Glucosamine (Glucosamine)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Active substanceGlucosamineGlucosamine
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    • Dosage form: & nbspPowder for solution for oral administration
    Composition:

    One package contains

    Active substance: glucosamine sodium sulfate chloride 1.884 g (equivalent to glucosamine sulfate - 1.5 g)

    Excipients: aspartame, sorbitol, macrogol-4000 (polyethylene glycol-4000), acid citric monohydrate until the mass of the contents of one packet is 3.95 g.

    Description:

    White or white with a slightly creamy tinge granular powder.

    Pharmacotherapeutic group:Reparation of tissue stimulant
    ATX: & nbsp

    M.01.A.X.05   Glucosamine

    Pharmacodynamics:

    Anti-inflammatory drug, replenishes the endogenous deficiency of glucosamine, increases the permeability of the joint capsule,restores enzymatic processes in the cells of the synovial membrane and articular cartilage. It promotes the fixation of sulfur during the synthesis of chondroitinsulfuric acid, facilitates the normal deposition of calcium in the bone tissue, inhibits the development of degenerative processes in the joints, restores their function, reducing joint pain.

    Pharmacokinetics:

    Quickly and completely absorbed in the small intestine. Bioavailability of 26%, half-life of 70 hours.

    Indications:

    Osteoarthrosis of peripheral joints, spine joints, osteochondrosis.

    Contraindications:

    Individual hypersensitivity to glucosamine and other components of the drug. Severe chronic renal failure, phenylketonuria, pregnancy, lactation, children under 12 years.

    Carefully:Bronchial asthma, diabetes mellitus. With intolerance to seafood (shrimp, shellfish), the likelihood of allergic reactions to the drug increases.
    Dosing and Administration:

    Adults and children from 12 years.

    Inside. The contents of one packet are dissolved in 200 ml of water, taken once a day for 6-12 weeks. On the appointment of a doctor, the course of treatment can be repeated at intervals 2 month.

    Side effects:

    From the digestive system: gastralgia, flatulence, constipation or diarrhea.

    Allergic reactions - Urticaria, itching.

    Overdose:

    Cases of overdose are unknown. Treatment: gastric lavage, symptomatic therapy.

    Interaction:

    Compatible with non-steroidal anti-inflammatory drugs, paracetamol and glucocorticosteroids.

    Increases the absorption of tetracyclines, reduces - semisynthetic penicillins, chloramphenicol.

    Form release / dosage:

    Powder for solution for oral administration 1.5 g.

    Packaging:

    By 3.95 g in heat-sealing bags of film combined multilayer material.

    By 5, 10, 20 or 30 bags with instructions for use in a pack of cardboard.

    Storage conditions:

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

    Keep out of the reach of children.

    Shelf life:

    3 years.

    Do not use after expiry date.

    Terms of leave from pharmacies:On prescription
    Registration number:LSR-009268/09
    Date of registration:17.11.2009 / 08.02.2016
    Expiration Date:Unlimited
    The owner of the registration certificate:FARMAKOR PRODUCTION, LTD. FARMAKOR PRODUCTION, LTD. Russia
    Manufacturer: & nbsp
    Information update date: & nbsp22.04.2017
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