Active substanceSodium chlorideSodium chloride
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  • Dosage form: & nbspinjection
    Composition:

    Active substance:

    Sodium chloride 0.009 mg

    Excipient:

    Water for injections up to 1 ml

    Theoretical osmolarity is 308 mOsmol / l.

    Description:

    Clear colorless liquid

    Pharmacotherapeutic group:solvent for the preparation of dosage forms for injection.
    ATX: & nbsp

    B.05.C.B.01   Sodium chloride

    B.05.X.A.03   Sodium chloride

    Pharmacodynamics:

    It is used as a solvent and serves for the preparation of injection solutions for subcutaneous,intramuscular or intravenous administration. Pharmacokinetics

    Sodium chloride is retained in the vascular bed for a short time. It is excreted by the kidneys unchanged.

    Indications:Dissolution and dilution of drugs.
    Contraindications:

    Sodium chloride solution for injection as a solvent medicinal products is not applied, if another solvent is indicated as mandatory for some of them.

    Carefully:not described
    Pregnancy and lactation:The drug is not contraindicated for use in pregnancy and lactation.
    Dosing and Administration:

    Subcutaneously, intramuscularly, intravenously after dissolution or dilution of drugs. Preparation of solutions of drugs using sodium chloride for injection is carried out under sterile conditions (opening ampoules, filling the syringe and containers with drugs). The route of administration and the amount of sodium chloride for injection used to prepare a solution of the drug are determined by the instruction for the use of the latter.

    Side effects:

    Acidosis, hyperhydration, hypokalemia (when administered in large amounts).

    When sodium chloride is used as a drug solvent, the side effect profile depends on the basic drug.
    Overdose:not described
    Interaction:

    When mixed with other drugs, visual compatibility checks are necessary (nevertheless, invisible and therapeutic incompatibility is possible).

    Special instructions:

    Possible freezing of the drug provided the container is hermetically sealed.

    Effect on the ability to drive transp. cf. and fur:Does not affect the reaction rate when driving vehicles and other mechanisms.
    Form release / dosage:

    Solution for injection 0.9%.

    Primary packaging. To 2, 5, 10 ml into polyethylene polyethylene of low density brand "Purell PE 3020 D" firms "Basell Sales & Marketing Company B.V." (Netherlands), or brands "Seetec BB120 "company "LG Chem" (South Korea), or from polyethylene for infusion and injection preparations in accordance with the requirements of the European Pharmacopoeia of the current edition.

    On ampoules paste labels from paper label, writing, for printing offset or imported.

    Secondary packaging. For 5 or 10 ampoules connected in cassettes with instructions for use are placed in a pack of cardboard for consumer packaging subgroups chrome or chromium-ersatz or other similar quality. The packets are placed in a shipping container.

    Packaging:ampoules polyethylene joined in cassettes (10) -tacks, cardboard
    ampoules polyethylene joined in cassettes (5) -tacks, cardboard
    Storage conditions:

    In the original packaging of the manufacturer at a temperature of 0 to 25 ° C. Keep away from children.

    Shelf life:

    5 years. Do not use after the expiry date printed on the package.

    Terms of leave from pharmacies:On prescription
    Registration number:LP-001960
    Date of registration:27.12.2012
    The owner of the registration certificate:FARMASINTEZ, JSC (Irkutsk) FARMASINTEZ, JSC (Irkutsk) Russia
    Manufacturer: & nbsp
    Information update date: & nbsp28.08.2013
    Illustrated instructions
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