Rumalon (Rumalon for injections)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Active substanceGlycosaminoglycan-peptide complexGlycosaminoglycan-peptide complex
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  • Biartrin
    solution w / m 
    BINERGIYA, CJSC     Russia
  • Rumalon
    solution w / m 
    BRYNTSALOV-A, CJSC     Russia
    • Dosage form: & nbspsolution for intramuscular injection
    Description:

    Clear solution from pale-yellow with a brownish tint of color to yellowish brown with smell of metasrezole

    Pharmacotherapeutic group:Regeneration of the stimulant.
    ATX: & nbsp

    M.09.A.X   Other drugs for the treatment of diseases of the musculoskeletal system

    Pharmacodynamics:

    The drug Rumalon contains glycosaminoglycan-peptide complex from the cartilage and bone marrow of young calves. It affects the disturbed metabolism in the cartilaginous hyaline tissue. The drug enhances the biosynthesis of sulfated mucopolysaccharides. Stimulates the regeneration of articular cartilage and inhibits catabolic processes at cartilage tissue.

    Indications:

    Degenerative changes in joints: gonarthrosis, interdigital joint arthrosis, coxarthrosis, spondylosis, spondyloarthrosis, meniscopathy, patellar chondromalacia.

    Contraindications:

    Increased individual sensitivity, rheumatoid arthritis.

    Dosing and Administration:

    The drug is administered intramuscularly: on the first day - 0.3 ml, on the second day - 0.5 ml and then 3 times a week for 1 ml for 5-6 weeks.The repeated course of treatment is after consultation of the doctor according to the same scheme.

    Side effects:

    Allergic reactions (rarely).

    Interaction:

    Not found.

    Form release / dosage:

    Solution for intramuscular injection.


    Packaging:

    1 ml or 2 ml in the ampoules of the light-protective glass.

    By 5 ampoules in a contoured cell packaging made of a polyvinyl chloride film or in a contour cell box made of a polyvinylchloride film and aluminum foil printed lacquered or packaging material.

    For 1, 2 contour squares with instructions for use and a knife ampoule or scarifier in a pack of cardboard.

    For 5 or 10 ampoules together with the instructions for use and a knife ampoule or scarifier in a pack with an insert with cells for ampoules in 1 or 2 rows of cardboard.

    When using ampoules with a point or a fault ring, the ampoule knife or scarifier is not inserted.

    On the pack, two additional protective labels are attached (control of the first opening).

    Storage conditions:

    At a temperature of 18 to 20 ° C in a place out of the reach of children.

    Shelf life:

    5 years. Do not use after the expiration date printed on the package.

    Terms of leave from pharmacies:On prescription
    Registration number:P N001330 / 01-2002
    Date of registration:22.07.2008
    The owner of the registration certificate:BRYNTSALOV-A, CJSC BRYNTSALOV-A, CJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp20.01.2016
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