Active substanceFluconazoleFluconazole
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  • Dosage form: & nbspgel for external use
    Composition:
    1 g of gel contains:
    Active substance: fluconazole 5.0 mg
    Excipients: propylene glycol 10 mg,methylparahydroxybenzoate -1.8 mg, propyl parahydroxybenzoate 0.2 mg, disodium edetate 0.5 mg, macrogol 400-50 mg, carbomer 10 mg, diethylamine to pH 6.0-7.0, water purified to 1.00 in

    Description:
    Colorless, opalescent, homogeneous gel

    Pharmacotherapeutic group:Antifungal agent.
    ATX: & nbsp

    J.02.A.C   Triazole derivatives

    J.02.A.C.01   Fluconazole

    Pharmacodynamics:
    Fluconazole belongs to the antifungal agents of the triazole group, it is a selective inhibitor of the synthesis of sterols in the membranes of the fungal cell, the mechanism of action is due to the blockade of cytochrome P-450.
    Active with opportunistic fungal infections, incl. caused by Candida spp. (including generalized forms of candidiasis on the background of immunodepression), Cryptococcus neoformans and Coccidioides immitis (including intracranial infections), Microsporum spp. and
    Active with opportunistic fungal infections, incl. caused by Candida spp. (including generalized forms of candidiasis on the background of immunodepression), Cryptococcus neoformans and Coccidioides immitis (including intracranial infections), Microsporum spp. and Trichophyton spp; with endemic mycoses caused by Blastomyces dermatidis, Histoplasma capsulatum (including with immunodepression).
    With local and external application is an antifungal drug of a wide spectrum of action. Has proven efficacy against microorganisms responsible for dermatomycosis,Pityriasis versicolor and cutaneous candidiasis (ie, Microsporum spp., Trichophyton spp., Epidermophyton spp., Candida spp. And Malassezia furfur or Pityrosporum orbiculata), as well as dermatophytes, yeast and mold fungi.

    Pharmacokinetics:
    When used externally, it is practically not absorbed from the surface of the skin and does not have a systemic effect.

    Indications:
    Treatment of superficial fungal infections of the skin, including foot mycoses (foot fungus), inguinal epidermophytic (tinea cruris), fungal lesions of the smooth skin of the body (tinea corporis); yeast infections of the skin (caused by Candida (eg, Candida albicans), in particular, intertrigo, colored lichen (Pityriasis versicolor), caused by Pityrosporum orbiculare.

    Contraindications:
    Hypersensitivity to the components of the drug (including other azole compounds in history), pregnancy (I trimester).

    Carefully:Pregnancy (II-III trimester), lactation.
    Dosing and Administration:
    Apply after consultation with your doctor!
    Apply externally: on the affected area of ​​the skin, apply the gel in a thin even layer, grasping also 2 cm and the adjacent area, and rub until completely absorbed 2 times a day (morning and evening). Duration of use within 1 - 3 weeks, depending on the pathogen and the place of its manifestation. Duration
    application - on the advice of a doctor.
    In some resistant forms, the duration of the application can be extended up to 6 weeks at the doctor's recommendation.

    Side effects:
    Rarely, local reactions can occur: skin irritation, burning sensation. Allergic reactions are possible (urticaria, skin rash).

    Overdose:
    There is no information.

    Interaction:
    Clinically significant drug interaction with Flukorem with other medications has not been established.

    Special instructions:
    The drug is not intended for use in ophthalmology.
    Avoid contact with the eyes. In the absence of the effect of therapy in the specified time, it is necessary to revise the diagnosis.
    When the first symptoms of hypersensitivity or skin irritation appear, the drug should be discarded. Without consulting a doctor, do not use with other medicines for topical use.

    Effect on the ability to drive transp. cf. and fur:
    The drug does not affect the ability to drive vehicles and work requiring increased concentration and speed of psychomotor reactions.

    Form release / dosage:
    Gel for external use 0,5%.
    Packaging:
    For 15 g or 30 g in a varnished, aluminum tube. Each tube together with the instruction for use is placed in a pack of cardboard.

    Storage conditions:
    In a dry, protected from light place at a temperature of no higher than 25 ° C.
    Keep out of the reach of children.

    Shelf life:
    2 years. Do not use after the expiration date.

    Terms of leave from pharmacies:Without recipe
    Registration number:LP-000601
    Date of registration:21.09.2011
    The owner of the registration certificate:REMEDIYA, LLC REMEDIYA, LLC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp28.09.2015
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