Active substanceSodium chlorideSodium chloride
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  • Dosage form: & nbspsolvent for the preparation of dosage forms for injection.
    Composition:

    1 liter of solution contains:

    active substance: sodium chloride - 9 grams,

    adjuvant: water for injection - up to 1 liter.

    Description:

    Transparent colorless liquid.

    Pharmacotherapeutic group:Solvent
    ATX: & nbsp

    B.05.C.B.01   Sodium chloride

    B.05.X.A.03   Sodium chloride

    Pharmacodynamics:A solution of sodium chloride 0.9% is isotonic with human plasma.In small volumes it is used as a solvent for the preparation of injection solutions of drugs.
    Pharmacokinetics:It is excreted by the kidneys.
    Indications:

    Dissolution and dilution of drugs.

    Contraindications:

    Do not use to dissolve and dilute medicines for which another solvent is specified as mandatory.

    Pregnancy and lactation:The possibility of application during pregnancy and during breastfeeding is determined by the instruction for the use of that drug, for dilution of which a 0.9% solution of sodium chloride will be used.
    Dosing and Administration:

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

    Side effects:When using 0.9% sodium chloride solution as a drug solvent, the side effect profile depends on the basic drug.
    Overdose:When applying 0.9% sodium chloride solution as a drug solvent, the symptoms of overdose depend on the basic drug.
    Interaction:Compatible with colloid hemodynamic blood substitutes (mutual enhancement of the effect). When mixed with other drugs, you need to visually check for compatibility. To do this, it is necessary to observe the resulting solution to change its color and / or precipitate, the appearance of crystals, insoluble complexes. It is also necessary to take into account the instructions for the use of added drugs.
    Special instructions:

    Before dissolving / diluting the drug in an isotonic solution of sodium chloride, you should carefully read the instructions for use of the drug.

    Apply only a clear solution, with no visible inclusions and if the package is not damaged.The solution should be administered with the use of sterile equipment in compliance with the rules of aseptic and antiseptic. As with all parenteral solutions, the compatibility of the added substances with the solution should be determined before dissolution. Do not apply with 0.9% sodium chloride solution preparations known to be incompatible with it. Determine the compatibility of added drugs with a 0.9% sodium chloride solution should the doctor check the possible discoloration and / or the appearance of sediment, insoluble complexes or crystals. Before adding, it is necessary to determine whether the added substance is soluble and stable in water at the pH level as 0.9% sodium chloride solution. When adding the drug, it is necessary to determine the isotonicity of the solution obtained before administration. Before adding to the solution of the preparations, they must be thoroughly mixed in accordance with the rules of asepsis. Prepared solution should be introduced immediately after preparation, do not store! Do not freeze!

    Effect on the ability to drive transp. cf. and fur:

    Impact on the ability to perform potentially hazardous activities,requiring high concentration and psychomotor speed reactions (vehicle control, work with moving mechanisms) defined pharmacological effects and possible side effects of the basic drug, which is used for sodium chloride as a solvent for the preparation of solution for injection.

    Form release / dosage:

    Solvent for preparing dosage forms for injection, 0.9%.

    Packaging:

    For 2 ml, 5 ml, 10 ml in ampoules of polymeric or 2 ml, 4 ml in a tube of a dropper with a high-pressure polyethylene valve.

    10, 100 ampoules polymer with instructions for use placed in a pile of cardboard or polymeric vials 100 with instructions for use placed in a box made of cardboard.

    Packing "angro": 1200 tubes with the instructions for use are placed in a group package.

    Storage conditions:

    At a temperature of 15 ° C to 25 ° C.

    Keep out of the reach of children,

    Shelf life:

    5 years. Do not use after the expiration date.

    Terms of leave from pharmacies:On prescription
    Registration number:LSR-005762/08
    Date of registration:22.07.2008 / 25.10.2016
    Expiration Date:Unlimited
    The owner of the registration certificate:UPDATE OF PFC, CJSC UPDATE OF PFC, CJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp16.06.2018
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