Active substanceSodium chlorideSodium chloride
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  • Dosage form: & nbsp

    solvent for the preparation of dosage forms for injections

    Composition:

    1 ml of the preparation contains: active substance: sodium chloride - 9 mg auxiliary substance: water for injection - up to 1 ml.

    Description:Clear colorless liquid
    Pharmacotherapeutic group:solvent
    ATX: & nbsp

    B.05.C.B.01   Sodium chloride

    B.05.X.A.03   Sodium chloride

    Pharmacokinetics:
    Indications:Dissolution and dilution of drugs.
    Contraindications:

    Sodium chloride solvent for the preparation of dosage forms for injection 0.9% as a solvent for medicinal products is not applicable, if another solvent is specified as mandatory for some.

    Carefully:not described
    Pregnancy and lactation:

    The possibility of application during pregnancy and during breastfeeding is determined by the properties of the drug, for dissolution or dilution of which a solvent was used.

    Dosing and Administration:

    Subcutaneously, intramuscularly, intravenously after dissolution or dilution of drugs. Preparation of drug solutions using sodium chloride solvent for the preparation of medicinal forms for injection 0.9% is carried out under sterile conditions (opening the ampoule, filling the syringe and containers with drugs). The quantity of sodium chloride of the solvent for the preparation of medicinal forms for injection 0.9% for the purpose of preparing a solution of a specific agent is determined by the instruction for the use of the latter or, depending on the situation, by the doctor.

    Side effects:

    Side effects are determined by the side effects of the drug, for dissolution or dilution of which a solvent was used.

    Overdose:not described
    Interaction:

    When mixed with other drugs, it is necessary to visually check compatibility (nevertheless, invisible and therapeutic incompatibility is possible).

    Special instructions:not described
    Effect on the ability to drive transp. cf. and fur:

    The effect on the ability to control vehicles, mechanisms is determined by the properties of the drug, for dissolution or dilution of which a solvent was used.

    Form release / dosage:Solution for injection 0.9% in ampoules of 1 ml, 2 ml, 5 ml or 10 ml.
    Packaging:For 10 ampoules with instructions for use, with an ampoule or ampoule ampoule knife in a pack or box of cardboard.
    5 ampoules in the outline of the cell. 2 contour packs with instructions for use, ampoule or ampoule with a knife in a pack of cardboard. When packaging ampoules that have a break ring or an opening point, the ampoule knife or the ampoule scapegrator is not put in.
    5 ampoules in a cassette outline package. 2 cassette contour packs with instructions for use in a pack of cardboard. It is possible to complete with dry dosage forms of drugs in appropriate quantities.
    Storage conditions:

    Store at a temperature not exceeding 25 ° C. Keep out of the reach of children.

    Shelf life:

    Shelf life 5 years. Do not use after the expiration date printed on the package.

    Terms of leave from pharmacies:On prescription
    Registration number:P N002009 / 01
    Date of registration:17.03.2008
    The owner of the registration certificate:MICROGEN FGUP Scientific and Production Association MICROGEN FGUP Scientific and Production Association Russia
    Manufacturer: & nbsp
    Information update date: & nbsp30.07.2015
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