Active substancePotassium chloride + Sodium acetate + Sodium chloridePotassium chloride + Sodium acetate + Sodium chloride
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  • Dosage form: & nbspsolution for infusions
    Composition:

    sodium chloride - 5 g

    potassium chloride - 1 g

    sodium acetate trihydrate - 2 g

    water for injection up to -1 l.

    Description:Colorless transparent liquid.
    Pharmacotherapeutic group:Rehydrating agent
    ATX: & nbsp

    B.05.B.B.01   Electrolytes

    Pharmacodynamics:

    Combined saline solution for rehydration and detoxification. Has a hemodynamic effect, reducing hypovolemia,interfering with blood thickening and development of metabolic acidosis, improves capillary blood circulation, increases diuresis and exerts detoxification effect.

    Indications:

    Rehydration, intoxication on the background of dehydration (including cholera, acute dysentery, food toxicoinfection).

    Contraindications:Hypersensitivity, hyperkalemia, renal and heart failure, alkalosis.
    Carefully:Not described.
    Pregnancy and lactation:Not described.
    Dosing and Administration:Intravenously (struino and drip), under the control of laboratory indicators. Within 1 hour, inject a solution in an amount corresponding to 7-10% of the body weight of the patient; then the jet infusion is replaced by a dropwise addition, for 24-48 hours at a rate of 40-120 cap / min. Before administration, the solution is heated to 36-38 ° C. The solution is administered in amounts necessary to restore the volume of fluid lost with feces, vomit, urine, sweat. The balance of injected and lost fluid is determined every 6 hours
    Side effects:

    Edema, tachycardia, hyperkalemia. Rarely - chills.

    Overdose:Not described.
    Interaction:Not described.
    Special instructions:

    Therapy is carried out under the control of hematocrit and the concentration of blood electrolytes.

    With the development of hyperkalemia, the solution can be replaced with a solution of "Disol" until the electrolyte balance is normalized.

    Non-wetting of the inner surface of bottles is not a contraindication to the use of the drug.

    Effect on the ability to drive transp. cf. and fur:Not described.
    Form release / dosage:

    Solution for infusion.

    Packaging: In glass bottles for blood, transfusion and infusion preparations of 200 and 400 ml. For hospitals - 40 bottles of 200 ml, 24 bottles of 400 ml, along with 10-15 instructions for use in a cardboard box.
    Storage conditions:At a temperature not higher 25 ° С in places inaccessible to children. Freezing of the drug is not a contraindication to its use, provided the packaging is hermetically sealed. Non-wetting of the inner surface of bottles is not a contraindication to the use of the drug.
    Shelf life:2 of the year. Do not apply at the expiration date indicated on the package.
    Terms of leave from pharmacies:On prescription
    Registration number:П N015752 / 01
    Date of registration:18.05.2009
    Expiration Date:Unlimited
    The owner of the registration certificate:NESVIZH FACTORY OF MEDICAL PREPARATIONS, RUP NESVIZH FACTORY OF MEDICAL PREPARATIONS, RUP Republic of Belarus
    Manufacturer: & nbsp
    Information update date: & nbsp03.10.2017
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