Hilroad Plus Injection (Sodium Hyaluronate)
Sodium Hyaluronate 10mg
Injections · Prescription medication
Green Cross Wellbeing Co., Ltd.
MFDS item code 202401971 · Approved 2024.08.13 · Insurance code 681100541
Improvement of knee osteoarthritis and periarthritis of the shoulder
This medication is used to treat joint diseases such as knee osteoarthritis and periarthritis of the shoulder. It alleviates pain and inflammation in the joints, helping patients to lead a more comfortable daily life. It improves the range of motion in the joints and prevents functional deterioration. Thus, it is effective in restoring joint health and alleviating symptoms. Therefore, it is used for the treatment of knee osteoarthritis and periarthritis of the shoulder.
Typically, 1 injection per week for adults, with 1 syringe administered continuously over 3 weeks into the knee joint or shoulder joint (shoulder joint cavity, subacromial bursa, or biceps tendon), but the frequency may be adjusted according to symptoms.
This medication should not be used in patients with known allergies to its components. It should be used with caution in patients who have had allergies to other medications or have liver function issues or a history of liver disease. Additionally, care should be taken when administering this medication in areas with skin diseases or infections. Severe allergic reactions may occur when using this medication, so if symptoms develop, administration should be immediately discontinued and appropriate treatment should be sought. Transient pain, swelling, redness, and warmth may occur at the injection site, and rare symptoms such as nausea, vomiting, and fever may also appear. If there is severe inflammation in the joint, it is advisable to settle the inflammation first before using this medication. After administration, stabilizing the injection site can be helpful, and care must be taken to prevent the medication from leaking outside the joint. Injections must be performed in a sterile condition, and if there is no effect, administration should be stopped after three doses. If there is fluid pooling in the joint, it is advisable to drain the fluid if necessary before administration. This medication must not be administered intravenously or directly into the eyes, and appropriate needles should be used. Women who are pregnant or may become pregnant should use this medication cautiously only when the benefits outweigh the risks, and it is advisable to avoid use during breastfeeding. Safety has not been established in children, so it should only be used cautiously when absolutely necessary. Older patients may have decreased bodily function, so special caution should be exercised.
Shock symptoms (frequency unknown)
Swelling (facial, eyelid, etc.), facial flushing, rash, itching, pain (mainly transient pain after administration), swelling, edema, redness, warmth, severe localized pressure sensation, 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 air or moisture from entering. It is best to maintain storage temperatures between 1 degree and 30 degrees Celsius at room temperature.
An injection product in a colorless, transparent, viscous liquid filled in a colorless, transparent glass tube sealed at both ends with rubber stoppers (part of the prefilled syringe system)
2 milliliters/prefilled syringe [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.