Nitrofungin-Teva® (Nitrofungin-Teva®)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Active substanceChlorinated nitrophenolChlorinated nitrophenol
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  • Nitrofungin-Teva®
    solution externally 
    Teva Pharmaceutical Enterprises Co., Ltd.     Israel
    • Dosage form: & nbspsolution for external use
    Composition:

    Active substance: chloronitrophenol - 1.0 g.

    Excipients: ethanol 96%, triethylene glycol, purified water - up to 100 ml.

    Description:

    Transparent, yellow to green-yellow solution with the smell of alcohol.

    Pharmacotherapeutic group:Antifungal agent
    ATX: & nbsp

    D.01.A.E   Other antifungal agents for external use

    Pharmacodynamics:

    Antifungal agent. At a solution concentration of 0.0001%, the growth Microsporum canis, Trichophyton gypseum; at a concentration of 0.0007% suppresses growth Candida albicans; when the content of the active substance is increased to 0.003%, it exhibits fungicidal action.

    At a higher concentration, it has antibacterial action against gram-positive and gram-negative bacteria.

    Indications:

    Fungal skin lesions: rubrophytic, inguinal epidermophytia, trichophytosis of skin candidiasis, foot fungal infections, fungal diseases of the external auditory canal.

    Contraindications:

    Hypersensitivity to the components of the drug.

    Pregnancy and lactation:

    Application in pregnancy is possible only in cases where the potential benefit to the mother exceeds the possible risk to the fetus. During the lactation period, it is necessary to resolve the issue of stopping breastfeeding.

    Dosing and Administration:

    Outwardly. The solution is applied to the affected skin with a cotton swab 2-3 times a day. Treatment continues until the disappearance of clinical manifestations of the disease.

    To prevent recurrence, the solution continues to be applied 2-3 times a week for 4-6 weeks. For the purpose of prophylaxis the solution is applied 1-2 times a week for 4 weeks

    Side effects:

    Local irritating effect, photodermatitis, allergic reactions.

    Interaction:

    Unknown.

    Special instructions:

    In case of severe irritant effects, a solution diluted with water (1: 1) can be used for daily use. Skin areas treated with the drug should not be exposed to sunlight.

    Form release / dosage:Solution for external use 1%.
    Packaging:To 25 ml of the drug in a bottle of brown glass, equipped with a dropper and a lid with the control of the first autopsy. Each vial with the instruction for use is placed in a cardboard box
    Storage conditions:

    At a temperature of 10 ° C to 25 ° C in the place protected from light. Keep out of the reach of children.

    Shelf life:

    5 years. Do not use after the expiration date.

    Terms of leave from pharmacies:Without recipe
    Registration number:П N012581 / 01
    Date of registration:17.08.2007 / 13.05.2014
    Expiration Date:Unlimited
    The owner of the registration certificate:Teva Pharmaceutical Enterprises Co., Ltd.Teva Pharmaceutical Enterprises Co., Ltd. Israel
    Manufacturer: & nbsp
    Representation: & nbspTeva Teva Israel
    Information update date: & nbsp23.06.2018
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