Active substanceDextroseDextrose
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  • Dosage form: & nbspsolution for infusions
    Composition:

    Active ingredient: dextrose monohydrate (in terms of anhydrous) 50 g or 100 g;

    auxiliary components: sodium chloride 0.26 g, 0.1 M hydrochloric acid solution to pH 3-4.1 (or up to pH 3-6), water for injection up to 1 liter.

    Description:A clear, colorless liquid.
    Pharmacotherapeutic group:Nutrition carbohydrate remedy
    ATX: & nbsp

    B.05.C   Irrigation solutions

    V.06.D   Other medications for nutrition

    V.04.C   Other diagnostic preparations

    Pharmacodynamics:
    Participates in various metabolic processes in the body. The infusion of dextrose solutions partially replenishes the water deficiency. Dextrose, entering the tissue, phosphorylated, turning into glucose-6-phosphate, which is actively included in many parts of the body's metabolism.

    5% dextrose solution is isotonic with blood plasma.

    10% hypertonic solution increases osmotic blood pressure, increases diuresis.

    Theoretical osmolarity of 10% dextrose is 555 mOsm / l.

    Pharmacokinetics:

    It is absorbed completely by the body, the kidneys are not excreted (the appearance in the urine is a pathological sign).

    Indications:

    Hypoglycemia, insufficiency of carbohydrate nutrition, toxicoinfection, intoxications in liver disease (hepatitis, dystrophy and atrophy of the liver, including hepatic insufficiency), hemorrhagic diathesis.

    As a component of various blood-substituting and anti-shock fluids: dehydration (vomiting, diarrhea, postoperative period); intoxication; collapse, shock.

    For the preparation of solutions of medicinal means for intravenous administration.

    Contraindications:

    Hypersensitivity, hyperglycemia, hyperhydration, diabetic coma, incl. hyperlactacidemia, postoperative disorders of glucose utilization; circulatory disorders that threaten edema of the brain and lungs; edema of the brain, pulmonary edema, acute left ventricular failure, hyperosmolar coma.

    Carefully:Decompensated chronic heart failure, chronic renal failure (oliguria, anuria), hyponatremia, diabetes, pregnancy and lactation.
    Dosing and Administration:

    Intravenously drip.

    5% (isotonic) solution of Glucose-E is administered at a maximum rate of up to 7 ml (150 cap / min or 400 ml / h); the maximum daily intake for adults is 2 liters; 10% (hypertonic) solution of Glucose-E - up to 60 cap / min (3 ml / min); the maximum daily intake for adults is 1 liter.

    In adults with a normal metabolism, the daily dose of dextrose administered should not exceed 4-6 g / kg, i.e. about 250-450 g (with a decrease in the metabolic rate, the daily dose is reduced to 200-300 g), while the daily volume of the injected liquid is 30-40 ml / kg.

    Children for parenteral nutrition, along with fats and amino acids, 6 g of dextrose / kg / day are administered on the first day, followed by up to 15 g / kg / day. To calculate the dose of dextrose with the administration of 5% and 10% solutions of Glucose-E, you must take into account the permissible volume of the injected fluid: for children with a body weight of 2-10 kg is 100-165 ml / kg / day, children with a body weight of 10-40 kg - 45-100 ml / kg / day.

    In the normal state of metabolism, the maximum rate of administration of Glucose-E adults - 0,25-0,5 g / kg / h (with a decrease in the intensity of the metabolism, the rate of administration is reduced to 0.125-0.25 g / kg / h). Children the rate of administration of Glucose-E should not exceed 0.5 g / kg / h; which is 5 ml of solution - about 10 ml / min or 200 cap / min (20 cap = 1 ml).

    For a more complete assimilation of dextrose, administered in large doses, concomitantly with it prescribe short-acting insulin at the rate of 1 unit of short-acting insulin for 4-5 g of dextrose.

    Patients with diabetes mellitus are administered dextrose under the control of its content in blood and urine.

    Side effects:Hypervolaemia, acute left ventricular failure.
    At the injection site - the development of infection, thrombophlebitis.
    Overdose:

    Symptoms: hyperglycemia, glucosuria, hyperglycemic hyperosmolar coma, hyperhydration, disturbance of water-electrolyte balance.

    Treatment: stop the introduction of Glucose-E, introduce short-acting insulin, symptomatic therapy.

    Interaction:

    When combined with other drugs, it is necessary to visually check compatibility (possible invisible pharmaceutical incompatibility).

    Special instructions:For a more complete and rapid assimilation of dextrose, it is possible to inject 4-5 units of insulin of short action subcutaneously, at the rate of 1 unit of short-acting insulin for 4-5 g of dextrose.
    Form release / dosage:Solution for infusions, 5% and 10%.
    Packaging:

    For 100, 200, 400 and 500 ml in glass bottles for blood, transfusion and infusion preparations with a capacity of 100, 250, 450 and 500 ml, respectively.

    For 100, 200, 250,400 and 500 ml in polymer bottles with a capacity of 100, 250 and 500 ml respectively.

    By 100, 250, 500 ml into polymeric containers for infusion solutions of single use.

    Each polyvinyl chloride container is placed in a bag of polyethylene film.

    For 1 bottle with instructions for medical use put in a pack of cardboard box.

    For 28 bottles with a capacity of 100 or 250 ml or 15 bottles with a capacity of 450 or 500 ml with an equal number of instructions for medical applications are placed in boxes of corrugated cardboard with gaskets and gratings "cores" of corrugated cardboard [for hospitals].

    For 72 containers or bags with a container of 100 ml capacity, 34 containers or bags with a 250 ml container or 22 containers or a 500 ml container bag with an equal number of instructions for medical use are placed in corrugated cardboard boxes [for hospitals].

    Storage conditions:

    In the dark place at a temperature of 2 to 25 ° C.

    Keep out of the reach of children.

    Shelf life:

    2 years.

    Do not use after the expiration date indicated on the package.

    Terms of leave from pharmacies:On prescription
    Registration number:P N003088 / 01
    Date of registration:17.03.2009 / 10.05.2012
    Expiration Date:Unlimited
    The owner of the registration certificate:ESKOM NPK, OAO ESKOM NPK, OAO Russia
    Manufacturer: & nbsp
    Representation: & nbspESKOM NPK, OAOESKOM NPK, OAO
    Information update date: & nbsp02.05.2017
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