OSTENIL TENDON solution injectable (1x2ml)
Forms , Presentations
Viscoelastic solution for peritendinous injection or injection into the tendon synovial sheath :
Prefilled syringe 40 mg / 2 ml in sterile packaging , box unit . Sterilized by moist heat.
composition
Isotonic solution : p ml
Sodium hyaluronate *
20 mg
Excipients: sodium chloride, monosodium phosphate , disodium phosphate, mannitol , water for injections .
*
Originally fermentative .
properties
Solid structure made of fibrous connective tissue , tendon transmits the efforts of muscles to bones and resistance to tension during muscle contraction. Tendons can be surrounded by various structures , eg retinacula , synovial tendon sheaths , peritendon , bursae . Excessive stress or inappropriate biomechanical stress can cause inflammation and / or degenerative changes in tendons, causing pain and loss of function . Lubricate the tendon can reduce pain, improve function and tendon reduce the possibility of occurrence of adhesions. Due to its viscoelastic properties and lubricating , Ostenil tendon promotes slidability tendons and the physiological processes of regeneration . Furthermore , due to its macromolecular structure , reduced Ostenil Tendon free passage of cells and pro-inflammatory molecules by synovial tendon sheath .
Tendon Ostenil is a transparent solution containing sodium hyaluronate natural highly purified product by fermentation and thus containing no animal protein . Tendon Ostenil also contains mannitol , a free radical scavenger , which helps stabilize the chains of sodium hyaluronate . Biocompatibility studies have shown qu'Ostenil Tendon was particularly well tolerated.
use
Pain and mobility limitation in case of disorders of tendons.
Instructions
Injected around the tendon Tendon Ostenil reached or tendon synovial sheath reached once a week , for a total of two injections. Several tendons can be treated simultaneously. Repeat treatments are possible if necessary .
The content and the outer surface of the pre-filled syringe Ostenil Tendon remain sterile as sterile packaging remains intact.
Remove the pre-filled syringe of sterile packaging , remove the closing cap Luer -Lok ™ syringe , attach a suitable needle (eg 25 to 27 G) and ensure its proper mounting by turning slightly . Before injection , be sure to remove the syringe any air bubbles that may be present .
Cons -indications
Do not use Ostenil Tendon in patients with known hypersensitivity to any component .
Precautions
When using Ostenil Tendon, special attention should be paid to patients with known hypersensitivity to drugs.
General precautions related to peritendinous injections or injections into the tendon synovial sheath must be respected.
Ostenil Tendon must be injected correctly in tendon synovial sheath around the tendon or injured , if necessary under fluoroscopic control. Avoiding damage to the nerves and blood vessels in injections .
In the absence of clinical data on the use of hyaluronic acid in children, pregnant or lactating women , administration of Ostenil Tendon is not recommended in these patients acid.
Do not use if the prefilled syringe or sterile packaging is damaged. Any unused solution immediately after opening should be discarded if sterility can not be guaranteed .
interactions:
To date, no data are available on the incompatibility of Ostenil Tendon with other products used for the tendons.
Side effects:
After using Ostenil Tendon, concurrent local events such as pain , warmth , bruising, redness and swelling may occur.
Storage conditions
Store at a temperature between 2 ° C and 25 ° C.
Do not use after the expiry date stated on the carton .
Keep out of reach of children.
Réf. : 5173774003304