Melodex Capsule 7.5mg (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 meloxicam orally once daily. The dose may be reduced to 7.5 mg per day according to response to treatment. Do not administer more than 15 mg per day. Take the daily dose all at once, with water or another beverage during a meal. ○ For older adults or those at increased risk of adverse reactions (e.g., history of gastrointestinal disease or cardiovascular risk factors), treatment is usually initiated at a dose of 7.5 mg per day. ○ Patients with severe renal impairment receiving hemodialysis should not receive more than 7.5 mg per day.

Individuals who regularly consume more than three alcoholic beverages per day should consult with a doctor or pharmacist before taking this medication. There is a risk of gastrointestinal bleeding when taken with alcohol. This medication may affect the cardiovascular system, so patients with heart disease or cardiovascular risk factors should exercise caution. If symptoms such as chest pain, shortness of breath, weakness, or slurred speech occur, discontinue use immediately. This medication can cause serious issues such as gastrointestinal bleeding, ulcers, or perforation, so special care should be taken in patients with a history of gastrointestinal diseases or the elderly. The risk may increase with prolonged use. Severe reactions may occur on the skin; therefore, if symptoms such as rash, blisters, or mucosal damage occur, discontinue the medication immediately and consult a healthcare provider. Since it may affect kidney and liver function, inform your healthcare provider if you have kidney or liver disease or related symptoms. Blood tests or kidney function tests may be necessary. Women who are pregnant or planning to become pregnant should not take this medication, and nursing mothers should also avoid using it. This medication may affect fertility. This medication should not be given to patients with specific allergies, asthma, or a history of gastrointestinal bleeding, and should be avoided if there is a hypersensitivity to the medication. As there are many potential drug interactions, especially with anticoagulants, diuretics, antihypertensive drugs, lithium, methotrexate, etc., consultation with a healthcare provider and careful monitoring are required, especially when taken together. If symptoms such as drowsiness, dizziness, or blurred vision occur, avoid driving or operating machinery. When using this medication long-term, regular blood tests and liver, kidney function tests should be performed, and if any abnormal symptoms appear, notify your healthcare provider immediately. In case of overdose, symptoms such as nausea, vomiting, and gastrointestinal bleeding may occur, and in severe cases, renal failure, liver failure, or coma may develop, so immediate emergency treatment is required. This medication should be kept out of the reach of children, and should be stored in its original sealed container.

Gastrointestinal bleeding, severe cardiovascular thrombotic reaction, myocardial infarction, stroke, bleeding from the stomach or intestines, ulcers, perforation, exfoliative dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis, anaphylaxis, interstitial nephritis, glomerulonephritis, renal medullary necrosis, nephrotic syndrome, elevated serum transaminases, elevated liver function tests, 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, decreased hematocrit, increased neutrophils, increased eosinophils, increased basophils, increased monocytes, agranulocytosis, anaphylaxis, anaphylactoid reactions, malaise, confusion, loss of orientation, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, irritability, dizziness, drowsiness, headache, cranial pressure, fatigue, lethargy, taste dysfunction, mental confusion, seizures, sensory abnormalities, tremor, blurred vision, visual impairment, conjunctivitis, foreign body sensation in the eye, hemorrhage in the sclera of the eye, 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, dyspepsia, nausea, vomiting, abdominal pain, constipation, bloating, diarrhea, anorexia, peptic ulcer, occult gastrointestinal bleeding, gross gastrointestinal bleeding, stomatitis, gastritis, esophagitis, belching, dry mouth, thirst, angular cheilitis, occult blood in stool, gastrointestinal perforation, colitis, pancreatitis, melena, perforated peptic ulcer, hepatitis, elevated plasma transaminase levels, elevated bilirubin, jaundice, liver failure, alopecia, increased sweating, skin rash, urticaria, pruritus, angioedema, vesicular dermatitis, erythema multiforme, photosensitive reactions, contact dermatitis, fixed drug eruption, urinary disorders, elevated plasma creatinine levels, elevated urea levels, decreased total protein, decreased albumin, proteinuria, glucosuria, increased urine sediment, hematuria, sodium and water retention, hyperkalemia, acute renal failure, decreased urine output, frequent urination, urinary tract infection, interstitial nephritis, edema, peripheral edema, fatigue, 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 reproductive ability, dehydration, drowsiness, nausea, vomiting, epigastric pain, hypertension, acute renal failure, liver failure, respiratory depression, comatose state, seizures, cardiovascular collapse, cardiac arrest

This medication may be sensitive to light, so it should be stored in a tightly closed container that blocks light. Additionally, it is important to store the medication at room temperature between 1°C to 30°C to maintain its effectiveness.

Appearance

A hard capsule containing a light yellow powder with a pale green outer shell.

Package unit

30 capsules/bottle, 300 capsules/bottle