CMG Meloxicam Capsule 15 mg

Adult dose

1. Acute exacerbation of osteoarthritis (degenerative arthritis): ○ Adults: Administer meloxicam 7.5 mg orally once daily. If symptoms do not improve, the dose may be increased to 15 mg per day as needed. 2. 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 depending on the response to treatment. Do not administer more than 15 mg of this medicine per day. Take it 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.

This medication must be discussed with a doctor or pharmacist before use by individuals who regularly consume alcohol above a certain amount daily because it may pose a risk of gastrointestinal bleeding. This medication may increase the risk of cardiovascular problems, including serious issues such as heart attacks or strokes. Therefore, extra caution is needed, especially if there are existing cardiovascular diseases or risk factors. If symptoms such as chest pain, shortness of breath, weakness, or slurred speech occur during use, discontinue the medication immediately and consult a doctor. This medication may cause serious gastrointestinal issues such as bleeding, ulcers, or perforation, with the risk being greater for older patients or those with a history of gastrointestinal diseases. Immediate medical evaluation and treatment are required if gastrointestinal symptoms appear, and in severe cases, medication may need to be discontinued. This medication can cause severe skin reactions and allergic reactions; thus, use should be discontinued immediately if any abnormal skin symptoms occur. It may affect kidney function, so patients with kidney disease or impaired kidney function should be cautious. Liver function levels may temporarily rise, so those with liver disease or symptoms of liver dysfunction should consult a doctor. Women planning to become pregnant are advised not to use this medication, and it should especially not be administered during pregnancy. Individuals with a history of allergy to this medication or similar medications, those with a history of gastrointestinal bleeding or ulcers, severe liver or kidney disease patients, or patients with severe heart failure or high blood pressure should not use this medication. Older adults should take it cautiously at the minimum dosage due to possible impaired kidney and liver function, paying attention to adverse reactions. Drug interactions may occur, so it is essential to inform your doctor or pharmacist if taking anticoagulants, lithium, methotrexate, diuretics, or antihypertensives. If drowsiness, dizziness, or visual disturbances occur during use, individuals should avoid driving or operating machinery. Patients using this medication long-term require regular blood tests and liver and kidney function assessments, and should immediately consult a healthcare professional if abnormal symptoms arise. In overdose cases, gastric lavage and supportive treatment are necessary; as there is no antidote, emergency care must be sought. This medication should be kept out of the reach of children and securely stored in its original container.

• Gastrointestinal bleeding
• serious cardiovascular thrombotic events
• myocardial infarction
• stroke
• bleeding from the stomach or intestines
• ulcers
• perforation
• exfoliative dermatitis
• mucous membrane syndrome
• toxic epidermal necrolysis

This medication is sensitive to light and should be stored in a container that blocks light. Additionally, it is essential to keep it at room temperature, between 1 and 30 degrees Celsius, to maintain its effectiveness.

Appearance

A capsule with a dark green upper part and a yellow lower part containing a pale yellow powder

Package unit

Bottle packaging: 100 capsules, 30 capsules