Active substanceParacetamol + Chlorfenamine + Ascorbic acidParacetamol + Chlorfenamine + Ascorbic acid
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  • Dosage form: & nbsptablets effervescent with a taste of grapefruit, with a taste of raspberry
    Composition:

    For one tablet:

    Active substances:

    paracetamol - 500.00 mg

    chlorphenamine maleate - 10.00 mg

    ascorbic acid - 200.00 mg

    Excipients:

    With the taste of raspberries: sodium hydrogen carbonate, citric acid, sorbitol, povidone, sodium saccharinate, aspartame, sodium carbonate, macrogol, sodium lauryl sulfate, riboflavin-5-phosphate sodium, raspberry aroma (aromatic fruit additive "Malina"), flavor enhancer, red beet juice powder.

    With the taste of grapefruit: sodium bicarbonate, citric acid, sorbitol, povidone, aspartame, sodium carbonate, macrogol, sodium lauryl sulfate, lemon flavor (aromatic fruit additive "Lemon"), grapefruit flavor (aromatic fruit additive "Grapefruit"), flavor enhancer.

    Description:

    Tablets are effervescent with a taste of raspberries: Tablets are round, flat, with a bevelled edge and a dividing risk on one side, pink, pinkish-lilac or lilac, with lighter and darker patches, with a specific fruity odor.

    Tablets effervescent with a taste of grapefruit: The tablets are round, flat, with a bevelled edge and a dividing risk on one side, white, almost white or creamy white, with a barely noticeable marbling, with a specific citrus smell.

    Pharmacotherapeutic group:ARI and "colds" of symptoms remedy (analgesic non-narcotic means + H1-histamine receptor blocker + vitamin)
    ATX: & nbsp

    N.02.B.E.51   Paracetamol in combination with other drugs, excluding psycholeptics

    Pharmacodynamics:

    Combined drug.

    Paracetamol has analgesic and antipyretic effect; eliminates headache and other types of pain, reduces fever.

    Ascorbic acid (vitamin C) participates in the regulation of oxidation-reduction processes, carbohydrate metabolism, increases the body's resistance.

    Chlorphenamine - blocker of the Ngrostamine receptors, has an anti-allergic effect, facilitates breathing through the nose, reduces the feeling of nasal congestion, sneezing, lacrimation, itching and redness of the eyes.

    Indications:

    Infectious and inflammatory diseases (acute respiratory infections, influenza), accompanied by fever, chills, headache, joint and muscle pain, nasal congestion and pain in the throat and sinuses of the nose.

    Contraindications:

    - Hypersensitivity to paracetamol, ascorbic acid, chlorphenamine or any other component of the drug.

    - Erosive-ulcerative lesions of the gastrointestinal tract (in the phase of exacerbation).

    - Pronounced renal and / or hepatic insufficiency.

    - Alcoholism.

    - Closed-angle glaucoma.

    - Phenylketonuria.

    - Hyperplasia of the prostate.

    - Children's age (up to 15 years).

    - Pregnancy (I and III trimester) and lactation.

    Carefully:

    Pacute and / or hepatic insufficiency, deficiency of glucose-6-phosphate dehydrogenase, congenital hyperbilirubinemia (Gilbert syndrome, Dubin-Johnson and Rotor syndrome), hyperoxalaturia, progressive malignant diseases, viral hepatitis, alcoholic hepatitis, elderly age.

    Dosing and Administration:

    Inside. Adults and children over 15 years of age take 1 tablet 2-3 times a day. The tablet should be completely dissolved in a glass (200 ml) of warm water (50-60 ° C) and the resulting solution immediately drunk. It is better to take the drug between meals. The maximum daily dose is 3 tablets. The interval between doses should be at least 4 hours.

    In patients with impaired liver or kidney function and in elderly patients, the interval between doses should be at least 8 hours.

    Duration of admission without consulting a doctor is no more than 5 days when prescribed as an anesthetic and 3 days as an antipyretic.

    Side effects:

    The drug is well tolerated at recommended doses.

    In single cases there are:

    from the side of the central nervous system: headache, fatigue;

    from the digestive tract: nausea, pain in the epigastric region;

    from the endocrine system: hypoglycemia (up to the development of coma);

    from the hematopoiesis: anemia, hemolytic anemia (especially for patients with deficiency of glucose-6-phosphate dehydrogenase); extremely rare - thrombocytopenia;

    allergic reactions: skin rash, itching, urticaria, Quincke's edema, anaphylactoid reactions (including anaphylactic shock), multiform exudative erythema (including Stevens-Johnson syndrome), toxic epidermal necrolysis (Lyell's syndrome);

    Other: hypervitaminosis, metabolic disorders, fever, dry mouth, paresis of accommodation, urinary retention, drowsiness.

