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SYNVISC is a sterile viscoelastic gel based on hylan G-F 20, designed for intra-articular injections. It temporarily restores the viscoelasticity of synovial fluid, relieves pain and improves mobility in joints affected by arthrosis or cartilage deficiency.
USE MEDICAL STRICT. Medical device. Injection of hyaluronic acid. Use reserved for dermatologists and aesthetic doctors because they require a medical procedure.
SYNVISC is a sterile gel:
- Viscoelastic based on hylan G-F 20, a sodium hyaluronate derivative, for intra-articular injection.
- Clear, slightly yellow, viscous and transparent, with no visible particles.
- It relieves pain and improves mobility in joints.
- SANOFI
- NAME: SYNVISC
- COMPOSITION: Sodium salt of hyaluronic acid, N-acetylglucosamine, sodium glucuronate, hylan G-F 20, hylan A, hylan B, saline, sodium chloride.
- PRESENTATION: 3 x 2 ml.
- NEEDLE: Use 18-22 G needles for SYNVISC.
- INDICATIONS: Temporarily restores the viscoelasticity of synovial fluid. Provides clinical benefit to patients in all stages of joint arthrosis.
- INJECTION DEPTH: Intra-articular injections within the synovial cavity of the joint.
- DURATION: 6 to 12 months.
- USE: Strict medical use.
- Syringes: 3 x 2 ml.
- Each box contains three pre-filled disposable glass syringes of SYNVISC.
SYNVISC TREATMENT ZONES
Ideal for arthrosis, cartilage deficiency and weak joints (knee, hip, shoulder, ankle).
Sodium salt of hyaluronic acid, N-acetylglucosamine, sodium glucuronate, hylan G-F 20, hylan A, hylan B, saline, sodium chloride.
- The efficacy of a course of treatment consisting of less than three injections (2 mL each) of SYNVISC has not been established.
- The safety and efficacy of SYNVISC at sites other than the knee and for diseases other than osteoarthritis have not been established.
- The safety and efficacy of using SYNVISC concomitantly with other intra-articular injectables have not been established.
- Use caution when injecting SYNVISC in patients allergic to proteins of avian origin, feathers or egg products.
- The safety and efficacy of SYNVISC in knee joints with severe inflammation have not been established.
- Strict adherence to an aseptic administration technique is required.
- Sterile content. The syringe is intended for single use only. The contents must be used immediately after opening the package. Discard any unused quantities of SYNVISC.
- Do not use SYNVISC if the packaging has been opened or damaged. Store in the original packaging (protected from light) at room temperature below 30 °C. DO NOT FREEZE.
- Remove any synovial fluid or effusion before each injection of SYNVISC.
- SYNVISC should be used with caution in patients with signs of lymphatic or venous stasis in the limb to be treated.
- Do not administer to patients with known hypersensitivity (allergy) to hyaluronan (sodium hyaluronate) preparations.
- Do not inject SYNVISC into the knees of patients with knee joint infections or skin diseases/infections in the area of the injection site.
SYNVISC is to be used in cases of topical difficulties of the locomotor system, particularly the osteo-articular system. It is indicated for arthralgia, joint stiffness, joint effusion, joint swelling, arthritis, arthropathy, gait disturbance.
SYNVISC serves to temporarily restore the viscoelasticity of synovial fluid, reducing joint pain and stiffness and improving mobility in joints affected by arthrosis.
Clinical benefits can last from 6 to 12 months, depending on the joint treated and the patient's activity.
A standard cycle involves three injections of 2 mL each; shorter cycles may not guarantee the same effectiveness.
Currently, efficacy is mainly established for the knee; use in other joints or for conditions other than arthrosis has not been fully evaluated.
It is essential to observe aseptic technique, to use the disposable syringe immediately and to remove any spillage or synovial fluid before injection; treatment should only be performed by qualified medical personnel.