Meloxicam Capsule (Meloxicam)

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 daily 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 daily according to 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. ○ In elderly patients or those at increased risk of adverse reactions, treatment is usually initiated at a dose of 7.5 mg daily. ○ Patients with severe renal impairment receiving hemodialysis should not receive more than 7.5 mg daily.

This medication should be consulted with a doctor or pharmacist before use by individuals who regularly consume more than three drinks a day. Otherwise, gastrointestinal bleeding may occur. This medication can increase the risk of cardiovascular diseases, so individuals with a history of heart disease or stroke, or risk factors, should exercise extra caution. If symptoms such as chest pain, shortness of breath, weakness, or slurred speech occur during use, stop taking the medication immediately and consult a healthcare professional. This medication can cause serious gastrointestinal diseases such as gastrointestinal bleeding, ulcers, and perforation, so individuals with a history of gastrointestinal diseases or symptoms should be especially careful. Elderly patients may experience these side effects more severely. Severe allergic reactions on the skin, dermatitis, or mucosal damage may occur, so if skin rashes or abnormalities in mucous membranes appear, stop taking the medication immediately and inform a healthcare professional. This medication may affect kidney function, so individuals with kidney disease or impaired kidney function should be carefully monitored while taking it. Women planning to become pregnant or who may become pregnant should not use this medication, and women who are pregnant or breastfeeding should also avoid taking it. Like other non-steroidal anti-inflammatory drugs, this medication requires regular blood tests, liver function tests, and kidney function tests, and should consult a healthcare professional immediately if any abnormal symptoms occur. Additionally, this medication may interact with other drugs, so it is essential to inform about any current medications being taken. Drowsiness, dizziness, and visual disturbances may occur while taking this medication, so caution is required while driving or operating machinery. In case of overdose, gastric lavage or general supportive treatment may be necessary, as there is no specific antidote, follow medical advice. Finally, this medication should be kept out of the reach of children and stored in its original container for safety.

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

This medication is sensitive to light, so it should be stored in a dark place, preferably at room temperature between 1°C and 30°C. Storing it this way helps maintain its effectiveness for a longer period.

Appearance

A hard capsule filled with a light yellow content, with dark green upper and lower parts.

Package unit

30 capsules/bottle, 300 capsules/bottle