Active substanceCaffeine + Paracetamol + ChlorphenamineCaffeine + Paracetamol + Chlorphenamine
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  • Flucolidex®-H
    pills inwards 
  • Dosage form: & nbspPills
    Composition:

    Each tablet contains:

    Active substances: paracetamol -500.0 mg, caffeine anhydrous-30.0 mg, chlorphenamine maleate (chlorpheniramine maleate) 2.0 mg

    Excipients: gelatin-10.0 mg, corn starch-58.0 mg, talc-purified -5.0 mg, magnesium stearate-5.0 mg, carboxymethyl sodium starch-10.0 mg, povidone 30 (polyvinylpyrrolidone 30) 5.0 mg.

    Description:

    Round biconvex tablets white or almost white.

    Pharmacotherapeutic group:ARI and "colds" of symptoms remedy (analgesic non-narcotic remedy + psychostimulant + antihistamine)
    ATX: & nbsp

    N.02.B.E.71   Paracetamol in combination with psycholeptics

    Pharmacodynamics:

    Combined drug. Caffeine has a stimulating effect on the central nervous system, which leads to a reduction in fatigue and drowsiness, to an increase in mental and physical performance. Due to a combination of central and peripheral effects, the following effects: coronary vessels tend to expand, and the vessels of the brain - tonic, blood pressure slightly increases (more often with initial hypotension). Paracetamol renders antipyretic and analgesic action: reduces pain syndrome, observed in catarrhal conditions - sore throat, headache, muscle and joint pain, reduces heat.

    Chlorphenamine - a blocker of H1 - histamine receptors. It has an antiallergic effect: it removes the itch of the eyes, nose and throat, puffiness and hyperemia of the mucous membranes of the nasal cavity, nasopharynx and paranasal sinuses, reduces exudative manifestations.

    Pharmacokinetics:
    Indications:

    Symptomatic treatment of "cold" diseases, flu, ARVI (febrile syndrome, pain syndrome, rhinorrhea).

    Contraindications:

    Contraindications

    Hypersensitivity to paracetamol and other components that make up the drug; taking other drugs containing substances that are part of the drug; expressed violations of the liver or kidneys, children under 12 years.

    Carefully:

    With caution - pronounced arteriosclerosis of the coronary arteries, arterial hypertension, blood system diseases, deficiency of glucose-6-phosphate dehydrogenase, congenital hyperbilirubinemia (Gilbert syndrome, Dubin-Johnson and Rotor syndrome), alcoholism, angle-closure glaucoma,hyperplasia of the prostate, pregnancy, lactation.

    Pregnancy and lactation:with otoroĹžnostyu.
    Dosing and Administration:

    Apply usually 1 tablet 2-3 times a day at intervals of not less than 4 hours. The maximum single dose for adults and children over 12 years is 2 tablets, daily - 8 tablets. Duration of reception no more than 5 days. An increase in the duration of treatment is possible only under the supervision of a physician.

    Side effects:

    In therapeutic doses, the drug is usually well tolerated. Sometimes there are allergic reactions (skin rash, itching, hives, angioedema). Dizziness, nausea, excitation, insomnia, tachycardia, arrhythmia, epigastric pain, mydriasis, paresis of accommodation, increased intraocular pressure, dry mucous membranes, mouth, nose, throat; retention of urine. With prolonged use of large doses - hepatotoxic action, hemolytic or aplastic anemia, methemoglobinemia, thrombocytopenia, agranulocytosis, pancytopenia; nephrotoxicity (renal colic, glucosuria, interstitial nephritis, papillary necrosis).

    Overdose:

    Signs of acute poisoning caused by paracetamol - pallor of the skin, decreased appetite, nausea, vomiting, stomach pain, signs of liver damage are determined in 1-2 days. In severe cases, hepatonecrosis develops (the severity of necrosis, due to intoxication directly depends on the degree of overdose), hepatic insufficiency, encephalopathy and coma. Toxic effect in adults is possible after taking more than 10-15 g of paracetamol: increasing the activity of "liver" transaminases, increasing prothrombin time (12-48 hours after administration); a detailed clinical picture of liver damage manifests itself after 1-6 days. Rarely, liver failure develops at a lightning speed and can be complicated by renal insufficiency (tubular necrosis). The effect of caffeine can be manifested by periods of psychomotor agitation, tachycardia, cardiac arrhythmias, elevated diuresis, muscle cramps. Chlorpheniramine may be associated with dizziness, dry mouth, nausea, depression of the central nervous system.

    The victim, who took in a short time more than 15 tablets of the drug,should be done rinsing the stomach during the first 4 hours of poisoning, assign adsorbents, introduce agents that increase the formation of glutathione (methionine - 8-9 hours after an overdose, acetylcysteine - in the first 12 hours). Detoxification can be done by hemodialysis. Along with these measures, symptomatic therapy should be provided.

    Interaction:

    Nonsteroidal anti-inflammatory drugs, non-narcotic analgesics, and agents that depress the central nervous system can increase the side effect of the drug.

    The risk of developing a hepatotoxic effect increases with the simultaneous administration of barbiturates, phenytoin, carbamazepine, rifampicin, zidovudine and other inducers of microsomal liver enzymes, while consuming alcohol. With simultaneous use with levomitsetinom (chloramphenicol) excretion of the latter slows down and toxicity increases. The rate of absorption of paracetamol increases with metoclopramide or domperidone, the slowing of absorption occurs when combined with colestyramine.

    Long-term use of Flukoldeks®-H tablets with anticoagulants of indirect action should be performed under constant medical supervision.

    With prolonged (more than a week) application of the drug, control of the picture of peripheral blood and the functional state of the liver is necessary.

    Special instructions:

    Against the background of the use of Flukoldeks®-H tablets, other non-narcotic analgesics or non-steroidal anti-inflammatory drugs, as well as agents that depress the central nervous system, should not be taken. Avoid excessive consumption of tea, coffee and other products containing methylxanthines.

    To avoid the hepatotoxic effect of paracetamol, alcohol should not be used against the background of Flukoldeks®-H tablets.

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

    Because of the possible sedative effect of chlorphenamine is not recommended when using the drug to perform work that requires increased attention (driving vehicles, management mechanisms, etc.).

    Form release / dosage:

    For 4 tablets in a strip of aluminum foil or 12 tablets in a blister of aluminum foil and PVC.

    By 3, 50 strips or 1 blister in a pack of cardboard along with instructions for use.

    Storage conditions:

    In a dark place at a temperature of no higher than 30 ° C. Keep out of the reach of children.

    Shelf life:4 years.Do not use after expiry date.
    Terms of leave from pharmacies:Without recipe
    Registration number:P N 013278/01
    Date of registration:29.12.2011
    The owner of the registration certificate:Outline Pharma Pvt. Ltd.Outline Pharma Pvt. Ltd. India
    Manufacturer: & nbsp
    Representation: & nbspNPK Katren AONPK Katren AORussia
    Information update date: & nbsp29.12.2011
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