Румалон®

General characteristics. Structure:

Active ingredient: 2,5 mg of extract of cartilages and marrow of young animals in 1 ml of solution.

Excipients: метакризол, water for injections.

Pharmacological properties:

Pharmacodynamics. The drug Rumalon® contains a glikozaminoglikan-peptide complex from cartilages and marrow of young calfs. It exerts impact on the broken metabolism in cartilaginous hyaline tissue. Drug strengthens biosynthesis of the sulphated mucopolysaccharides. Stimulates regeneration of a joint cartilage and slows down catabolic processes in cartilaginous tissue.

Indications to use:

Degenerative changes of joints: gonartroza, arthroses of interdigital joints, coxarthroses, spondyloses, spondylarthroses, meniskopatiya, patella chondromalacia.

Route of administration and doses:

The drug is administered deeply intramusculary: in the first day - 0,3 ml, in the second day - 0,5 ml and further 3 times a week on 1 ml within 5-6 weeks. A repeated course of treatment – after consultation of the doctor according to the same scheme.

Side effects:

Allergic reactions (seldom).

Interaction with other medicines:

It is not revealed.

Contraindications:

The increased individual sensitivity, pseudorheumatism.

Storage conditions:

Period of validity - 5 years. Not to use after the period of validity specified on packaging. At a temperature from 18 to 20 °C in protected from light, the place, unavailable to children. Issue conditions from drugstores.

Issue conditions:

According to the recipe

Packaging:

Solution for intramuscular introduction. On 1 ml or 2 ml in ampoules of light-protective glass. On 5 ampoules in a blister strip packaging from a film polyvinyl chloride or in a blister strip packaging from a film of the polyvinyl chloride and printing aluminum foil varnished or a packing material. On 1, 2 blister strip packagings together with the application instruction and a knife ampoule or the scarificator in a pack from a cardboard. On 5 or 10 ampoules together with the application instruction and a knife ampoule or the scarificator in a pack with an insert with cells for ampoules in 1 or 2 rows from a cardboard. When using ampoules with a point or a ring of a break the knife ampoule or the scarificator is not put. On a pack in addition paste two protective labels (control of the first opening).