Moxicam Capsule (Meloxicam)

Adult dose

1. Acute exacerbations of osteoarthritis (degenerative arthritis): ○ Adults: Administer meloxicam 7.5 mg orally once daily. If symptoms do not improve, the dose may be increased to 15 mg daily as needed. 2. Rheumatoid arthritis, ankylosing spondylitis: ○ Adults: Administer 15 mg of this drug 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 drug per day. Take 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 failure receiving hemodialysis should not receive more than 7.5 mg daily.

This medication carries a risk of gastrointestinal bleeding in individuals who regularly consume three or more alcoholic drinks daily, thus it is crucial to consult with a doctor or pharmacist before use. Furthermore, this medication may affect the cardiovascular system, increasing the risk of serious cardiovascular diseases such as myocardial infarction or stroke. Those with pre-existing cardiovascular conditions or risk factors should exercise particular caution, and if symptoms such as chest pain or shortness of breath occur, they should stop taking the medication immediately. This medication can also affect the gastrointestinal tract, potentially leading to severe issues like bleeding, ulcers, or perforations in the stomach or intestines. Elderly patients or those with a history of gastrointestinal diseases should be particularly careful and should seek medical attention if gastrointestinal symptoms arise. Severe allergic reactions or serious skin reactions can occur, and if symptoms such as skin rash or mucosal damage develop, ingestion of the medication should be discontinued and healthcare personnel consulted. Since this medication can also affect kidney and liver function, caution is required for individuals with kidney or liver diseases or impaired function of these organs. Women who are planning to become pregnant or those who may be pregnant should not take this medication, as it may impact reproductive capacity. This medication should not be administered to individuals with specific allergy histories, children, pregnant women, nursing mothers, or patients with severe liver or kidney impairment. During treatment, it is important to have regular blood tests or liver and kidney function tests to detect any abnormalities early. In addition, due to significant interactions with other medications, it is essential to inform healthcare providers of any current medications being taken, especially if they include anticoagulants, diuretics, lithium, or methotrexate, as caution is required when used in combination. Care should be taken while driving or operating machinery as dizziness or drowsiness may occur. In cases of overdose, symptoms such as nausea, vomiting, or gastrointestinal bleeding may manifest, and immediate medical treatment is necessary. This medication should be kept out of the reach of children and stored in its original container, sealed appropriately.

Gastrointestinal bleeding, serious cardiovascular thrombotic reactions, myocardial infarction, stroke, exfoliative dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis, anaphylaxis, 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 changes, leukopenia, thrombocytopenia, anemia, decreased plasma iron, decreased hemoglobin, decreased hematocrit, neutrophilia, eosinophilia, basophilia, monocytosis, agranulocytosis, anaphylaxis, anaphylactoid reactions, discomfort, confusion, loss of directional sense, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, nervousness, dizziness, drowsiness, headache, cranial pressure, fatigue, lethargy, taste dysfunction, mental confusion, convulsions, sensory disturbances, tremors, blurred vision, conjunctivitis, foreign body sensation in the eye, tinnitus, palpitations, elevated blood pressure, flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina pectoris, heart failure, vasculitis, cough, upper respiratory tract infections, asthma, bronchospasm, shortness of breath, allergic reactions to aspirin and other non-steroidal anti-inflammatory drugs, 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, elevated plasma transaminase levels, elevated bilirubin, jaundice, liver failure, alopecia, increased sweating, skin rash, urticaria, angioedema, vesicular dermatitis, erythema multiforme, phototoxic reactions, contact dermatitis, fixed drug eruption, urinary retention, elevated plasma creatinine levels, elevated 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, fatigue, fever, facial edema, syncope, weight loss, weight gain, pain in armpits and breasts, arthralgia, low back pain, pain in armpits and chest, stiffness, lower limb weakness, decreased female reproductive capacity, 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 sealed container that blocks light. Additionally, it is important to store it at room temperature, specifically between 1 to 30 degrees Celsius, to maintain its effectiveness.

Appearance

Hard capsule filled with light yellow powder, with dark green upper and lower parts

Package unit

30 capsules/bottle, 300 capsules/bottle