BM Hyal-R Injection (Pre-filled) (Sodium Hyaluronate)
Sodium Hyaluronate 10mg
Prescription medication
BM Eye Co., Ltd.
MFDS item code 201402900 · Notified 2014.06.30 · Insurance code 654802201
Improvement of knee osteoarthritis and shoulder periarthritis
This medication is used to treat knee osteoarthritis and shoulder periarthritis.
Typically, for adults, one tube should be administered into the knee joint or shoulder joint (shoulder joint cavity, subacromial bursa, or biceps tendon sheath) once a week for three consecutive weeks; however, the number of administrations may be adjusted according to symptoms. This medication must be administered aseptically into the joint.
This medicine should not be used in patients who have had an allergic reaction to its ingredients. Caution should be taken for patients who have had allergic reactions to other medications, who have liver function issues, or who have skin diseases or infections at the injection site. Severe allergic reactions, such as shock, may occur during use, so the patient's condition should be closely monitored during administration. If symptoms of allergy such as swelling of the face or around the eyes, rash, or itching occur, use should be stopped immediately, and appropriate treatment should be sought. Temporary pain, swelling, redness, warmth, or severe pressure may occur at the injection site, and symptoms such as nausea, vomiting, and fever may also appear. If used in joints with severe inflammation, symptoms may worsen, so it is advisable to administer after inflammation has subsided. After administration, it is necessary to stabilize the affected area and ensure that the medication does not leak outside the joint. Aseptic conditions must be maintained during injection, and it is preferable not to repeat administration more than three times. If there is fluid accumulation in the joint, it is advisable to remove it before injection. Intravenous administration or use in the eyes is prohibited. Pregnant women or women of childbearing potential should carefully consider the benefits and risks of using this medication, and nursing mothers should avoid its administration. Safety has not been established in children, so it should only be used cautiously when necessary. Elderly patients may have reduced physical function, so special caution should be exercised.
Shock symptoms (severe allergic reaction)
Edema due to hypersensitivity (facial, eyelid, etc.), facial flushing, rash, urticaria, itching, pain, swelling, redness, warmth, local severe pressure, nausea, vomiting, fever
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a sealed container to prevent contact with air, and the storage temperature must be maintained between 1 and 30 degrees Celsius. Storing it this way will help maintain the efficacy of the medication and prevent deterioration.
A colorless, transparent, and viscous liquid contained in a glass or plastic tube (pre-filled syringe) sealed with rubber stoppers at both ends.
2.0mL/tube X 3
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.