Medication info

Hyaluric Injection (Pre-filled) (Sodium Hyaluronate)

Prescription medicationInjectionsApproval withdrawn
Ingredient · strength
Sodium Hyaluronate›10mg / 1mL
Manufacturer / importer
(주)대웅제약
Appearance
A pre-filled injectable solution containing a colorless, transparent, viscous liquid inside a glass vial sealed with rubber stoppers at both ends (part of a pre-filled syringe system).
Packaging
2ml/vial x 3
Approval status
Approval withdrawn

MFDS item code 201905318 · Notified 2019.07.26

This product's status changed to Approval withdrawn on 2023.12.06. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Improvement of knee osteoarthritis and periarthritis of the shoulder.
Who uses it
Adults
Adult dosage
Typically administered to adults once a week, one vial for three consecutive weeks into the knee joint or shoulder joint (shoulder joint cavity, subacromial bursa, or bicipital tendon sheath), but the frequency of administration should be adjusted according to symptoms. This medication is administered intra-articularly, so it should be performed under strict aseptic conditions.

Ingredients

Manufacturer
(주)대웅제약

Efficacy & effects

Improvement of knee osteoarthritis and periarthritis of the shoulder.

  • Knee osteoarthritis
  • shoulder periarthritis.
View approved original text

This medication is primarily used for the treatment of knee osteoarthritis and shoulder periarthritis. Osteoarthritis is a condition where the cartilage of the joint is damaged, leading to pain and mobility issues, while shoulder periarthritis represents inflammation of the tissues around the shoulder joint causing pain and functional decline. This medication helps relieve inflammation and reduce pain, aiding in the recovery of joint function. It is, therefore, effective for alleviating pain and inflammation in knee and shoulder joints. It is used for the treatment of knee osteoarthritis and shoulder periarthritis.

Dosage and Administration

Adult dosage

Typically administered to adults once a week, one vial for three consecutive weeks into the knee joint or shoulder joint (shoulder joint cavity, subacromial bursa, or bicipital tendon sheath), but the frequency of administration should be adjusted according to symptoms. This medication is administered intra-articularly, so it should be performed under strict aseptic conditions.

Precautions

This medication should not be used in patients who have had allergic reactions to its components. It should also be used cautiously in patients who have had allergic reactions to other medications or have liver function issues or a history of liver disease. Care should be taken if there are skin diseases or infections in the joint area, as this medication is injected directly into the joint. When using this medication, it is crucial to monitor the patient closely, as severe side effects such as shock may occur. If any abnormal symptoms appear, discontinue use immediately and seek appropriate treatment. Additionally, allergy symptoms such as swelling of the face or around the eyes, rash, or itching may appear; if these symptoms occur, use should be stopped. Temporary pain, swelling, redness, warmth, and severe pressure can occur at the injection site. Sometimes symptoms like nausea, vomiting, and fever may also occur, so caution is advised. If the joint is severely inflamed, it is advisable to treat the inflammation first before using this medication. Stabilizing the injection site post-injection can be helpful. If this medication leaks outside the joint, it may cause pain, so it must be injected accurately into the joint. Strict aseptic technique must be maintained during injection, and if symptoms do not improve, administration should be limited to three doses and then discontinued. If there is excessive fluid in the joint, aspiration prior to injection may be necessary. This medication is not suitable for intravenous use or ocular application. Using an injection needle of size 22-23 gauge is recommended. Also, care should be taken as mixing with certain disinfectants may cause precipitation of the drug. Pregnant women or those who may become pregnant should carefully weigh the benefits and risks of using this medication, and it is best to avoid use during breastfeeding. For children, safety has not been established, so it should be used cautiously only when necessary. Elderly patients may have impaired bodily functions, thus requiring even more careful use.

Side effects and when to seek care immediately

Serious side effects

Shock symptoms (severe allergic reaction).

Mild side effects

  • Facial swelling
  • eyelid swelling
  • facial flushing
  • rash
  • hives
  • itching
  • transient pain
  • swelling
  • redness
  • warmth
Show 4 more
  • severe local pressure
  • nausea
  • vomiting
  • fever.

Not everyone experiences these, and they can vary from person to person.

Storage

This medication should be stored in a sealed container that prevents air ingress, ideally at room temperature between 1 and 30 degrees Celsius. This will help maintain the drug's efficacy and ensure safe usage.

Appearance and packaging

Appearance

A pre-filled injectable solution containing a colorless, transparent, viscous liquid inside a glass vial sealed with rubber stoppers at both ends (part of a pre-filled syringe system).

Package unit

2ml/vial x 3

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

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.

Questions about this medicine

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For anything that needs medical judgment, consult a doctor or pharmacist.

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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.