Active substanceAscorbic acidAscorbic acid
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  • Dosage form: & nbspsolution for intravenous and intramuscular administration
    Composition:

    Composition per ml:

    active substance: ascorbic acid -50 mg or 100 mg;

    Excipients: Baking soda (sodium bicarbonate) -23.85 mg or 47.7 mg of sodium pirosernistokisly (sodium metabisulfite) - 2 mg Water for injection - up to 1 ml.

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

    A.11.G.A.01   Ascorbic acid

    Pharmacodynamics:

    Ascorbic acid (vitamin C) is not formed in the human body, but comes only with food.

    Pharmacological effects: in quantities significantly exceeding the daily requirement (90 mg), almost no effect, except for the rapid elimination of symptoms of hypo- and avitaminosis (scurvy).

    Physiological functions: is a cofactor of some reactions hydroxylation and amidation - transfers electrons to enzymes, providing them with a replacement equivalent. Participates in the reactions of hydroxylation of proline and lysine residues of procollagen with the formation of hydroxyproline and hydroxylizine (poststranslational modification of collagen), the oxidation of the side chains of lysine in proteins with the formation of hydroxytrimethyllysine (during the synthesis of the picture), the oxidation of folic acid to folinic, metabolism drug in liver microsomes and hydroxylation of dopamine with the formation of norepinephrine.

    Increases the activity of amidating enzymes involved in the processing of oxytocin,antidiuretic hormone (ADH) and holitsistokinina. Participates in steroidogenesis in the adrenal glands.

    The main role in the tissues is the participation in the synthesis of collagen, proteoglycans and other organic components of the intercellular substance of the teeth, bones and endothelium of the capillaries.

    The main role in the tissues is the participation in the synthesis of collagen, proteoglycans and other organic components of the intercellular substance of the teeth, bones and endothelium of the capillaries.

    Pharmacokinetics:

    Connection with plasma proteins - 25 %.

    The concentration of ascorbic acid in the plasma is normally around 10-20 μg / ml. Easily penetrates into leukocytes, platelets, and then into all tissues; the greatest concentration is achieved in glandular organs, leukocytes, liver and lens of the eye; penetrates the placenta. The concentration of ascorbic acid in leukocytes and platelets is higher than in erythrocytes and in plasma. With deficient states, the concentration in leukocytes decreases later and more slowly and is considered as the best criterion for assessing the deficit than the concentration in the plasma.

    Metabolised mainly in the liver in desoxyascorbic and then in oxaloacetic acid and ascorbate-2-sulfate.

    It is excreted by the kidneys, through the intestines, with sweat, breast milk in unchanged form and in the form of metabolites.

    At the appointment of high doses, the rate of excretion increases sharply. Smoking and the use of ethanol accelerate the destruction of ascorbic acid (conversion into inactive metabolites), sharply reducing the reserves in the body.

    It is in hemodialysis.

    Indications:

    Treatment of hypo-and avitaminosis C (if necessary, rapid replenishment of vitamin C and the impossibility of oral administration).

    Applied for medical purposes in all clinical situations associated with the need for additional administration of ascorbic acid, including: parenteral nutrition, diseases gastrointestinal tract (GIT): (Persistent diarrhea, resection of the small intestine, peptic ulcer, gastrectomy), Addison's disease.

    In laboratory practice: for the marking of erythrocytes (together with sodium chromate Cr51).

    Contraindications:

    Hypersensitivity, with prolonged use in large doses (more than 500 mg) - diabetes mellitus, hyperoxaluria, nephrolithiasis, hemochromatosis, thalassemia, deficiency of glucose-6-phosphate dehydrogenase.

    Carefully:Diabetes mellitus, deficiency of glucose-6-phosphate dehydrogenase, hemochromatosis, sideroblastic anemia, thalassemia, hyperoxaluria, kidney stone disease.
    Pregnancy and lactation:

    The use of the drug during pregnancy and lactation is possible only according to the prescription of the doctor in the event that the intended use for the mother exceeds the potential risk to the fetus or baby.

    Dosing and Administration:

    Intramuscularly, intravenously (slowly), adults from 100 to 500 mg (2-10 ml of 5% solution) per day, with scurvy therapy - up to 1000 mg per day.

    Children from 100 to 300 mg (2-6 ml of 5 % solution) per day, with scurvy therapy - up to 500 mg (10 ml of 5% solution) per day.

    For the marking of erythrocytes (together with sodium chromate Cr51) - 100 mg of ascorbic acid is injected into a bottle of sodium chromate Cr51.

