CHONDROITIN® INJECTION

  • Composition
  • Release form
  • Indication
  • Reception scheme
  • Contraindications
Active ingredient: chondroitin sulphate sodium; 1 ampoule (2 ml) contains chondroitin sodium sulfate in terms of 100% substance 200 mg; excipients: benzyl alcohol, water for injection.
2 ml ampoules. 10 ampoules in a pack or 5 ampoules in a blister, 2 blisters in a pack.
Degenerative-dystrophic diseases of the joints and spine: osteoarthritis, periarthritis of the shoulder scapula, osteochondrosis of the spine, fractures (to accelerate the formation of callus).
The drug should be administered to adults intramuscularly, 1 ml every other day. In case of good tolerance, increase the dose to 2 ml, starting with the fourth injection. The course of treatment is 25-35 injections. Repeated courses - after 6 months.
Hypersensitivity to any of the components of the drug, a tendency to bleeding, thrombophlebitis, renal failure, liver failure in the stage of decompensation, pregnancy, lactation.
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