Composition, form of production and packaging
? Tablets of white color, flat-cylindrical, with a facet and a risk.
calcium gluconate monohydrate 500 mg
Auxiliary substances: potato starch 23 mg, talc 5 mg, calcium stearate monohydrate 2 mg.
10 pieces. - packings without cell contour (1) - packs cardboard.
10 pieces. - Packings without glue contour (2) - packs cardboard.
10 pieces. - packings of cellular contour (1) - packs cardboard.
10 pieces. - packings cellular planimetric (2) - packs cardboard.
INSTRUCTION FOR THE SPECIALIST.
Description of the drug approved by the manufacturer for the printed edition of 2011.
The preparation of calcium replenishes the deficiency of calcium ions necessary for the process of nerve impulse transmission, reduction of skeletal and smooth muscles, myocardial activity, bone formation, and blood clotting.
Approximately 1 / 5-1 / 3 part of the orally administered drug is absorbed into the small intestine; this process depends on the presence of vitamin D, pH, features of the diet and the presence of factors that can bind calcium ions. The absorption of calcium ions increases with its deficiency and the use of a diet with a reduced content of calcium ions. About 20% is excreted by the kidneys, the rest (80%) is removed from the intestinal contents.
Diseases accompanied by hypocalcemia, increased permeability of cell membranes (including blood vessels), impaired conduction of nerve impulses in muscle tissue.
Hypoparathyroidism (latent tetany, osteoporosis), metabolic disorders of vitamin D: rickets (spasmophilia, osteomalacia), hyperphosphatemia in patients with chronic renal failure.
The increased need for calcium ions (pregnancy, lactation period, the period of increased body growth), insufficient calcium ions in food, a violation of its metabolism (in the postmenopausal period).
Enhanced excretion of calcium ions (prolonged bed rest, chronic diarrhea, secondary hypocalcemia, long-term use of diuretics and antiepileptic drugs, glucocorticosteroids).
Poisoning with salts of magnesium ions, 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).
Hypercalcemic form of paroxysmal myoplegia.
Grind before consumption.
Inside, before meals or 1-1.5 hours after intake (squeezed milk). Adults - 1-3 g 2-3 times a day (the maximum daily dose - 9 g).
Pregnant and lactating mothers - 1-3 g 2-3 times a day (maximum daily dose - 9 g).
Children: 3-4 years - 1 g (maximum daily dose - 3.0 g); 5-6 years - 1-1.5 g (maximum daily dose - 4.5 g); 7-9 years - 1.5-2 g (the maximum daily dose - 6 g); 10-14 years - 2-3 g (the maximum daily dose - 9 g); the frequency of reception is 2-3 times a day.
Constipation, irritation of the mucous membrane of the gastrointestinal tract, hypercalcemia.
Hypersensitivity, hypercalcemia (concentration of calcium ions should not exceed 12 mg% ~ 6 mEq / L), expressed hypercalciuria, nefrourolitiaz (calcium), sarcoidosis, simultaneous reception of cardiac glycosides (risk of arrhythmias), children under 3 years.
Carefully. Dehydration, electrolyte disorders (risk of hypercalcemia), diarrhea, malabsorption syndrome, minor hypercalciuria, mild chronic renal failure, chronic heart failure, prevalent atherosclerosis, hypercoagulation, calcium nephrourolythiasis (in anamnesis).
PREGNANCY AND LACTATION
The application is possible according to the dosing regimen.
APPLICATION FOR FUNCTIONS OF THE LIVER
With caution: moderate chronic renal failure.
In patients with reduced glomerular filtration, treatment should be controlled by the concentration of calcium ions in the urine.
APPLICATION FOR CHILDREN
Contraindicated in children under 3 years.
In patients with minor hypercalciuria, a decrease in glomerular filtration or with nephrourolythiasis in history, treatment should be controlled by the concentration of calcium ions in the urine.
Drinking plenty is recommended to reduce the risk of nephrourolythiasis.
Symptoms: the development of hypercalcemia.
Treatment: Calcitonin is administered 5-10 IU / kg / day. (diluting it in 500 ml of 0.9% sodium chloride solution). Duration of administration 6 hours.
Forms insoluble complexes with antibiotics of the tetracycline series (reduces the antibacterial effect).
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.
TERMS OF RELEASE FROM PHARMACY
The drug is approved for use as a means of OTC.
TERMS AND CONDITIONS OF STORAGE
In a dry place, at a temperature of no higher than 25 В° C. Keep out of the reach of children.
Shelf life - 5 years. Do not use after the date shown on the package.