    Side effects:

    From the central nervous system (CNS): with rapid intravenous injection - dizziness, fatigue, with prolonged use of large doses (more than 1 g) - headache, increased excitability of the central nervous system, insomnia.

    From the urinary system: moderate, pollakiuria (with application of a dose of more than 600 mg / day), with prolonged use of large doses - hyperoxaluria, nephrolithiasis (from calcium oxalate),damage to the glomerular apparatus of the kidneys.

    From the cardiovascular system (SSS): at long application of the big doses - depression of permeability of capillaries (probably deterioration of a trophism tissues, increased blood pressure, hypercoagulation, development microangiopathy).

    Allergic reactions: skin rash, skin hyperemia.

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

    Local reactions: pain in the place of intramuscular injection.

    Other: with prolonged use of large doses (more than 1 g) - suppression of the function of the insulin pancreas apparatus (hyperglycemia, glucosuria), with intravenous administration - the threat of abortion (due to hyperestrogenemia), hemolysis of erythrocytes.

    Overdose:

    Symptoms: nephrolithiasis, insomnia, irritability, hypoglycemia.

    Treatment: symptomatic, forced diuresis.

    Interaction:

    Increases the concentration in the blood of benzylpenicillin and tetracyclines; in a dose of 1 g / day increases the bioavailability of ethinyl estradiol (including those included in oral contraceptives).

    Reduces the effectiveness of heparin and indirect anticoagulants.

    With simultaneous use with acetylsalicylic acid (ASA), urinary excretion of ascorbic acid increases and the excretion of ASA decreases.

    Increases the risk of developing crystalluria in the treatment of salicylates and sulfonamides short-acting, slows the excretion of acids by the kidneys, increases the excretion of the drug with 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.

    The drugs of quinoline series, calcium chloride, salicylates, glucocorticosteroid preparations 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 interfere with the interaction of disulfiram and ethanol.

    In high doses increases the excretion of mexiletine by the kidneys.

    Barbiturates and primidon increase the excretion of ascorbic acid in the urine.Reduces the therapeutic effect of antipsychotic drugs (neuroleptics) - phenothiazine derivatives, tubular reabsorption of amphetamine and tricyclic antidepressants.

    Pharmaceutically incompatible with aminophylline, bleomycin, cefazolin, cefapyrin, chlordiazepoxide, estrogens, dextrans, doxapram, erythromycin, methicillin, nafcillin, benzylpenicillin, warfarin.

    Special instructions:

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

    High doses of ascorbic acid increase the excretion of oxalates, promoting the formation of kidney stones. In newborns, whose mothers took high doses of ascorbic acid, and in adults who took high doses, there may be a "ricochet" scurvy.

    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.

    Ascorbic acid as a reducing agent can distort the results of various laboratory tests (blood and urine content of glucose, bilirubin, activity of "liver" transaminases and lactate dehydrogenase (LDH)).

    Effect on the ability to drive transp. cf. and fur:During the treatment period, care must be taken when driving and potentially dangerous mechanisms due to possible dizziness, fatigue and increased blood pressure.
    Form release / dosage:Solution for intravenous and intramuscular injection 50 mg / ml and 100 mg / ml.
    Packaging:

    1 ml (for a concentration of 50 mg / ml), 2 ml (for a concentration of 50 mg / ml and 100 mg / ml) in neutral glass ampoules.

    For 10 ampoules together with a knife ampoule or scarifier and instructions for use are put in a pack of cardboard and paste a label-parcel post.

    It is allowed to put the text of the label-parcel directly on the packet.

    5 ampoules are placed in a contour mesh box made of polyvinyl chloride film and aluminum foil, or without foil.

    2 contour squares with a knife ampoule or scarifier and instructions for use are placed in a pack of cardboard and gluedsticker-parcel.

    It is allowed to put the text of the label-parcel directly on the packet.

    When packing ampoules with a break point or a fracture ring, the ampoule knife or scarifier is not inserted.

    Storage conditions:

    In the dark place at a temperature of no higher than 30 ° C.

    Keep out of the reach of children.

    Shelf life:

    1.5 years for the solution with a dosage of 50 mg / ml.

    1.5 years for the solution with a dosage of 100 mg / ml.

    Terms of leave from pharmacies:On prescription
    Registration number:LP-000026
    Date of registration:08.11.2010 / 12.04.2016
    Expiration Date:Unlimited
    The owner of the registration certificate:Armavir Biofactory, FKPArmavir Biofactory, FKP Russia
    Manufacturer: & nbsp
    Information update date: & nbsp26.09.2017
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