    All side effects of the drug should be reported to the doctor.

    Overdose:

    Symptoms of an overdose of the drug are due to the substances in its composition. The clinical picture of acute paracetamol overdose develops within 6-14 hours after its administration. Symptoms of chronic overdose appear after 2-4 days after increasing the dose of the drug. Symptoms of acute paracetamol overdose: diarrhea, decreased appetite, nausea and vomiting, abdominal discomfort and / or abdominal pain, increased sweating.

    Symptoms of an overdose of chlorphenamine: dizziness, agitation, sleep disorders, depression, convulsions.

    Treatment: symptomatic.

    Interaction:

    Increases the concentration in the blood of benzylpenicillin and tetracyclines.Improves absorption in the intestines of iron preparations (converts trivalent iron into bivalent); can increase the excretion of iron with simultaneous use with deferoxamine.

    Increases the risk of developing crystalluria in the treatment of salicylates and sulfonamides short-acting, slows the excretion of the 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.

    Ethanol enhances the sedative effect of antihistamines. Antidepressants, antiparkinsonics, antipsychotics (phenothiazine derivatives) - increase the risk of developing side effects (urine retention, dry mouth, constipation). Glucocorticosteroids - increase the risk of developing glaucoma.

    With simultaneous use reduces the chronotropic effect of isoprenaline.

    Can both increase and decrease the effect of anticoagulant drugs.

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

    Inductors of microsomal oxidation in the liver (phenytoin, ethanol, barbiturates, rifampicin, phenylbutazone, tricyclic antidepressants) increase the production of hydroxylated active metabolites, which makes it possible to develop severe intoxication with small overdoses. Ethanol promotes the development of acute pancreatitis.

    Inhibitors of microsomal oxidation (incl. cimetidine) reduce the risk of hepatotoxic effects. Simultaneous administration of the drug and diflunisala increases the concentration of paracetamol in the blood plasma by 50%, hepatotoxicity increases. Simultaneous reception of barbiturates reduces the effectiveness of paracetamol, increases the excretion of ascorbic acid in the urine.

    Paracetamol reduces the effectiveness of uricosuric drugs.

    Strengthens the effect of hypnotic drugs.

    Special instructions:

    When taking metoclopramide, domperidone, or colestyramine, it is also necessary to consult a doctor.

    With prolonged use in doses much higher than recommended, the probability of impaired liver and kidney function is increased, control of the peripheral blood picture is necessary.

    Paracetamol and ascorbic acid may distort the indicators of laboratory studies (quantitative determination of glucose and uric acid in the blood plasma, bilirubin, activity of "liver" transaminases, LDH).

    To avoid toxic damage to the liver paracetamol should not be combined with the reception of alcoholic beverages, but also to people prone to chronic alcohol consumption. The risk of liver damage increases in patients with alcoholic hepatosis.

    Assigning ascorbic acid to patients with rapidly proliferating and intensely metastatic tumors can aggravate the course of the process. In patients with elevated iron levels in the body, ascorbic acid should be used in minimal doses.
    Form release / dosage:Tablets are effervescent with raspberry taste, with a taste of grapefruit.
    Packaging:

    10 tablets in a plastic case; 1, 2, 4 or 6 tablets in a strip of Al / Al.

    1, 3, 5, 6, 10, 15, 20 strips in a cardboard bundle together with instructions for use.

    For 1 pencil case in a cardboard bundle or bundle-envelope with a device for hanging along with instructions for use.

    Storage conditions:

    At a temperature of 10-30 ° C.

    Keep out of the reach of children!

    Shelf life:

    3 years.Do not use after the expiration date.

    Terms of leave from pharmacies:Without recipe
    Registration number:LSR-005321/08
    Date of registration:07.07.2008 / 26.04.2017
    Expiration Date:Unlimited
    The owner of the registration certificate:VALEANT, LLC VALEANT, LLC Russia
    Manufacturer: & nbsp
    Representation: & nbspVALEANT LLC VALEANT LLC Russia
    Information update date: & nbsp06.09.2017
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