Meloxicam Capsule (Meloxicam)

Adult dose

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 daily as needed. Rheumatoid arthritis, ankylosing spondylitis: ○ Adults: Administer 15 mg of this medication orally once daily. The dose may be reduced to 7.5 mg daily depending on the response to treatment. Do not administer more than 15 mg of this medication per day. Take it with water or another beverage during a meal. ○ For elderly patients or those at increased risk of adverse reactions, treatment is usually started at a dose of 7.5 mg daily. ○ Patients with severe renal impairment undergoing hemodialysis should not receive more than 7.5 mg daily.

This medication should be consulted with a doctor or pharmacist before use for individuals who regularly consume more than three alcoholic beverages a day. Heavy drinkers may have an increased risk of gastrointestinal bleeding when taking this medication. This medication may have effects on the cardiovascular system and may increase the risk of serious cardiovascular diseases such as myocardial infarction or stroke. Individuals with a history of cardiovascular disease or risk factors should carefully observe for cardiovascular symptoms while taking this medication, and if symptoms such as chest pain, shortness of breath, or slurred speech occur, the medication should be stopped immediately. This medication may increase the risk of serious gastrointestinal issues such as bleeding, ulcers, or perforations. Elderly individuals or those with a history of gastrointestinal disorders should exercise particular caution, and if symptoms of gastrointestinal pain or bleeding occur, immediate medical consultation is necessary. This medication can cause serious skin reactions and allergic reactions, so if symptoms such as skin rash or mucosal damage appear, the medication should be stopped immediately and the doctor should be consulted. This medication may affect kidney function and can occasionally lead to nephritis or decreased kidney function. Since liver function test values may increase, consult with a physician if unusual symptoms occur. This medication may decrease fertility, so women planning a pregnancy should avoid using it. Pregnant women, those who may become pregnant, and breastfeeding women should not take this medication. This medication should not be used in individuals with specific allergies, gastrointestinal bleeding, severe liver or kidney impairment, severe heart failure, severe hypertension, adolescents under 15, or patients with inflammatory bowel disease. Elderly individuals, those with a history of gastrointestinal disorders, patients with bleeding disorders, asthma patients, and individuals with cardiovascular disease risk factors should take this medication with caution, and should be monitored regularly for adverse reactions during treatment. This medication may interact with other anti-inflammatory analgesics, anticoagulants, diuretics, antihypertensives, etc., so if other medications are being taken, consult with a doctor or pharmacist. Drowsiness, dizziness, or blurred vision may occur during use, so caution is necessary when driving or operating machinery. In case of overdose, symptoms such as nausea, vomiting, gastrointestinal bleeding, decreased kidney function, or heart problems may occur, so do not exceed the prescribed dosage, and seek immediate medical attention if unusual symptoms arise. Store this medication out of reach of children and keep it in its original container. Transferring it to another container can pose a risk of misuse or quality deterioration, so care should be taken.

Gastrointestinal bleeding, serious cardiovascular thrombotic reactions, myocardial infarction, stroke, bleeding from the stomach or intestines, ulcer, perforation, exfoliative dermatitis, mucocutaneous syndrome, toxic epidermal necrolysis, anaphylaxis, 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 counts, leukopenia, thrombocytopenia, anemia, decreased plasma iron, decreased hemoglobin, decreased hematocrit, increased neutrophils, increased eosinophils, increased basophils, increased monocytes, agranulocytosis, anaphylaxis, malaise, confusion, loss of directional sense, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, neuroasthenia, dizziness, drowsiness, headache, cephalalgia, fatigue, lethargy, taste dysfunction, mental clouding, convulsions, sensory disturbances, tremor, blurry vision, conjunctivitis, foreign body sensation in the eye, scleral hemorrhage, tinnitus, palpitations, increased 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, decreased appetite, peptic ulcer, occult gastrointestinal bleeding, visible 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, pruritus, angioedema, vesicular dermatitis, erythema multiforme, photosensitivity reactions, contact dermatitis, fixed drug eruption, urination disorders, increased plasma creatinine levels, elevated urea levels, decreased total proteins, decreased albumin, proteinuria, glucosuria, 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, malaise, fever, facial edema, syncope, weight loss, weight gain, pain in armpit and breast, arthralgia, low back pain, pain in armpit and chest, stiffness, weakness in the lower limbs, decreased female reproductive ability, dehydration, drowsiness, nausea, vomiting, epigastric pain, hypertension, acute renal failure, liver failure, respiratory depression, coma, convulsions, cardiovascular collapse, cardiac arrest

This medication is sensitive to light, so it should be stored in a tightly closed container that blocks light. Additionally, it is best to store the medication at a temperature between 1 to 30 degrees Celsius. Storing it this way will help maintain the medication's effectiveness.

Appearance

Green capsule containing pale yellow powder

Package unit

Capsule/Bottle - 30 Capsules/Bottle, Capsule/Bottle - 300 Capsules/Bottle