Active substanceCalcium gluconateCalcium gluconate
Similar drugsTo uncover
  • Calcium gluconate
    pills inwards 
    ATOLL, LLC     Russia
  • Calcium gluconate
    solution w / m in / in 
    ELLARA, LTD.     Russia
  • Calcium gluconate
    solution w / m in / in 
  • Calcium gluconate
    pills inwards 
  • Calcium gluconate
    solution w / m in / in 
    ATOLL, LLC     Russia
  • Calcium gluconate
    pills inwards 
  • Calcium gluconate
    pills inwards 
    URALBIOFARM, OJSC     Russia
  • Calcium gluconate
    pills inwards 
    BIOSINTEZ, PAO     Russia
  • Calcium gluconate
    solution w / m in / in 
    BINNOFARM, CJSC     Russia
  • Calcium gluconate
    solution w / m in / in 
    TRIM, LLC     Russia
  • Calcium gluconate
    pills inwards 
    LYUMI, LLC     Russia
  • Calcium gluconate
    pills inwards 
    UPDATE OF PFC, CJSC     Russia
  • Calcium gluconate
    solution w / m in / in 
    DALHIMFARM, OJSC     Russia
  • Calcium gluconate
    pills inwards 
    MEDISORB, CJSC     Russia
  • Calcium gluconate
    solution w / m in / in 
  • Calcium gluconate
    solution w / m in / in 
    ESKOM NPK, OAO     Russia
  • Calcium gluconate
    pills inwards 
    AVEKSIMA, JSC     Russia
  • Calcium gluconate
    solution w / m in / in 
  • Calcium gluconate
    solution w / m in / in 
    BIOSINTEZ, PAO     Russia
  • Calcium gluconate, stabilized
    solution for injections 
    FARMAK, PAO     Ukraine
  • Calcium gluconate, stabilized
    solution w / m in / in 
  • Calcium gluconate Extrabate
    pills inwards 
  • Calcium gluconate-Vial
    solution w / m in / in 
    VIAL, LLC     Russia
  • Calcium gluconate-lekT
    pills inwards 
  • Calcium gluconate-SOLOfarm
    solution w / m in / in 
    GROTEKS, LLC     Russia
  • Dosage form: & nbsppills
    Composition:1 tablet contains as active substance 500 mg of calcium gluconate; Excipients: potato starch - 12.51 mg, talcum - 13.25 mg, calcium stearate - 4.24 mg.
    Description:Tablets of white color, flat-cylindrical form with a risk and a facet.
    Pharmacotherapeutic group:Calcium-phosphorus exchange regulator
    ATX: & nbsp

    A.12.A.A.03   Calcium gluconate

    A.12.A.A   Calcium preparations

    Pharmacodynamics:

    The preparation of calcium replenishes calcium deficiency, which is necessary for the process of nerve impulse transmission, reduction of skeletal and smooth muscles, myocardial activity, bone formation, blood coagulation.

    Pharmacokinetics:

    Approximately 1 / 5-1 / 3 part of the orally administered drug is absorbed into the small intestine; this process depends on the presence of the vitamin D, pH, dietary characteristics and the presence of factors that are able to bind calcium. The absorption of calcium increases with its deficiency and the use of a diet with a reduced content of calcium. About 20% is excreted by the kidneys, the rest (80%) by the intestine.

    Indications:

    Hypoparathyroidism (latent tetany, osteoporosis).

    Violation of the metabolism of the vitamin D: rickets (spasmophilia, osteomalacia), hyperphosphatemia in patients with chronic renal insufficiency.

    Increased need for calcium (pregnancy, lactation, a period of increased body growth), insufficient calcium in the diet, a violation of its metabolism (in the postmenopausal period).

    Enhanced excretion of calcium (prolonged bed rest, chronic diarrhea, secondary hypocalcemia, long-term use of diuretics and antiepileptic drugs, glucocorticosteroids).

    Poisoning with magnesium salts, oxalic and fluoric acids and their soluble salts (in the interaction with calcium gluconate insoluble and non-toxic calcium oxalate and calcium fluoride are formed).

    Hyperkaliemic form of paroxysmal myoplegia.

    Contraindications:

    Hypersensitivity to the components of the drug, hypercalcemia (calcium concentration should not exceed 12 mg% = 6 mEq / L), expressed hypercalciuria, nephrourolythiasis (calcium), severe renal failure, sarcoidosis, simultaneous reception of cardiac glycosides (risk of arrhythmias), childhood to 3 years.

    Carefully:

    Dehydration, electrolyte disorders (risk of hypercalcemia), diarrhea, malabsorption syndrome, calcium nephrourolythiasis (in the anamnesis), minor hypercalciuria, moderate chronic renal failure, chronic heart failure, prevalent atherosclerosis, hypercoagulation.

