Active substanceSodium lactate solution is complex [Potassium chloride + Calcium chloride + Sodium chloride + Sodium lactate]Sodium lactate solution is complex [Potassium chloride + Calcium chloride + Sodium chloride + Sodium lactate]
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  • Dosage form: & nbspsolution for infusions
    Composition:

    Active substances:

    Sodium chloride - 6.00 g

    Potassium chloride - 0.40 g

    Calcium chloride hexahydrate - 0.27 g
    (in terms of anhydrous)

    Sodium lactate - 3.20 g

    Excipients: Water for Injection - up to 1.0 liter

    Ionic composition (per 1 liter):

    Sodium - ion - 131.0 mmol

    Potassium ion - 5.4 mmol

    Calcium ion - 1.8 mmol

    Chloride ion - 106.3 mmol

    Lactate ion - 28.5 mmol

    Theoretical osmolality 273 mOsmol / l
    Description:

    Transparent colorless liquid.

    Pharmacotherapeutic group:electrolyte balance is a restoring agent.
    ATX: & nbsp

    B.05.B.B.01   Electrolytes

    Pharmacodynamics:

    Rehydrating agent, has a detoxification effect Replenishes the deficiency of the volume of circulating blood, stabilizes the water and electrolyte composition of the blood.Normalizes the acid-base state. Lactate is metabolized in the body to bicarbonate, therefore the solution has alkalizing effect. The solution is close to isotonic, osmolarity is 273 mOsmol / l.

    Pharmacokinetics:
    Indications:

    Hypovolemia, isotonic dehydration, metabolic acidosis.

    Contraindications:Hypersensitivity, hypervolemia, hypertonic dehydration, hyperkalemia, hypernatremia, arterial hypertension, cardiac and / or renal insufficiency, hyperchloremia, alkalosis, hepatic insufficiency (decrease in the formation of bicarbonate from lactate), hyperlactacidemia.
    Carefully:Respiratory failure, acute dehydration, simultaneous treatment with glucocorticoid agents.
    Pregnancy and lactation:

    During pregnancy, apply in cases where the expected benefit to the mother exceeds the risk to the fetus. During lactation should refrain from breastfeeding.

    Dosing and Administration:

    Intravenously drip at a rate of 60 drops / min. At urgent conditions - 180 drops / min, in volume, depending on the patient's condition. Adults median daily dose - 1 liter, children - 20-30 ml / kg. The maximum daily dose is 2.5 liters.

    Side effects:

    Thrombophlebitis, hypervolemia, hyperhydration, hyperchloremia, anxiety, allergic reactions.

    Overdose:not described
    Interaction:

    Nonsteroidal anti-inflammatory drugs, androgens, anabolic steroids, estrogens, corticotropin, mineral corticosteroids, vasodilators and ganglion blockers increase the risk of hypernatremia; potassium-sparing diuretics, drugs K + - hypercapia. The drug becomes alkaline and inhibits the excretion of drugs that have an alkaline reaction. Accelerates excretion Li+ and salicipates.

    Special instructions:

    It is necessary to conduct a regular blood test to determine electrolytes, pH and partial pressure of CO2, the volume of circulating blood.

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

    Solution for infusion.

    200 or 400 ml in glass bottlesMTO brand for blood, transfusionand infusion drugs250, or 450 ml ofdirectly.

    1 bottle with instructions for medical application is placed in a pack of cardboard.

    For 28 bottles with a capacity of 250 or 15, bottles with a capacity of 450 ml with an equal number of instructions for medical use is placed in boxes of cardboard (for hospitals).

    Packaging:bottles for blood and blood substitutes (1) -tacks, cardboard
    bottles for blood and blood substitutes (1) - cardboard tacks (15)
    bottles for blood and blood substitutes (1) -package cardboard (28)
    bottles for blood and blood substitutes (15) - cardboard boxes
    bottles for blood and blood substitutes (28) - cardboard boxes
    Storage conditions:In the dark place at a temperature of no higher than 25 ° C. Keep out of the reach of children.
    Shelf life:

    2 years. Do not use after the expiration date printed on the package.

    Terms of leave from pharmacies:On prescription
    Registration number:LSR-005650/09
    Date of registration:14.07.2009
    The owner of the registration certificate:ESKOM NPK, OAO ESKOM NPK, OAO Russia
    Manufacturer: & nbsp
    Information update date: & nbsp30.06.2011
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