Melcam Capsule (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 gastric bleeding in individuals who regularly consume more than three glasses of alcohol daily, so it is essential to consult a doctor or pharmacist before taking it. This drug can increase the risk of cardiovascular disease, so patients with heart disease or risk factors must carefully monitor symptoms, and if symptoms such as chest pain or shortness of breath occur, they should stop taking it immediately. This drug can cause severe gastrointestinal side effects such as gastric bleeding, ulcers, and perforations; therefore, special caution is required for elderly patients or those with a history of gastrointestinal disorders. Serious allergic reactions on the skin or symptoms like rash and mucosal damage may occur, so if these symptoms appear, the medication should be stopped immediately. This medication may affect liver and kidney function; patients with liver or kidney diseases must undergo regular examinations and discontinue use if any abnormalities arise. Women planning to become pregnant or who may be pregnant should not take this medication, as it may reduce fertility and requires caution. This drug should not be administered to specific allergic patients, those with gastrointestinal bleeding, severe liver dysfunction, kidney dysfunction, heart failure, hypertension, adolescents under 15, pregnant or lactating women. Elderly patients may experience more severe reactions due to diminished bodily functions, so they should take the minimum dose with caution. While taking this medication, the risk of bleeding may increase if used in combination with other non-steroidal anti-inflammatory drugs, aspirin, anticoagulants, etc., so it is essential to consult a professional. In case of overdose, symptoms such as nausea, vomiting, gastric bleeding, and in severe cases, kidney failure or heart problems may occur, thus, immediate medical attention is necessary, and as there is no antidote, it is important to receive treatment according to the symptoms. This medication should be kept out of the reach of children and stored sealed in its original container.

Gastrointestinal bleeding, serious cardiovascular thrombotic reactions, myocardial infarction, stroke, bleeding from 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, elevated plasma creatinine, increased blood urea nitrogen, aplastic anemia, bone marrow suppression, changes in blood cell count, leukopenia, thrombocytopenia, anemia, decreased plasma iron, decreased hemoglobin, reduced hematocrit, increased neutrophils, increased eosinophils, increased basophils, increased monocytes, agranulocytosis, anaphylaxis, anaphylactoid reactions, discomfort, confusion, loss of orientation, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, nervousness, dizziness, drowsiness, headache, cephalalgia, fatigue, lethargy, taste dysfunction, mental stupor, seizures, 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 pectoris, heart failure, vasculitis, cough, upper respiratory infection, asthma, bronchospasm, shortness of breath, dyspepsia, nausea, vomiting, abdominal pain, constipation, bloating, diarrhea, loss of appetite, peptic ulcer, occult gastrointestinal bleeding, gross gastrointestinal bleeding, stomatitis, gastritis, esophagitis, belching, dry mouth, thirst, angular cheilitis, occult blood in stool, gastric perforation, colitis, pancreatitis, melena, perforated peptic ulcer, hepatitis, elevated plasma transaminase levels, increased bilirubin, jaundice, liver failure, alopecia, increased sweating, skin rash, urticaria, angioedema, vesicular dermatitis, erythema multiforme, photosensitivity reactions, contact dermatitis, fixed drug eruption, urination disorders, increased plasma creatinine levels, increased urea levels, decreased total protein, decreased albumin, proteinuria, glycosuria, increased urinary sediment, hematuria, sodium and fluid retention, hyperkalemia, acute renal failure, decreased urine output, frequency of urination, urinary tract infection, interstitial nephritis, edema, lower limb edema, fatigue, fever, facial edema, syncope, weight loss, weight gain, armpit and breast pain, arthralgia, low back pain, armpit and chest pain, stiffness, weakness in the legs, decreased female fertility, 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 and kept at room temperature between 1 degree and 30 degrees Celsius. By doing so, the efficacy of the drug will be maintained, and deterioration will be prevented.

Appearance

Hard capsules with greenish-brown color filled with yellow powder

Package unit

30 capsules/bottle, 300 capsules/bottle