    Pregnancy and lactation:The use of the drug is permissible taking into account the ratio of the benefits for the woman / risk to the fetus (child), which is determined by the doctor. When taking calcium supplements during breastfeeding, it is possible to penetrate into breast milk.
    Dosing and Administration:

    Inside, before meals or 1-1.5 hours after taking (squeezed milk).

    Doses are determined by the attending physician individually depending on the clinical picture.

    Hypoparathyroidism (latent tetany, osteoporosis): adults 1-3 g 2-3 times a day; children 3-4 years old - 1 g; 5-6 years - 1-1.5 g; 7-9 years - 1.5-2 g; 10-14 years - 2-3 g; the frequency of admission is 2-3 times a day.

    Violation of the metabolism of the vitamin D: rickets (spasmophilia, osteomalacia), hyperphosphatemia in patients with chronic renal failure: adults 1-3 g 2-3 times a day; children 3-4 years old - 1 g; 5-6 years - 1-1.5 g; 7-9 years - 1.5-2 g; 10-14 years - 2-3 g; the frequency of admission is 2-3 times a day.

    The increased need for calcium (pregnancy, lactation, a period of increased body height), insufficient calcium in food, a violation of its metabolism: adults 1-3 g 2-3 times a day; children 3-4 years old - 1 g; 5-6 years - 1-1.5 g; 7-9 years - 1.5-2 g; 10-14 years - 2-3 g; the frequency of admission is 2-3 times a day.

    Enhanced excretion of calcium (prolonged bed rest, chronic diarrhea, secondary hypocalcemia, long-term use of diuretics and antiepileptic drugs, glucocorticosteroids): adults 1-3 g 2-3 times a day; children 3-4 years old - 1 g; 5-6 years - 1-1.5 g; 7-9 years - 1.5-2 g; 10-14 years - 2-3 g; the frequency of admission is 2-3 times a day.

    Poisoning with magnesium salts, oxalic and fluoric acids and their soluble salts: adults 1-3 g 2-3 times a day; children 3-4 years old - 1 g; 5-6 years - 1-1.5 g; 7-9 years - 1.5-2 g; 10-14 years - 2-3 g; the frequency of admission is 2-3 times a day.

    Hyperkalemic form of paroxysmal myoplegia: adults 1-3 g 2-3 times a day; children 3-4 years old - 1 g; 5-6 years - 1-1.5 g; 7-9 years - 1.5-2 g; 10-14 years - 2-3 g; the frequency of admission is 2-3 times a day.

    Side effects:Constipation, irritation of the mucous membrane of the gastrointestinal tract, hypercalcemia.
    Overdose:

    Symptoms: hypercalcemia (drowsiness, weakness, anorexia, abdominal pain, vomiting, nausea, constipation, polydipsia, polyuria, fatigue, irritability, poor health, depression, dehydration, possible heart rhythm disturbance, myalgia, arthralgia, arterial hypertension).

    Treatment: drug cancellation; in severe cases - parenterally calcitonin in a dose of 5-10 IU / kg body weight per day (when diluted in 500 ml sterile 0.9% saline solution of sodium chloride), intravenously drip for 6 hours. Intravenous jet slow injection 2-4 times a day is possible.

    Interaction:

    Pharmaceutically incompatible with carbonates, salicylates, sulfates (forms insoluble or hardly soluble calcium salts).

    Forms insoluble complexes with antibiotics of the tetracycline series (reduces the antibacterial effect).

    Reduces the effect of blockers of "slow" calcium channels.

    With simultaneous application with quinidine, it is possible to slow intraventricular conduction and increase the toxicity of quinidine.

    Slows the absorption of tetracyclines, digoxin, oral iron preparations (the interval between their methods should be at least 2 hours).

    When combined with thiazide diuretics can increase hypercalcemia. Reduces the effect of calcitonin in hypercalcemia.

    Reduces the bioavailability of phenytoin.

    Special instructions:

    In patients with minor hypercalciuria, reduced glomerular filtration or with nephrourolythiasis in history, treatment should be controlled by the concentration of calcium in the urine.

    Drinking plenty is recommended to reduce the risk of nephrourolythiasis.

    Effect on the ability to drive transp. cf. and fur:

    The drug does not affect the driving of vehicles and the management of mechanisms.

    Form release / dosage:Tablets 500 mg.
    Packaging:

    For 10 tablets in a contiguous, non-jawed package or a contiguous cell package.For 1 or 2 contour mesh packages along with the instruction for use are placed in a pack of cardboard. It is allowed to pack outline packages together with an equal number of instructions for use in a group package.

    Storage conditions:

    At a temperature of no higher than 25 ° C. Keep out of the reach of children.

    Shelf life:

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

    Terms of leave from pharmacies:Without recipe
    Registration number:LS-002454
    Date of registration:30.12.2011
    Expiration Date:Unlimited
    The owner of the registration certificate:TATHIMFARMPREPARATY, JSC TATHIMFARMPREPARATY, JSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp23.11.2017
    Illustrated instructions
      Instructions
      Up