Megaroxicam Capsule 15 mg (Meloxicam)

Adult dose

1. Acute exacerbation of osteoarthritis (degenerative joint disease): ○ Adults: Administer meloxicam 7.5 mg orally once daily. If symptoms do not improve, the dose may be increased to up 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 daily. 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 failure receiving hemodialysis should not receive more than 7.5 mg daily.

This medication should be used with caution for individuals who regularly consume more than three alcoholic drinks a day due to an increased risk of gastrointestinal bleeding, and they must consult a physician or pharmacist. It can affect the cardiovascular system and may pose risks for serious issues such as heart attack or stroke, so special caution is required for individuals with or at risk for cardiovascular diseases. Those with a history of gastric ulcers or bleeding should be careful, as serious side effects such as gastrointestinal bleeding or perforation may occur when taking this medication. Serious allergic reactions can occur, so if symptoms like skin rash or mucosal damage appear, discontinue use immediately. This medication may affect kidney function; hence, individuals with kidney disease or weak kidney function should periodically monitor their kidney condition while taking this medication. It can temporarily elevate liver function levels, and individuals with liver disease or signs of liver dysfunction should consult a physician. Women planning or possibly pregnant should avoid this medication, and it should never be taken during pregnancy. This medication is not to be administered to children under 15, and elderly patients should use the lowest dose cautiously due to potential weak kidney and liver function. Combining with other non-steroidal anti-inflammatory drugs may increase the risk of side effects, so consultation with a professional is necessary before taking. If symptoms such as dizziness, drowsiness, or blurred vision occur during use, it is safest to avoid driving or operating machinery. In case of overdose, severe symptoms such as nausea, vomiting, and gastrointestinal bleeding may occur, so the prescribed dose must be adhered to, and immediate medical attention is required in case of overdose. This medication should be stored out of the reach of children and kept in the original container for safety.

Gastrointestinal bleeding, serious cardiovascular thrombotic reactions, myocardial infarction, stroke, exfoliative dermatitis, mucous membrane syndrome, toxic epidermal necrolysis, anaphylaxis reaction, interstitial nephritis, glomerulonephritis, renal medullary necrosis, nephrotic syndrome, serum transaminase elevation, liver function test elevation, plasma creatinine increase, blood urea nitrogen increase, aplastic anemia, bone marrow suppression, blood cell count changes, leukopenia, thrombocytopenia, anemia, plasma iron decrease, hemoglobin decrease, hematocrit decrease, neutrophilia, eosinophilia, basophilia, monocytosis, agranulocytosis, anaphylaxis, anaphylactoid reactions, discomfort, confusion, loss of direction sense, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, hypersensitivity, dizziness, drowsiness, headache, cranial pressure, 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, facial flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina pectoris, heart failure, vasculitis, cough, upper respiratory infection, asthma, bronchospasm, respiratory distress, dyspepsia, nausea, vomiting, abdominal pain, constipation, bloating, diarrhea, loss of appetite, peptic ulcer, occult gastrointestinal bleeding, visible gastrointestinal bleeding, stomatitis, gastritis, esophagitis, belching, dry mouth, thirst, angular cheilitis, occult blood in stool, gastrointestinal perforation, colitis, pancreatitis, melena, perforated peptic ulcer, hepatitis, angioedema, vesicular dermatitis, erythema multiforme, photosensitivity reactions, contact dermatitis, fixed drug eruption, urinary retention, elevated plasma creatinine level, increased urea level, decreased total protein, decreased albumin, proteinuria, glucosuria, increased urinary sediment, hematuria, sodium retention, fluid retention, hyperkalemia, acute renal failure, reduced urine output, frequent urination, urinary tract infection, interstitial nephritis, edema, lower limb edema, lethargy, fever, facial edema, syncope, weight loss, weight gain, axillary pain, breast pain, joint pain, low back pain, chest pain, stiffness, lower limb weakness, decreased female reproductive capacity, dehydration

This medication may be sensitive to light, so it should be stored in a dark, airtight container. It is advisable to keep the storage temperature between 1 and 30 degrees Celsius to maintain the effectiveness of the medication for an extended period.

Appearance

A hard capsule with a light green upper part and yellow lower part containing a pale yellow powder.

Package unit

30 capsules/bottle, 300 capsules/bottle