Meloxicam Capsule 15 mg (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 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 the 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. ○ For older adults or patients at increased risk of adverse reactions, treatment is usually initiated at a dose of 7.5 mg daily. ○ Patients with severe renal failure undergoing hemodialysis should not receive more than 7.5 mg daily.

This medication poses a risk of gastrointestinal bleeding if taken by individuals who regularly consume more than three alcoholic beverages daily, hence consultation with a doctor or pharmacist is essential. This medication may affect the cardiovascular system, increasing the risk of serious cardiovascular diseases such as myocardial infarction or stroke; thus, careful monitoring is required, especially in those with a history of cardiovascular diseases or risk factors. Serious issues may arise, including gastrointestinal bleeding, ulcers, and perforations; therefore, individuals with a history of gastrointestinal diseases or elderly patients should consult a doctor before use. Severe allergic reactions or hypersensitivity may occur; if symptoms like skin rashes or mucosal damage appear, discontinue use immediately and consult healthcare professionals. As this medication may affect kidney and liver functions, regular testing is necessary for those who have kidney or liver issues or are on related medications. This medication may impair fertility; hence, women planning to conceive should avoid use, and pregnant or breastfeeding women should also refrain from using it. Individuals with specific allergies or hypersensitivity, history of gastrointestinal bleeding, severe liver or kidney disorders, heart failure, hypertension, or serious illnesses should not take this medication. Elderly patients may be more susceptible to the side effects of this medication, so it should be used cautiously at the minimal effective dose; caution is advised when driving or operating machinery as drowsiness or dizziness may occur. This medication may interact with others, so it is important to inform healthcare professionals when taken with anticoagulants, diuretics, lithium, methotrexate, etc., and regular checks are necessary. Overdose may result in symptoms such as nausea, vomiting, drowsiness, gastrointestinal bleeding, and in severe cases, renal failure, hepatic failure, or heart problems; seek immediate medical attention.

Gastrointestinal bleeding, serious cardiovascular thromboembolic events, myocardial infarction, stroke, exfoliative dermatitis, Stevens-Johnson 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, blood cell count changes, leukopenia, thrombocytopenia, anemia, decreased plasma iron, reduced hemoglobin, reduced hematocrit, increased neutrophils, increased eosinophils, increased basophils, increased monocytes, agranulocytosis, anaphylaxis, discomfort, confusion, loss of directional sense, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, irritability, dizziness, drowsiness, headache, increased intracranial pressure, fatigue, lethargy, taste dysfunction, mental clouding, seizures, sensory disturbances, tremors, blurred vision, conjunctivitis, ocular foreign body sensation, tinnitus, palpitations, hypertension, flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina pectoris, heart failure, vasculitis, cough, upper respiratory tract infection, asthma, bronchospasm, dyspnea, allergic reactions, 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, bullous dermatitis, erythema multiforme, photosensitivity reaction, contact dermatitis, fixed drug eruption, oliguria, elevated plasma creatinine levels, increased urea levels, decreased total protein, decreased albumin, proteinuria, glucosuria, increased urinary sediment, hematuria, sodium and fluid retention, hyperkalemia, acute renal failure, decreased urine output, frequent urination, urinary tract infection, interstitial nephritis, edema, peripheral edema, lethargy, fever, facial swelling, syncope, weight loss, weight gain, axillary and breast pain, arthralgia, low back pain, axillary and chest pain, rigidity, lower limb weakness, decreased female fertility, dehydration, drowsiness, nausea, vomiting, epigastric pain, hypertension, acute renal failure, liver failure, respiratory depression, comatose state, seizures, cardiovascular collapse, cardiac arrest

This medication is light-sensitive and should be stored in a tightly sealed container protected from light. The storage temperature should be maintained between 1 and 30 degrees Celsius to preserve the effectiveness and safety of the medication.

Appearance

A hard capsule with a light yellow powder inside, with an upper light green and lower yellow appearance.

Package unit

30 capsules/bottle, 300 capsules/bottle