Active substanceAscorbic acidAscorbic acid
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  • Dosage form: & nbsppills
    Composition:

    Composition per one pellet

    Ascorbic acid (vitamin C) - 50.0 mg.

    Excipients: sucrose -177.5 mg, starch syrup - 7.2 mg, wheat flour - 15.0 mg, sunflower oil -0.05 mg, beeswax-0.04 mg, talc-0.14 mg, orange flavoring - 0.02 mg, dye quinoline yellow - 0.05 mg.

    Description:

    The dragees are greenish-yellow or yellow in regular spherical shape. The surface of the dragee should be smooth, smooth, uniform in color.

    Pharmacotherapeutic group:Vitamin
    ATX: & nbsp

    A.11.G.A.01   Ascorbic acid

    Pharmacodynamics:

    Ascorbic acid actively participates in many oxidation-reduction reactions, it has a nonspecific general stimulating effect on the body. Increases the adaptive abilities of the body and its resistance to infections; promotes regeneration processes.

    Indications:

    Prevention and treatment of hypo- and vitamin deficiency vitamin C.

    As an auxiliary: hemorrhagic diathesis, nasal, uterine, pulmonary and other bleeding, against the background of radiation sickness; overdose of anticoagulants, infectious diseases and intoxications, liver disease, nephropathy of pregnant women, Addison's disease, sluggishly healing wounds and fractures of brachi, dystrophies and other pathological processes. The drug is prescribed for increased physical and mental stress, during pregnancy and breastfeeding, during recovery from severe long-term illnesses.

    Contraindications:

    Hypersensitivity to the components of the drug, thrombophlebitis, a tendency to thrombosis, diabetes mellitus.

    Carefully:

    Hyperoxalaturia, renal failure, hemochromatosis, thalassemia, polycythemia, leukemia, sideroblastic anemia, glucose-6-phosphate dehydrogenase deficiency, sickle-cell anemia, progressive malignant diseases, pregnancy.

    Pregnancy and lactation:

    The minimum daily requirement for ascorbic acid in II-III trimesters of pregnancy - about 60 mg.

    The minimum daily requirement for breastfeeding is 80 mg. A mother's diet containing an adequate amount of ascorbic acid is sufficient to prevent the deficiency of vitamin C in an infant (it is recommended not to exceed the maximum daily requirement for ascorbic acid by the nursing mother).

    Dosing and Administration:

    The drug is taken orally after a meal.

    For prophylaxis: adults 0.05-0.1 g (1-2 tablets) a day, children from 5 years of 0.05 g (1 tablet) per day.

    For treatment: adults 0.05-0.1 g (1-2 tablets) 3-5 times a day, children from 5 years of 0.05-0.1 grams (1-2 tablets) 2-3 times a day day.

    During pregnancy and breastfeeding, 0.3 g (6 tablets) a day for 10-15 days, then 0.1 g (2 tablets per day) per day.

    Side effects:

    From the central nervous system (CNS): headache, fatigue, with prolonged use of large doses - increased excitability of the central nervous system, sleep disturbances.

    From the digestive system: irritation of the gastrointestinal mucosa, nausea, vomiting, diarrhea, stomach cramps.

    From the endocrine system: oppression of the function of the insular apparatus pancreas (hyperglycemia, glucosuria).

    From the urinary system: when used in high doses - hyperoxalaturia and the formation of urinary stones from calcium oxalate.

    From the side of the cardiovascular system: thrombosis, when used in high doses - increased blood pressure, development of microangiopathies, myocardial dystrophy.

    Allergic reactions: skin rash, rarely - anaphylactic shock.

    Laboratory indicators: thrombocytosis, hyperprothrombinemia, erythropenia, neutrophilic leukocytosis, hypokalemia.

    Other: hypervitaminosis, a feeling of heat, with prolonged use of large doses - sodium retention (Na+) and fluids, the disruption of zinc metabolism (Zn2+), copper (Cu2+).

    Overdose:

    When taking more than 1 g per day, heartburn, diarrhea, difficulty urinating or staining the urine red, hemolysis (in patients with deficiency of glucose-6-phosphate dehydrogenase) are possible.

    If any side effects occur, stop taking the medication and consult a doctor.

    Interaction:

    Increases the concentration in the blood of benzylpenicillin and tetracyclines; in a dose of 1 g / day increases the bioavailability of ethinyl estradiol.

    Improves absorption in the intestines of iron preparations (converts trivalent iron into bivalent); can increase the excretion of iron with simultaneous application with deferoxamine.

    Acetylsalicylic acid (ASA), oral contraceptives, fresh juices and alkaline drink reduce absorption and absorption.

    With simultaneous application with ASA, urinary excretion of ascorbic acid increases and ASA excretion decreases. ASA reduces the absorption of ascorbic acid by about 30%.

    Increases the risk of developing crystalluria in the treatment of salicylates and sulfonamides short-acting, slows the excretion of kidney acids, increases the excretion of drugs that have an alkaline reaction (including alkaloids), reduces the concentration of oral contraceptives in the blood.

    Increases the total clearance of ethanol, which, in turn, reduces the concentration of ascorbic acid in the body.

    Preparations of quinoline series (fluoroquinolones, etc.), calcium chloride, salicylates, glucocorticosteroids with long-term use deplete the stores of ascorbic acid.

    With simultaneous use reduces the chronotropic effect of isoprenaline.

    With prolonged use or use in high doses, it can disrupt the interaction of disulfiram-ethanol.

    In high doses increases the renal excretion of mexiletine.

    Barbiturates and primidon increase the excretion of ascorbic acid in the urine.

    Reduces the therapeutic effect of antipsychotic agents (phenothiazine derivatives), tubular reabsorption of amphetamine and tricyclic antidepressants.

    Special instructions:

    In connection with the stimulating effect of ascorbic acid on the synthesis of corticosteroid hormones, it is necessary to monitor the kidney function and arterial pressure.

    With prolonged use of large doses, oppression of the insulin function of the pancreas is possible, so during treatment it must be regularly monitored.

    In patients with elevated iron levels in the body, ascorbic acid should be used in minimal doses.

    Assigning ascorbic acid to patients with rapidly proliferating and intensely metastatic tumors can aggravate the course of the process.

    Ascorbic acid, as a reducing agent, can distort the results of various laboratory tests (blood glucose, bilirubin, transaminase activity, LDH).

    Form release / dosage:Dragee.
    Packaging:

    200 drops in polymer cans. Banks are capped with screw caps.

    Each polymer can, along with instructions for medical use, is placed in a pack of cardboard or 32 cans of polymer, together with the corresponding number of instructions for medical use, are placed in a shrink film.

    Storage conditions:

    In the dark place at a temperature of no higher than 25 ° C.

    Keep out of the reach of children.

    Shelf life:

    1 year 6 months.

    Do not use after the date shown on the package.

    Terms of leave from pharmacies:Without recipe
    Registration number:LS-002472
    Date of registration:21.06.2010
    Expiration Date:Unlimited
    The owner of the registration certificate:PHARMSTANDART-UFIM VITAMIN FACTORY, OJSC PHARMSTANDART-UFIM VITAMIN FACTORY, OJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp26.09.2017
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