Active substanceGlucosamineGlucosamine
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  • Dosage form: & nbspfilm coated tablets
    Composition:

    One film coated tablet shell contains

    Active active ingredient:

    Glucosamine sulfate potassium chloride in terms of glucosamine sulfate 750 mg

    Excipients: calcium carbonate - 455.00 mg, microcrystalline cellulose - 60,00 mg, stearic acid - 45,00 mg, silicon dioxide colloid - 22,50 mg, magnesium stearate - 15,00 mg, croscarmellose sodium - 15,00 mg.

    Sheath: hypromellose 20.00 mg, titanium dioxide 14.30 mg, triacetin 2.50 mg, propylene glycol 2.50 mg, dye sunset yellow (E110) 0.70 mg.

    Description:

    Biconvex oval tablets coated with a film coat from light yellow to dark yellow,with engraving "GS 750 "on one side of the tablet.

    Pharmacotherapeutic group:Reparation of tissue stimulant
    ATX: & nbsp

    M.01.A.X.05   Glucosamine

    Pharmacodynamics:

    Glucosamine helps to prevent cartilage destruction processes, stimulates the restoration of cartilaginous tissue, has anti-inflammatory and analgesic effect, normalizes the production of intra-articular fluid. Improves mobility of joints, reduces the need for non-steroidal anti-inflammatory drugs (NSAIDs).

    Indications:

    Osteoarthritis of peripheral joints and spine.

    Contraindications:

    Individual intolerance, marked violation of kidney function. Children under 18 years.

    Carefully:Bronchial asthma, diabetes, intolerance to seafood (shrimp, shellfish).
    Pregnancy and lactation:During pregnancy and breast-feeding, the drug is contraindicated.
    Dosing and Administration:

    Inside. Adults take 1 tablet 2 times a day.

    Steady therapeutic effect is achieved with taking the drug for 6 months.
    Side effects:

    Disturbances of the function of the gastrointestinal tract (epigastric pain, flatulence, diarrhea, constipation, nausea),skin allergic reactions (hives, itching of the skin).

    Overdose:

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

    Interaction:

    Increases the absorption of tetracyclines, reduces the effect of semisynthetic penicillins, chloramphenicol. The drug is compatible with paracetamol, NSAIDs and glucocorticosteroids. When combined with NSAIDs, it increases the anti-inflammatory and analgesic effect of the latter.

    Special instructions:

    It is not recommended for children under 18 years of age due to a lack of scientific data for this category of patients. The risk of allergic reactions increases with intolerance to seafood.

    Effect on the ability to drive transp. cf. and fur:No data.
    Form release / dosage:

    Film coated tablets 750 mg.

    Packaging:

    For 60 tablets in a polyethylene bottle with a screwed polyethylene lid and a safety valve made of foil. The label is attached to the vial, the bottle with the lid is tightened with a polyethylene film, and together with the instruction for use is placed in a cardboard box.

    For 15 tablets in a blister of aluminum foil / HBH; 4 or 8 blisters together with instructions for use are placed in a cardboard box.

    Storage conditions:

    In a dry place, at a temperature of 10-30 ° C.

    Keep out of the reach of children.

    Shelf life:5 years. Do not use after the expiration date.
    Terms of leave from pharmacies:Without recipe
    Registration number:П N015968 / 01
    Date of registration:15.07.2009
    Expiration Date:Unlimited
    The owner of the registration certificate:Unipharm, Inc.Unipharm, Inc. USA
    Manufacturer: & nbsp
    Representation: & nbspUNIFARM, Inc. UNIFARM, Inc. USA
    Information update date: & nbsp22.04.2017
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