HyalS Injection (Sodium Hyaluronate)
Sodium Hyaluronate 10mg
Prescription medication
HanKook Pavis Pharmaceutical Co., Ltd.
MFDS item code 201901577 · Notified 2019.03.14
This product's status changed to Expired on 2024.03.14. It may no longer be sold, so consult a doctor or pharmacist before taking it.
Relief of symptoms of knee osteoarthritis and shoulder periarthritis
This medication is primarily used for the treatment of knee osteoarthritis and shoulder periarthritis. Knee osteoarthritis is a disease resulting from damage to the cartilage of the knee joint, while shoulder periarthritis is inflammation of the tissues around the shoulder joint. This medication alleviates pain and inflammation associated with these joint diseases, reducing discomfort in daily life. It helps improve joint function, assisting patients to move more comfortably. Therefore, it is used in the treatment of knee osteoarthritis and shoulder periarthritis.
Typically, for adults, administer 1 vial once a week for 3 consecutive weeks into the knee joint cavity or shoulder joint (shoulder joint cavity, subacromial bursa, or biceps brachii tendon sheath), adjusting the frequency of administration as appropriate based on symptoms.
This medication is injected into the joint cavity as it contains sodium hyaluronate. First, it should not be used in patients who have previously experienced an allergic reaction to this medication. Additionally, it must be administered with caution in patients allergic to other medications or those with liver function issues or a history of liver disease. Care should also be taken if there are skin diseases or infections at the injection site. Serious allergic reactions such as shock may occur when using this medication, so administration should be stopped immediately if symptoms appear, and appropriate treatment should be received. Other allergic symptoms such as swelling of the face or around the eyes, rashes, hives, and itching may also occur, so caution is advised. Temporary pain, swelling, warmth, and tenderness may occur at the injection site, along with symptoms such as nausea, vomiting, and fever. If administered to an inflamed joint, symptoms may worsen, so it is advisable to reduce the inflammation first before use. After administration, stabilize the injection site and ensure the medication does not leak out of the joint cavity. Injections should be performed under sterile conditions, and if symptoms do not improve, administration should be limited to three times and then stopped. If there is liquid accumulation in the joint, it should be removed prior to injection. This medication is not suitable for intravenous injection or for use in the eyes. Women who are pregnant or may become pregnant should carefully consider the therapeutic effects and risks before using this medication, and nursing mothers are advised to avoid administration. Safety has not been established for children, so it should only be administered with caution when necessary. Elderly patients may have decreased physical function, requiring more careful use.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a sealed container to prevent exposure to air or moisture. It is important to maintain a storage temperature between 1 to 30 degrees Celsius to preserve the efficacy and safety of the medication.
A colorless, transparent, and viscous liquid contained in a glass vial sealed with rubber stoppers (part of a prefilled syringe system)
2ml x 1 vial, 2ml x 3 vials
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.