Active substanceDextrose + Potassium chloride + Sodium chloride + Sodium citrateDextrose + Potassium chloride + Sodium chloride + Sodium citrate
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  • Hydrovit®
    powder inwards 
  • Hydrovit® forte
    powder inwards 
  • Regidron
    powder inwards 
  • Trigidron®
    powder inwards 
    MARBIOFARM, OJSC     Russia
  • Dosage form: & nbspPowder for solution for oral administration
    Composition:

    One packet contains:

    active ingredients: glucose anhydrous 4.00 g, sodium citrate dihydrate 0.59 g, sodium chloride 0.70 g, potassium chloride 0.30 g;

    auxiliary ingredients: flavor of lemon 0.04 g, flavor of natural black tea 0.16 g, sodium saccharin 0.02 g, D.L. malic acid 0.20 g, dry dye (E 150) 0.02 g.

    Total weight 6.03 g.

    Description:

    Powder of light brown color.

    Pharmacotherapeutic group:Rehydrating agent for oral administration
    ATX: & nbsp

    A.07.C.A   Rehydrate for oral use

    Pharmacodynamics:

    The therapeutic effect of the drug is due to the increase in the volume of circulating blood, the restoration of disturbed electrolyte equilibrium and the correction of acidosis.

    Indications:Dehydration and electrolyte balance disorders in complex treatment for diarrhea of ​​various origins.

    Caveats:

    Diarrhea can be a sign of a serious illness (including infectious disease). If diarrhea does not go away within 2-3 days and / or if the general condition worsens, you should consult a doctor without delay.

    Usually in infants and young children, diarrhea, especially accompanied by constant vomiting, can lead to serious symptoms (loss of consciousness, shock). Therefore, always consult with your doctor before starting treatment of diarrhea in infants and young children.

    Contraindications:

    - Acute or chronic renal failure;

    - Mr.vomiting;

    - Ploss of consciousness and shock in case of acute lack of fluid;

    - metabolic alkalosis;

    - a violation of the assimilation of carbohydrates in the intestine (congenital monosaccharide malabsorption).

    Carefully:

    Heart failure, arterial hypertension, diabetes mellitus.

    Pregnancy and lactation:

    Data are not available, as no special studies have been conducted.

    Dosing and Administration:

    For oral administration, after dissolving the contents of one Hydrovita® forte bag in 200 ml of drinking water. In the absence of drinking water, freshly boiled chilled water or tea can be used.

    The dosage of Hydrovita® forte depends on the severity of the patient's condition.

    The total volume of the final solution taken for 24 hours for patients with moderate to moderate diarrhea with a low degree of dehydration (loss of less than 5% of weight) is:

    Infants: from 100 to 150 ml / kg of body weight

    Dyoung children: from 80 to 120 ml / kg body weight

    Children of school age: from 50 to 80 ml / kg of body weight

    Older children and adults: from 20 to 60 ml / kg of body weight

    The above doses are of an advisory nature. Some patients may need smaller or larger doses.

    Elevated doses may be useful at the beginning of treatment for rapid and complete recovery of fluid loss.

    One packet of this preparation contains 4 g of glucose. According to the instructions, each dose can contain up to 3 g of glucose / kg of body weight.

    Patients with nausea and / or vomiting should begin treatment with a small amount of solution - 5-10 ml each 5-10 minutes, increasing the amount of the solution taken, according to the clinical condition, to the recommended dose.

    Breast-fed infants should first be given the recommended amount of Hydrovit® forte dissolved powder and then fed.

    Duration of treatment

    Treatment with the drug Hydrovit® forte should be continued while diarrhea lasts.

    Side effects:

    Irritation of the stomach, due to the presence of potassium, can cause nausea and vomiting.

    Overdose:

    Hyperhydration, electrolyte balance disorders, hyperglycemia.

    Accidental intoxication with undiluted powder can disrupt electrolyte balance and increase diarrhea.

    Interaction:

    The action of cardiac glycosides can be weakened. In patients undergoing treatment with glycosides, it is necessary to monitor the concentration of potassium in the blood.

    Special instructions:

    You can not boil the solution of Hydrovit® Fort.

    It is necessary to dissolve Hydrovit® forte strictly in the specified amount of liquid. The solution in a lower concentration does not contain the optimal amount of electrolytes and glucose, while a solution with a higher concentration may cause electrolyte imbalance in the body.

    The solution for oral administration should be prepared immediately before use. At room temperature, the ready-to-use solution is stable for 1 hour.

    When stored in a refrigerator, the solution is stable for no more than 24 hours.

    All unused portions of the solution must be destroyed.

    Patients with diabetes should bear in mind that one sachet of the drug Hydrovit® forte contains 4 g of glucose. The concentration of glucose in the finished solution for oral administration: 111 mmol / l.

    The concentration of electrolytes in the ready-mixed oral solution:

    - Sodium ions 90 mmol / l (60 from sodium chloride + 30 from citrate),

    - Potassium ions 20 mmol / l,

    - Chloride ions 80 mmol / l (60 from sodium chloride + 20 from potassium chloride),

    - Citrate ions 10 mmol / l.

    Theoretical osmolarity of the ready solution for oral administration: 311 mOsm / l.

    Form release / dosage:Powder for solution for oral administration.
    Packaging:

    In a bag made of a combination film material of 6.03 grams

    For 10 and 20 bags together with instructions for medical use of the drug are placed in a pack of cardboard.

    Storage conditions:

    In a place inaccessible to children, at a temperature of no higher than 25 ° C.

    Shelf life:

    5 years.

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

    Terms of leave from pharmacies:On prescription
    Registration number:LSR-001926/08
    Date of registration:18.03.2008
    Expiration Date:Unlimited
    Date of cancellation:2017-08-29
    The owner of the registration certificate:SHTADA Artznajmittel AGSHTADA Artznajmittel AG Germany
    Manufacturer: & nbsp
    Representation: & nbspNizhpharm, JSCNizhpharm, JSCRussia
    Information update date: & nbsp29.08.2017
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