Clonax 2mL (Diclofenac β-Dimethylaminoethanol)
Diclofenac Beta-Dimethylaminoethanol 45mg
Injections · Prescription medication
Samchundang Pharmaceutical Co., Ltd.
MFDS item code 200100903 · Notified 2001.07.06 · Insurance code 651201781
Relief of inflammation and pain in rheumatoid arthritis and osteoarthritis (degenerative joint disease).
This medication is used for chronic joint diseases such as rheumatoid arthritis, osteoarthritis (degenerative joint disease), and ankylosing spondylitis. It also helps relieve inflammation and pain that occur after trauma and surgery. It is effective for alleviating pain associated with acute gout and pains around the kidneys and liver. It is used to improve inflammation and pain in various joints and soft tissues.
Administer 90mg of diclofenac beta-dimethylaminoethanol deeply into one side of the upper buttock daily. In severe cases, it may be administered twice daily at 90mg each, alternating injection into both sides of the buttocks. After the initial treatment period, it is recommended to switch to tablets or suppositories. Adjust doses according to age, disease, and symptoms. To minimize cardiovascular adverse reactions, the minimum effective dose should be used for the shortest duration.
People who regularly consume more than three glasses of alcohol a day should consult a doctor or pharmacist before taking this medication, as there is an increased risk of gastrointestinal bleeding when taking this medication or other antipyretic analgesics. Additionally, the ingredients in this medication may increase the risk of cardiovascular disease. Serious thrombotic reactions such as myocardial infarction or stroke may occur, so people with cardiovascular diseases or risk factors should be more cautious. This medication can cause severe gastrointestinal side effects such as gastrointestinal bleeding, ulcers, and perforation. The elderly or those with a history of gastrointestinal disease are at greater risk and should carefully monitor for gastrointestinal symptoms while taking this medication. Severe allergic reactions or chest pain may occur due to hypersensitivity, so if allergic symptoms appear, stop taking the medication immediately and consult a medical professional. Ampoule injections may have glass fragments when the container is cut, so caution should be exercised, especially for children or the elderly. Products containing benzyl alcohol may cause fatal respiratory problems in premature infants, so should not be administered to these patients. This medication should not be given to patients with peptic ulcers, severe blood disorders, liver or kidney disorders, severe hypertension, or heart failure. Patients with allergies to aspirin or other non-steroidal anti-inflammatory drugs or with a history of asthma should also not use this medication. Additionally, this medication should not be given to patients before and after coronary artery bypass graft surgery, or to newborns under 4 weeks, or to premature infants. Patients with specific diseases such as a history of peptic ulcer, liver or kidney disorders, hypertension, heart failure, or asthma should use this medication with caution, and special care is required for the elderly and children. Regular blood tests and liver and kidney function tests should be conducted while taking this medication, and any abnormal symptoms should be reported to a medical professional immediately, and the medication should be stopped. If symptoms such as headache, drowsiness, dizziness, skin rash, or difficulty breathing occur during use, the medication should be stopped immediately and a doctor should be consulted. During pregnancy, especially in the later stages, this medication may pose a risk to the fetus, so pregnant women should not use this medication and breastfeeding mothers should also stop breastfeeding or discontinue the medication as it may affect the baby. This medication may interact with other non-steroidal anti-inflammatory drugs, aspirin, lithium, warfarin, and so others, so patients taking other medications must consult a medical professional. Finally, this medication should be used at the minimum dose and for the shortest duration necessary, and patients should closely monitor for adverse reactions or changes in symptoms after taking it.
Chest tightness, difficulty breathing, hives, severe swelling (edema), shock, peptic ulcer, gastrointestinal bleeding, Stevens-Johnson syndrome, Lyell's syndrome, photosensitivity, jaundice, liver dysfunction, acute renal failure, oliguria, hematuria, asthma attacks, rashes, hives, severe allergic reactions, severe skin adverse reactions, severe edema or urinary abnormalities, Kounis syndrome (allergic vasospastic angina/allergic myocardial infarction), general malaise.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly sealed container that can block light, at a temperature between 1 degree and 30 degrees Celsius. This storage method helps maintain the medication's efficacy and safety.
A brown ampoule injection containing a colorless to pale yellow transparent liquid.
2mL X 50 ampoules
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.