CEMLOX Capsule 7.5 mg (Meloxicam)

Adult dose

1. Acute exacerbation of osteoarthritis (degenerative arthritis): ○ Adults: The usual dose is 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: The usual dose is 15 mg of this medicine orally once daily. Depending on the response to treatment, the dose may be reduced to 7.5 mg per day. Do not administer more than 15 mg per day. Take this medicine with water or another beverage during a meal. ○ In elderly patients or those at increased risk of adverse reactions, treatment is generally initiated at a dose of 7.5 mg per day. ○ Patients with severe renal impairment who are receiving hemodialysis should not receive more than 7.5 mg per day.

This medication may cause gastrointestinal bleeding if taken regularly by individuals who consume more than three alcoholic beverages per day, so consultation with a doctor or pharmacist is essential. It may increase the risk of serious cardiovascular problems such as myocardial infarction or stroke in individuals with cardiovascular diseases or risk factors, so caution is necessary. Serious gastrointestinal issues such as gastrointestinal bleeding, ulcers, or perforations may occur, so it should be used cautiously in elderly patients or those with a history of gastrointestinal diseases. This medication may cause serious skin reactions or allergic reactions, so if symptoms like rashes or mucosal damage occur, it should be discontinued immediately. It may affect kidney function, so individuals with kidney diseases or reduced kidney function should consult a doctor before use. This medication can also affect liver function, so if there are symptoms of liver dysfunction, it should be discontinued, and a doctor consulted. Pregnant women or those planning to become pregnant should avoid this medication, and it is also advised to avoid use during breastfeeding. It may interact with other medications, especially anticoagulants, diuretics, antihypertensives, lithium, and methotrexate, so consultation with a doctor is advisable when taken concurrently. Elderly patients may have decreased kidney and liver function, making adverse reactions more likely, so they should be cautious and start with the minimum dose. If dizziness, drowsiness, or blurriness of vision occurs while taking this medication, operating vehicles or machinery should be avoided. If any uncomfortable symptoms or adverse reactions occur during use, inform a doctor immediately for proper action.

Gastrointestinal bleeding, serious cardiovascular thrombotic reactions, myocardial infarction, stroke, bleeding of the stomach or intestines, ulcers, perforation, exfoliative dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis, anaphylactic reactions, interstitial nephritis, glomerulonephritis, renal medullary necrosis, nephrotic syndrome, elevated serum transaminases, increased liver function tests, increased plasma creatinine, increased blood urea nitrogen, aplastic anemia, bone marrow suppression, changes in blood cell count, leukopenia, thrombocytopenia, anemia, decreased plasma iron, decreased hemoglobin, decreased hematocrit, increased neutrophils, increased eosinophils, increased basophils, increased monocytes, agranulocytosis, anaphylaxis, anaphylactoid reactions, discomfort, confusion, loss of spatial orientation, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, irritability, dizziness, drowsiness, headache, cranial pressure, fatigue, lethargy, taste dysfunction, mental clouding, seizures, sensory disturbances, tremors, blurred vision, conjunctivitis, foreign body sensation in the eye, scleral hemorrhage, tinnitus, palpitations, elevated blood pressure, flushing, facial flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina, heart failure, vasculitis, cough, upper respiratory infection, asthma, bronchospasm, shortness of breath, allergic reactions to aspirin and other non-steroidal anti-inflammatory drugs, dyspepsia, nausea, vomiting, abdominal pain, constipation, bloating, diarrhea, loss of appetite, peptic ulcers, occult or visible gastrointestinal bleeding, stomatitis, gastritis, esophagitis, burping, dry mouth, thirst, angular cheilitis, occult blood in stool, gastrointestinal perforation, colitis, pancreatitis, melena, perforated peptic ulcer, hepatitis, elevated plasma transaminase levels, increased bilirubin, jaundice, liver failure, alopecia, increased sweating, skin rash, urticaria, itching, angioedema, vesicular dermatitis, erythema multiforme, photosensitivity reactions, contact dermatitis, fixed drug eruptions, urinary retention, elevated plasma creatinine levels, increased urea levels, decreased total protein, decreased albumin, proteinuria, glucosuria, increased urine sediment, hematuria, sodium and fluid retention, hyperkalemia, acute renal failure, decreased urine output, frequent urination, urinary tract infections, interstitial nephritis, edema, peripheral edema, fatigue, fever, facial edema, syncope, weight loss, weight gain, pain in the armpit and breast, arthralgia, low back pain, pain in the armpit and chest, stiffness, lower extremity weakness, diminished female reproductive capacity, dehydration, drowsiness, nausea, vomiting, epigastric pain, hypertension, acute renal failure, liver failure, respiratory depression, coma, seizures, cardiovascular collapse, cardiac arrest

This medication should be stored in a tightly sealed container that blocks light at a temperature between 1 and 30 degrees Celsius. Proper storage will maintain the medication's effectiveness and safety.

Appearance

A hard capsule with a dark green upper and lower part filled with light yellow contents.

Package unit

[For Domestic Use] 30 capsules/bottle, 300 capsules/bottle [For Export] 100 capsules/bottle