Mobiden Capsule (Meloxicam)

Adult dose

1. Acute exacerbation 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 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 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 elderly patients or those at increased risk of adverse reactions, treatment is usually started at a dose of 7.5 mg per day. ○ Patients with severe renal failure receiving hemodialysis should not receive more than 7.5 mg per day.

This medicine may cause gastric bleeding if taken by individuals who regularly consume more than three alcoholic drinks daily; therefore, consultation with a physician or pharmacist is essential. Non-steroidal anti-inflammatory drugs, including this medication, may increase the risk of cardiovascular diseases; serious issues such as myocardial infarction or stroke may occur, so caution is particularly necessary for those with cardiovascular diseases or risk factors. If symptoms such as chest pain, shortness of breath, weakness, or stuttering appear while taking this medication, stop taking it immediately and consult with a healthcare professional. This medication can cause serious gastrointestinal adverse effects such as gastric bleeding, ulcers, and perforations; thus, those with a history of gastrointestinal diseases or the elderly should exercise increased caution. If gastrointestinal-related symptoms occur, inform a healthcare professional immediately and undergo necessary examinations; in severe cases, discontinuation of the medication may be required. This medication can cause serious skin reactions such as severe allergic reactions, dermatitis, or mucosal damage, so if a rash or mucosal damage occurs, stop taking it immediately. It may affect kidney function; therefore, patients with kidney disease or hypertension, heart failure should closely monitor kidney function while taking it. Women who are pregnant or may become pregnant should not take this medication, and it is advisable to avoid it even when planning for pregnancy. This medication should not be administered to breastfeeding women. If there is a hypersensitivity to this medication or allergies to aspirin or other non-steroidal anti-inflammatory drugs, it should not be used. The elderly may experience weakened kidney, liver, or heart functions, so it should be taken cautiously at the minimum dose, and special care should be taken regarding adverse reactions. This medication has significant interactions with other drugs, and caution is necessary when taken with anticoagulants, lithium, methotrexate, diuretics, antihypertensives, etc., and it is important to consult with healthcare professionals during use. In case of overdose, symptoms may include drowsiness, nausea, vomiting, gastric bleeding, and in severe cases, renal failure, liver failure, and a coma may occur; therefore, appropriate treatment should be sought immediately at a medical facility. This medication should be taken at the minimum effective dose for the shortest duration possible, and it is essential to undergo regular blood tests and examinations of liver and kidney functions to monitor for abnormalities. If symptoms like visual disturbances, dizziness, or drowsiness occur while taking this medication, avoid driving or operating machinery. This medication should be stored out of the reach of children, and kept sealed in its original container.

Gastrointestinal bleeding, cardiovascular thrombotic reactions, myocardial infarction, stroke, bleeding from the stomach or intestines, ulcers, perforation, exfoliative dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis, anaphylactic reaction, interstitial nephritis, glomerulonephritis, renal medullary necrosis, nephrotic syndrome, elevated serum transaminases, elevated liver function tests, increased plasma creatinine, increased blood urea nitrogen, aplastic anemia, bone marrow suppression, blood cell count changes, leukopenia, thrombocytopenia, anemia, decreased plasma iron, decreased hemoglobin, decreased hematocrit, increased neutrophils, increased eosinophils, increased basophils, increased monocytes, agranulocytosis, anaphylaxis, anaphylactoid reaction, discomfort, confusion, loss of directional sense, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, nervous irritability, dizziness, drowsiness, headache, head heaviness, fatigue, lethargy, taste dysfunction, mental cloudiness, convulsions, sensory disturbances, tremors, blurred vision, visual impairment, conjunctivitis, foreign body sensation in the eye, subconjunctival hemorrhage, tinnitus, palpitations, increased blood pressure, flushing, facial flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina, heart failure, vasculitis, cough, upper respiratory infection, asthma, bronchial spasm, dyspnea, 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, gross 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, skin rash, urticaria, itching, angioedema, vesicular dermatitis, erythema multiforme, photosensitive reactions, contact dermatitis, fixed drug eruption, urinary retention, elevated plasma creatinine levels, elevated urea levels, decreased total protein, decreased albumin, proteinuria, glycosuria, 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, fatigue, fever, facial swelling, syncope, weight loss, weight gain, axillary pain, breast pain, joint pain, lower back pain, axillary pain, chest pain, 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 may be light-sensitive, so it should be stored in an airtight container that blocks light. The storage temperature should be maintained between 1 degree and 30 degrees Celsius at room temperature. Proper storage will help maintain the efficacy and safety of the medication.

Appearance

Hard capsules of green color filled with yellow powder

Package unit

30 capsules/bottle, 300 capsules/bottle