Active substancePotassium chloridePotassium chloride
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  • Dosage form: & nbspconcentrate for solution for infusion
    Composition:

    1 ml of the solution contains:

    active substance: potassium chloride - 40 mg

    Excipients: dextrose monohydrate 334 mg hydrochloric acid (0.1 M hydrochloric acid solution) to pH 3,0-4,0 water for injection - up to 1 ml

    Description:Transparent colorless or slightly colored liquid.
    Pharmacotherapeutic group:Potassium preparation
    ATX: & nbsp

    B.05.X.A   Electrolyte solutions

    B.05.X.A.01   Potassium chloride

    Pharmacodynamics:

    Preparation K+, restores water-electrolyte balance. Has a negative chrono- and batmotropic effect, in high doses - negative foreign and dromotropic, as well as moderate diuretic effect. In small doses of K+ dilates coronary vessels, in large - narrows. Participates in the process of carrying out nerve impulses. With intravenous administration increases the secretion of epinephrine by the adrenal glands.

    Activates many cytoplasmic enzymes, participates in maintaining intracellular osmotic pressure, in protein-synthetic reactions and transport of amino acids. Improves the contraction of skeletal muscles in muscular dystrophy, myasthenia gravis. Increase in concentration of K+ reduces the risk of developing toxic effects of cardiac glycosides.

    Indications:

    Hypokalemia (incl.on the background of diabetes mellitus, prolonged diarrhea and / or vomiting, therapy with antihypertensive drugs, certain diuretics, glucocorticosteroids), treatment and prevention of digitalis intoxication, and the prevention of arrhythmia in patients with myocardial infarction (in acute period).

    Contraindications:

    Hyperkalemia, complete atrioventricular block, adrenal insufficiency, chronic renal failure, concomitant therapy with potassium-sparing diuretics, metabolic disorders (acidosis, hypovolemia with hyponatraemia), pregnancy, lactation, age under 18 years (efficacy and safety not established).

    Pregnancy and lactation:

    If necessary, use in pregnancy should be compared with the expected benefit for the mother and the potential risk to the fetus.

    During the lactation period, the issue of stopping breastfeeding should be addressed.

    Dosing and Administration:

    Intravenously. With hypokalemia with a violation of the heart rhythm - 1-1.5 g 4-5 times a day: after restoring the heart rhythm, the dose is reduced. With digitalis intoxication - 2-3 g / day, in severe cases - up to 5 g.To arrest seizures of paroxysmal tachycardia on the first day - 8-12 g, followed by a decrease to 3-6 g.

    Intravenously streamwise, if necessary intravenously drip (slowly, for 1 h) - 2-2.5 g in 500 ml of 5% dextrose solution. For the prevention and treatment of ectopic arrhythmias in myocardial infarction - a polarizing mixture: a solution of potassium chloride in a 5% - 10% solution of dextrose (add insulin at the rate of 1 unit for 3-4 g of dry dextrose).

    Side effects:

    From the nervous system: paresthesia, muscle weakness, confusion.

    From the side of the cardiovascular system: lowering of arterial pressure, arrhythmia, heart block, cardiac arrest.

    Other: hyperkalemia, allergic reactions.

    Overdose:

    Symptoms: hyperkalemia (muscle hypotension, paresthesia of the limbs, slowing of atrioventricular conduction, arrhythmias, cardiac arrest). Early clinical signs of hyperkalemia usually appear at a concentration of K+ in serum of blood more than 6 meq / l: sharpening of the tooth T, disappearance of the tooth U, segment decline ST, interval lengthening QT, expansion of the complex QRS. More severe symptoms of hyperkalemia - muscle paralysis and cardiac arrest - develop at a concentration of K+ 9-10 meq / L.

    Treatment: inside or intravenously - solution NaCl; intravenously - 300-500 ml of a 5% solution of dextrose (with 10-20 units of insulin in 1 liter); if necessary, hemodialysis and peritoneal dialysis.

    Interaction:

    Pharmaceutically compatible with solutions of cardiac glycosides (improves their tolerability).

    Strengthens the negative dromo - and Batmotropic effect of antiarrhythmic drugs.

    In the composition of the polarizing mixture (in combination with dextrose and insulin) contributes to the normalization of the heart rate with myocardial infarction, ectopic arrhythmias and an overdose of cardiac glycosides.

    Eliminates hypokalemia caused by glucocorticosteroids, mineralocorticosteroids and diuretics.

    Beta-blockers, ciclosporin, potassium-sparing diuretics, heparin, angiotensin-converting enzyme inhibitors, non-steroidal anti-inflammatory drugs may increase the risk of hyperkalemia.

    Special instructions:

    During the treatment period, it is necessary to control the K content+ in the blood serum, ECG, in the treatment of hypokalemia - control of the acid-base state.

    Safety and effectiveness of potassium chloride in children have not been established.

    A diet with a high content of sodium chloride increases the excretion of K+ from the body.

    It should be borne in mind that hyperkalemia, leading to death, can develop rapidly and proceed asymptomatically.

    Form release / dosage:

    Concentrate for the preparation of a solution for infusions 40 mg / ml.

    Packaging:

    10 ml per ampoule polymer from high-density polyethylene or from low-pressure polyethylene, or from polyethylene for medical purposes, or from polyethylene or polypropylene for infusion solutions and injections.

    For polymer ampoules, labels from label paper, writing or label text are applied directly to the ampoule by a polymer method of drop-jet printing.

    For 10, 100 ampoules of polymer with instructions for use are placed in a pack of cardboard.

    Storage conditions:

    At a temperature of 15 to 25 ° C.

    Keep out of the reach of children.

    Shelf life:

    3 years.

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

    Terms of leave from pharmacies:On prescription
    Registration number:LSR-008215/08
    Date of registration:17.10.2008 / 19.05.2015
    Expiration Date:Unlimited
    The owner of the registration certificate:UPDATE OF PFC, CJSC UPDATE OF PFC, CJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp20.11.2017
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