Unicox Capsule 7.5 mg (Meloxicam)

Adult dose

1. Acute exacerbations of osteoarthritis (degenerative arthritis): ○ Adults: Administer 7.5mg of meloxicam orally once daily. If symptoms do not improve, the dose may be increased to up to 15mg daily as needed. 2. Rheumatoid arthritis, ankylosing spondylitis: ○ Adults: Administer 15mg of this medicine orally once daily. The dose may be reduced to 7.5mg daily according to response to treatment. This medicine should not be administered at doses exceeding 15mg daily, and should be taken 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 7.5mg daily. ○ Patients with severe renal failure receiving hemodialysis should not receive more than 7.5mg daily.

This drug can cause gastrointestinal bleeding if taken by someone who regularly consumes more than three alcoholic beverages per day; therefore, consultation with a doctor or pharmacist is essential. This drug can affect the cardiovascular system, so patients with a history of cardiovascular disease or risk factors should be cautious, and if symptoms such as chest pain or shortness of breath occur, they should stop taking it immediately. This drug may cause serious gastrointestinal adverse reactions such as gastrointestinal bleeding, ulcers, or perforations; therefore, those with a history of gastrointestinal disease or the elderly should take extra care when using it. Severe allergic reactions or severe dermatitis may occur; thus, if skin rash or mucosal damage appears, use should be discontinued, and a doctor's consultation is required. This drug may affect kidney function, so patients with kidney disease or conditions like hypertension or heart failure should consult healthcare professionals before use and periodically check kidney function. Women who are pregnant or planning to become pregnant should not take this drug, and those who are breastfeeding should also avoid it. There may be interactions with other medications, so if you are currently taking any other drugs, you must inform healthcare professionals, especially when used in combination with anticoagulants, diuretics, lithium, or methotrexate. Long-term use requires regular blood tests and evaluations of liver and kidney function to detect and manage adverse reactions early. Symptoms such as dizziness or drowsiness may occur when driving or operating machinery, so caution is advised when such symptoms are present. If any abnormal symptoms or discomfort occur during use, consult a healthcare professional immediately and follow their guidance.

Gastrointestinal hemorrhage, serious cardiovascular thrombotic reactions, myocardial infarction, stroke, gastrointestinal or intestinal bleeding, ulcers, perforations, exfoliative dermatosis, mucocutaneous syndrome, toxic epidermal necrolysis, anaphylactic reactions, interstitial nephritis, glomerulonephritis, renal medullary necrosis, nephrotic syndrome, elevated serum transaminases, increased liver function values, increased plasma creatinine, increased blood urea nitrogen, aplastic anemia, bone marrow suppression, changes in blood cell counts, leukopenia, thrombocytopenia, anemia, decreased plasma iron, decreased hemoglobin, reduced hematocrit levels, neutrophilia, eosinophilia, basophilia, monocytosis, agranulocytosis, anaphylaxis, anaphylactoid reactions, malaise, confusion, loss of orientation, mood swings, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, nervous irritability, dizziness, drowsiness, headache, pressure in the head, fatigue, lethargy, taste dysfunction, mental confusion, convulsions, sensory abnormalities, tremors, blurred vision, conjunctivitis, foreign body sensation in the eye, subconjunctival hemorrhage, tinnitus, palpitations, elevated blood pressure, flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina, heart failure, vasculitis, cough, upper respiratory infections, asthma, bronchial spasm, shortness of breath, dyspepsia, nausea, vomiting, abdominal pain, constipation, bloating, diarrhea, loss of appetite, peptic ulcer, occult gastrointestinal bleeding, overt gastrointestinal bleeding, stomatitis, gastritis, esophagitis, belching, dry mouth, thirst, angular cheilitis, occult blood in stool, gastric perforation, colitis, pancreatitis, melena, perforated peptic ulcer, hepatitis, jaundice, liver failure, alopecia, increased sweating, skin rash, urticaria, angioedema, vesicular dermatitis, erythema multiforme, photosensitivity reactions, contact dermatitis, fixed drug eruption, urination disorders, elevated plasma creatinine levels, increased urea levels, decreased total protein, decreased albumin, proteinuria, glucosuria, increased urinary sediments, urinary hematuria, sodium and fluid retention, hyperkalemia, acute renal failure, decreased urine output, frequent urination, urinary tract infections, interstitial nephritis, edema, lower extremity edema, lethargy, fever, facial edema, syncope, weight loss, weight gain, axillary and breast pain, arthralgia, low back pain, axillary and chest pain, stiffness, lower limb weakness, decreased female fertility, dehydration

This drug is sensitive to light, so it should be stored in a sealed container that blocks light. It is important to maintain a storage temperature between 1 degree and 30 degrees Celsius.

Appearance

Capsule filled with pale yellow powder, dark green on the upper and lower parts

Package unit

30 capsules/bottle, 100 capsules/bottle, 300 capsules/bottle