Product image of Hyalgan (Sodium Hyaluronate) supplied by GNH India

Hyalgan

Active Ingredient:
Sodium Hyaluronate
Origin:
EU

Hyalgan (Sodium Hyaluronate)

Hyalgan is a prescription intra‑articular injection containing sodium hyaluronate, a form of hyaluronic acid, supplied as a sterile solution for joint administration. The product is marketed in the European Union and classified as a viscosupplement. It is administered by a healthcare professional directly into the affected knee joint to help restore viscoelastic properties and support joint function. The treatment is intended for patients with symptomatic osteoarthritis.

Manufacturer / TM Owner

Fidia Farmaceutici S.P.A

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Indications & Clinical Uses

Hyalgan is indicated for the symptomatic treatment of osteoarthritis of the knee when other conservative measures have not provided adequate relief.

  • Management of knee osteoarthritis pain in adults.
  • Adjunct to physical therapy and exercise programs.
  • Use in patients who are unsuitable for oral NSAIDs.
  • May be considered when intra‑articular corticosteroids are contraindicated.
  • Intended for single‑joint administration, typically a series of weekly injections.

How It Works

  • Sodium hyaluronate in Hyalgan mimics the natural hyaluronic acid component of synovial fluid. After intra‑articular injection, the polymer integrates into the joint space, increasing the concentration of high‑molecular‑weight hyaluronate. This enhances the viscoelasticity of synovial fluid, improving lubrication and shock absorption. The restored fluid dynamics reduce mechanical stress on cartilage and may modulate inflammatory mediators, contributing to pain relief and functional improvement.

Side Effects

Adverse reactions to Hyalgan are generally related to the injection procedure and the product itself. Reported events range from mild, transient symptoms to rare serious complications.

Common

  • Mild pain or tenderness at the injection site lasting a few hours.
  • Local swelling or joint effusion that resolves within a few days.
  • Warmth or mild erythema around the injection area without systemic signs.
  • Temporary stiffness or reduced range of motion that improves with activity.
  • Transient headache or flu‑like symptoms such as low‑grade fever.

Serious

  • Acute septic arthritis requiring antibiotics or surgical drainage.
  • Allergic reaction ranging from urticaria or rash to anaphylactic shock.
  • Persistent severe synovitis with marked swelling and pain.
  • Joint hemorrhage (hemarthrosis), particularly in patients receiving anticoagulant therapy.
  • Nerve injury leading to prolonged numbness, tingling, or weakness in the leg.

Precautions & Warnings

Before using Hyalgan, clinicians should evaluate patient history and joint condition to minimize risks and ensure appropriate use.

  • Confirm diagnosis of knee osteoarthritis and consider alternative therapies first.
  • Avoid injection in infected or inflamed joints, or in the presence of active skin disease over the injection site.
  • Use caution in patients with a history of hypersensitivity to hyaluronic acid preparations.
  • Assess bleeding risk; postpone treatment in patients on anticoagulants or with coagulation disorders.
  • Monitor for signs of infection or severe inflammation after each injection.
  • Do not use in pregnant or nursing women unless benefits outweigh potential risks.

Avoid Interactions

Hyalgan may interact with other agents that affect joint health or bleeding risk, and certain medications can influence the safety of intra‑articular injections.

Avoid

  • Concurrent intra‑articular corticosteroids or other viscosupplements in the same joint.
  • Administration during an active joint infection or systemic infection.

Use with caution

  • Anticoagulant or antiplatelet therapy (e.g., warfarin, aspirin, clopidogrel) due to increased bleeding risk.
  • Systemic non‑steroidal anti‑inflammatory drugs (NSAIDs) that may mask signs of joint infection.
  • Disease‑modifying osteoarthritis drugs that could alter joint environment.
  • Immunosuppressive agents that may predispose to infection.

Frequently Asked Questions

Hyalgan is a sterile injection of sodium hyaluronate, a form of hyaluronic acid, designed to supplement the natural synovial fluid in the knee. Unlike corticosteroid injections, it aims to restore joint lubrication rather than reduce inflammation.

A healthcare professional injects Hyalgan directly into the affected knee joint, usually following aseptic technique. The treatment course often consists of a series of weekly injections, but the exact schedule is determined by the prescribing clinician.

Adults with symptomatic knee osteoarthritis who have not achieved sufficient relief from oral analgesics, physical therapy, or lifestyle modifications may be considered. Patients with active joint infection or known hypersensitivity to hyaluronic acid are not suitable.

A common regimen involves multiple injections (often five) administered once weekly into the same knee. The total number and frequency are individualized based on clinical response and physician judgment.

Patients may experience pain reduction and improved function for several months after completing the injection series, though individual duration of benefit varies.

Yes, Hyalgan is often combined with physical therapy, exercise, and weight‑management programs to maximize functional improvement and joint health.

Typical mild reactions include injection‑site pain, swelling, warmth, erythema, temporary stiffness, and occasional flu‑like symptoms such as low‑grade fever or headache.

Patients should seek medical attention for signs of infection (e.g., increasing pain, fever, redness), allergic reactions (rash, hives, difficulty breathing), joint bleeding, or persistent severe inflammation.

Contraindications include active joint infection, known allergy to hyaluronic acid products, and severe skin disease over the injection site. Caution is advised in pregnancy, nursing, and bleeding disorders.

The skin over the knee should be cleaned with an antiseptic solution, and the joint may be aspirated to remove excess fluid if needed. Patients should inform the clinician of any medications, especially blood thinners.

Patients on anticoagulant or antiplatelet therapy have an increased risk of joint bleeding. The clinician may adjust the medication regimen or monitor closely after injection.

After each injection, patients should monitor the knee for swelling, pain, or signs of infection and report concerns promptly. Follow‑up visits allow the clinician to assess response and plan subsequent injections if needed.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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