Exicam Capsule 7.5 mg (Meloxicam)

Adult dose

1. Acute exacerbation 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. 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 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 patients at increased risk of adverse reactions, treatment is usually initiated at a dose of 7.5 mg per day. ○ Patients with severe renal failure undergoing hemodialysis should not receive more than 7.5 mg per day.

This medication may cause gastrointestinal bleeding if taken by individuals who regularly consume more than three glasses of alcohol daily; therefore, it is essential to consult a doctor or pharmacist. This medication may increase the risk of cardiovascular diseases and may lead to serious issues, such as heart attack or stroke, especially in individuals with existing cardiovascular conditions or risk factors; therefore, careful monitoring is necessary. This medication can cause serious adverse reactions such as gastrointestinal bleeding, ulcers, and perforations, so individuals with a history of gastrointestinal diseases or the elderly should be particularly cautious and should consult a doctor immediately if gastrointestinal symptoms appear. This medication may cause severe skin reactions or life-threatening allergic reactions; therefore, if symptoms such as skin rashes or mucosal damage occur, discontinue use immediately. It may affect kidney and liver function; therefore, individuals with kidney or liver problems should consult a doctor before taking this medication and should undergo regular check-ups while taking it. This medication may decrease fertility; therefore, women planning to become pregnant should avoid using it, and pregnant or nursing women should also refrain from taking it. Individuals who have previously had allergic reactions to this medication or similar drugs, or have a history of asthma or severe gastrointestinal disease, should not take this medication. This medication may cause symptoms such as drowsiness and dizziness, necessitating caution when driving or operating machinery. There may be interactions with other medications; therefore, individuals currently taking any medication should inform their doctor or pharmacist, particularly when taking anticoagulants, diuretics, hypertension medications, lithium, or methotrexate. Long-term use of this medication requires regular blood tests, liver function tests, and kidney function tests; if any abnormal symptoms occur, consult a healthcare professional immediately. In case of overdose, symptoms such as nausea, vomiting, gastrointestinal bleeding, or severe cases of renal failure or heart problems may occur; seek emergency treatment if suspected. Store this medication out of reach of children and ensure it is sealed in its original container to maintain its quality.

• Gastrointestinal bleeding
• cardiovascular thrombotic reactions
• myocardial infarction
• stroke
• bleeding from the stomach or intestines
• ulcers
• perforation
• exfoliative dermatitis
• Stevens-Johnson syndrome
• toxic epidermal necrolysis

This medication should be stored in a light-blocking container, as it is sensitive to light. It should also be stored at room temperature between 1 degree and 30 degrees Celsius to maintain its effectiveness.

Appearance

A hard capsule with a light green-yellow powder filled inside.

Package unit

30 capsules/bottle, 100 capsules/bottle