Ciox Capsule (Meloxicam)

Adult dose

Acute exacerbations of osteoarthritis (degenerative arthritis): Adults: Administer 7.5 mg of meloxicam orally once daily. If symptoms do not improve, the dose may be increased to 15 mg per day as needed. Rheumatoid arthritis, ankylosing spondylitis: Adults: Administer 15 mg of this medicine orally once daily. The dose may be reduced to 7.5 mg per day according to the response to treatment. This medicine should not be administered at a dose exceeding 15 mg per day and should be taken with water or another beverage during a meal. For elderly patients or those at increased risk of adverse reactions, treatment is usually initiated at a dose of 7.5 mg per day. Patients with severe renal failure receiving hemodialysis should not receive more than 7.5 mg per day.

Individuals who regularly consume more than three drinks a day must consult a doctor or pharmacist before taking this medication. There is an increased risk of gastrointestinal bleeding if alcohol is consumed while taking this medication. This medication can affect the cardiovascular system, potentially increasing the risk of myocardial infarction or stroke. Individuals with cardiovascular disease or risk factors must be particularly cautious and should discontinue use immediately if they experience chest pain or shortness of breath. This medication can burden the stomach and may cause serious gastrointestinal issues such as gastric ulcers, bleeding, or perforation. Particularly, elderly patients or those with a history of gastrointestinal disorders should closely monitor for gastrointestinal symptoms during treatment, and seek medical advice immediately if any abnormal symptoms occur. This medication can cause serious allergic reactions in the skin, so if skin rashes or mucosal damage occur, treatment should be discontinued and medical professionals notified right away. It may affect kidney and liver function, so individuals with suspected or diagnosed kidney or liver diseases should undergo regular check-ups while taking this medication. Women planning to become pregnant or who have the possibility of being pregnant should not take this medication, and it absolutely should not be taken during pregnancy. Individuals who cannot break down lactose due to certain genetic issues should not take this medication. This medication has many interactions with other drugs, so it is essential to inform healthcare professionals about any other medications currently being taken. Dizziness, drowsiness, or blurred vision may occur while taking this medication, so caution should be exercised when driving or operating machinery. In case of overdose, symptoms such as nausea, vomiting, and gastrointestinal bleeding may arise, so care should be taken not to exceed the dosage, and if an overdose occurs, immediate medical attention should be sought. This medication should be kept out of the reach of children and stored in its original container to maintain quality.

• Gastrointestinal bleeding
• cardiovascular thrombotic reactions
• myocardial infarction
• stroke
• gastrointestinal or intestinal bleeding
• ulcers
• perforation
• exfoliative dermatitis
• mucous membrane syndrome
• toxic epidermal necrolysis

This medication may be sensitive to air and moisture, so it should be stored in a tightly closed container. The recommended storage temperature is room temperature between 1°C and 30°C. This will help maintain the drug's efficacy and safety for a long time.

Appearance

A capsule containing a slightly yellowish powder with a dark green outer and inner shell.

Package unit

30 capsules/bottle, 300 capsules/bottle