Sodium hyaluronate injection
Function and Efficacy
Sodium hyaluronate is the main component of synovial fluid and one of the components of cartilage matrix. It plays a lubricating role in the joint cavity, reducing friction between tissues, and at the same time plays an elastic role, buffering the effect of stress on articular cartilage, and exerting its due physiological function. Injecting high molecular weight, high concentration, and high viscoelastic sodium hyaluronate into the joint cavity can significantly improve the inflammatory response of synovial tissue, increase the sodium hyaluronate content in the synovial fluid, enhance the viscosity and lubrication function of the joint fluid, protect the articular cartilage, promote the healing and regeneration of articular cartilage, relieve pain, and increase joint mobility.
Ingredients
The main ingredient of this product is sodium hyaluronate.
| Name | Description | Content | CAS NO. | Manufacturer |
|---|---|---|---|---|
| Sodium hyaluronateIngredients |
Sodium hyaluronate is the main component of synovial fluid and one of the components of cartilage matrix. It plays a lubricating role in the joint cavity, reducing friction between tissues, and at the same time plays an elastic role, buffering the effect of stress on articular cartilage, and exerting its due physiological function. Injecting high molecular weight, high concentration, and high viscoelastic sodium hyaluronate into the joint cavity can significantly improve the inflammatory response of synovial tissue, increase the sodium hyaluronate content in the synovial fluid, enhance the viscosity and lubrication function of the joint fluid, protect the articular cartilage, promote the healing and regeneration of articular cartilage, relieve pain, and increase joint mobility. More |
9067-32-7 | 33 |
Appearance
This product is a colorless, clear, viscous liquid.
Indication
Knee osteoarthritis, frozen shoulder, etc.
Usage and Dosage
This product is a drug for improving knee osteoarthritis, frozen shoulder and other symptoms. When used for knee osteoarthritis, it is injected into the knee joint cavity; when used for frozen shoulder, it is injected into the shoulder joint cavity or subacromial bursa. 2mi each time, once a week, 5 weeks as a course of treatment
Adverse Reactions
Some patients may experience symptoms such as pain, rash, and itching at the injection site, which usually disappear on their own within 2-3 days. If the symptoms persist, the medication should be stopped and necessary treatment should be carried out.
Special Population Medication
Precautions for children: Not yet clear. Precautions for pregnancy and lactation: Not yet clear. Precautions for the elderly: Not yet clear.
Drug Interactions
Not yet clear.
Storage
Keep in a dark place and sealed at 2-8℃.
Packaging Specification
2 ml: 20 mg
Validity Period
Tentative two years
Manufacturer
Shandong Bausch & Lomb Freda Pharmaceutical Co., Ltd.
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Founded in:
1992-03-31 -
Address:
No. 789, Xinluo Street, Jinan High-tech Development Zone -
Tax NO.:
913701006140705563 -
Registered Funds:
90 million yuan -
Website:
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Email: