Disol (Disol)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Active substanceSodium acetate + Sodium chlorideSodium acetate + Sodium chloride
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    RESTER, CJSC     Russia
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    BIOSINTEZ, PAO     Russia
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    MOSFARM, LLC    
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    GROTEKS, LLC     Russia
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    NESVIZH FACTORY OF MEDICAL PREPARATIONS, RUP     Republic of Belarus
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    Kursk Biofactory - BIOK, FKP     Russia
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    DALHIMFARM, OJSC     Russia
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    KRASFARMA, JSC     Russia
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    • Dosage form: & nbspSolution for infusion.
    Composition:

    1 liter of the solution contains 6 g of sodium chloride, 2 g of sodium acetate, water for injection, up to 1 liter. Theoretical osmolarity: 235 mOsm / mol.

    Description:

    Transparent colorless liquid.

    Pharmacotherapeutic group:rehydrating agent
    ATX: & nbsp

    B.05.B.B.01   Electrolytes

    Pharmacodynamics:

    Disol has detoxication and hemodynamic effects, raises diuresis, improves rheological properties of blood.

    Pharmacokinetics:
    Indications:

    Disol is used as a remedy for correction of hyperkalemia and its consequences, with dehydration and intoxication of the organism, which occur in various diseases (acute dysentery, food current and co-infection, cholera El Tor (Inaba) and others).

    Contraindications:

    Hypersensitivity, renal and heart failure.

    Carefully:not described
    Pregnancy and lactation:not described
    Dosing and Administration:

    Disol solution is administered intravenously at a rate of 40 - 120 drops per minute. Before the introduction, it is heated to a temperature of 36-38 ° C.

    The drug is used under the control of laboratory testing before the electrolyte balance is normalized.

    The solution is administered in amounts necessary to replenish the volume of fluid lost with feces, vomit, urine and sweat. The balance of the injected fluid and diuresis is determined every 6 hours.

    Side effects:

    Allergic reactions, chills, swelling, tachycardia.

    Overdose:not described
    Interaction:not described
    Special instructions:

    It is necessary to monitor the indices of the input-electrolyte balance.

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

    Solution for infusions of 100, 250, 500 in polymeric containers. Containers of 70 pieces with a capacity of 100 ml, or 32 pieces with a capacity of 250 ml, or 20 pieces with a capacity of 500 ml, are placed in a box of corrugated cardboard with 3 to 5 instructions for use (for hospitals).

    Storage conditions:

    Store in a place protected from light and inaccessible to children at a temperature of no higher than 25 ° C. Short-term freezing of the drug during transportation (provided the container is tight) is not a contraindication to its use. After freezing, keep the containers in the shipping container at room temperature until completely thawed, before shaking, mix the solution in the container with shaking.

    Non-wetting of the inner surface of the container is not a contraindication to its use.

    Shelf life:2 years. Do not use after the expiration date.
    Terms of leave from pharmacies:On prescription
    Registration number:P N002007 / 01
    Date of registration:18.09.2009
    The owner of the registration certificate:RESTER, CJSC RESTER, CJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp18.09.2009
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