic; 1 bottle together with the instructions formedical use is placed in a cardboard box.
    Storage conditions:At a temperature not exceeding 25 °FROM.

    Keep out of the reach of children.

    Shelf life:3 years.

    Do not use after expiry date.

    Terms of leave from pharmacies:Without recipe
    Registration number:LS-001910
    Date of registration:13.06.2011 / 17.06.2016
    Expiration Date:Unlimited
    The owner of the registration certificate:BAYER, AO BAYER, AO Russia
    Manufacturer: & nbsp
    Representation: & nbspBAYER, AOBAYER, AO
    Information update date: & nbsp21.11.2017
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