Durolane® 3ml 20mg/ml

Price range: $247.00 through $259.00

DUROLANE® is a clear, viscous gel that contains highly-purified sodium hyaluronate. Sodium hyaluronate is found in the body, particularly in joint tissue and fluid surrounding the joint. This substance acts as a lubricant and shock absorber in the knee joint.

In joints affected by osteoarthritis, the concentration of sodium hyaluronate and its ability to lubricate and cushion may be reduced. Therefore, injection of sodium hyaluronate directly into the joint may increase lubrication and cushioning, relieving pain during physical activity. The sodium hyaluronate in DUROLANE® is produced by bacterial fermentation.
DUROLANE® is provided to your doctor as a single syringe containing 3 ml of gel.

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Durolane® (3ml, 20mg/ml) is a single-injection, high-concentration hyaluronic acid treatment designed to relieve knee or hip osteoarthritis pain for up to 6–26 weeks. It acts as a lubricant and shock absorber, targeting patients who have not found relief through conservative therapies. It is a, non-animal-derived product.

 

Key Details of Durolane (3ml, 20mg/ml):
Purpose: Treats knee and hip osteoarthritis (OA) pain by restoring joint viscosity and elasticity.
Application: Single intra-articular injection, often providing longer-lasting relief than steroid injections.
Composition: 3ml sterile syringe containing 20mg/mL of stabilized sodium hyaluronate (NASHA®) in phosphate-buffered saline.
Side Effects: Potential minor, transient side effects include injection site pain, swelling, stiffness, or warmth.
Storage: Store between 2°C – 25°C.
Contraindications: Do not use if you have infections or severe skin diseases around the knee joint.

WHAT ARE THE POSSIBLE SIDE EFFECTS?

Common side effects (also called reactions) that may occur during the use of DUROLANE® include pain, joint pain, joint swelling, and joint stiffness at the injection site. The majority of reactions are mild to moderate in nature and do not last long. No treatmentrelated allergic reactions or acute-inflammatory reactions or hypersensitivity to DUROLANE® have been reported from the controlled clinical studies.

If any of the above symptoms or signs appear after you are given DUROLANE®, or if you are experiencing any other problems, you should call your healthcare professional.

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1-5, 6-10, 11-20, 21+

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