Mobic Capsule 7.5 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 meloxicam orally once daily. The dose may be reduced to 7.5 mg daily according to response to treatment. Do not administer more than 15 mg of this drug per day. The daily dose should be taken all at once, with water or another beverage during a meal. ○ In elderly patients or those at increased risk of adverse reactions (e.g., a history of gastrointestinal disease or cardiovascular risk factors), treatment is usually initiated at a dose of 7.5 mg daily. ○ Patients with severe renal impairment receiving hemodialysis should not be given more than 7.5 mg daily.

This medication may increase the risk of gastrointestinal bleeding in individuals who regularly consume more than three alcoholic beverages per day, so it is essential to consult a doctor or pharmacist before use. This medication may affect the cardiovascular system and increase the risk of serious cardiovascular events such as myocardial infarction or stroke. Individuals with a history of cardiovascular disease or risk factors should be especially cautious, and if symptoms such as chest pain, shortness of breath, weakness, or slurred speech occur, they should stop taking the medication immediately. This medication can cause serious gastrointestinal side effects such as gastrointestinal bleeding, ulcers, or perforation. Older adults or those with a history of gastrointestinal diseases should exercise increased caution and seek immediate medical attention if gastrointestinal bleeding symptoms are suspected. This medication may cause severe skin reactions and allergic reactions, so if any abnormal symptoms such as skin rash or mucosal damage occur, stop taking it immediately. It may affect kidney function; therefore, individuals with kidney disease or those taking diuretics or antihypertensive medications should monitor their kidney function regularly while using this medication. This medication may harm the fetus during pregnancy, so women who are pregnant or planning to become pregnant should not use it, and breastfeeding women should also avoid taking it. Older adults may have reduced liver, kidney, and heart function, so they should take the minimum effective dose carefully and monitor for any adverse reactions. This medication can interact with other NSAIDs, anticoagulants, diuretics, and antihypertensive medications, so individuals taking other medications must inform their doctor or pharmacist. Overdose may cause symptoms such as nausea, vomiting, drowsiness, and gastrointestinal bleeding, requiring immediate medical attention for gastric lavage and appropriate treatment. Keep this medication out of the reach of children and store it securely in its original container.

Gastrointestinal hemorrhage, serious cardiovascular thrombotic reaction, myocardial infarction, stroke, bleeding from the stomach or intestines, ulcer, perforation, exfoliative dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis, anaphylactic reaction, interstitial nephritis, glomerulonephritis, renal medullary necrosis, nephrotic syndrome, elevation of serum transaminases, liver function test elevation, increase in plasma creatinine, increase in blood urea nitrogen, aplastic anemia, bone marrow suppression, changes in blood cell counts, leukopenia, thrombocytopenia, anemia, decreased serum iron, hemoglobin reduction, decreased hematocrit level, neutrophilia, eosinophilia, basophilia, monocytosis, agranulocytosis, anaphylaxis, malaise, confusion, loss of orientation, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, neuroexcitability, dizziness, drowsiness, headache, cranial discomfort, fatigue, lethargy, dysgeusia, mental confusion, convulsions, sensory disturbances, tremor, blurred vision, conjunctivitis, foreign body sensation in the eyes, subconjunctival hemorrhage, tinnitus, palpitations, increased blood pressure, flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina, heart failure, vasculitis, cough, upper respiratory infection, asthma, bronchospasm, dyspnea, dyspepsia, nausea, vomiting, abdominal pain, constipation, distention, diarrhea, anorexia, peptic ulcer, occult gastrointestinal bleeding, gross gastrointestinal bleeding, stomatitis, gastritis, esophagitis, belching, dry mouth, angular cheilitis, occult blood in urine, gastrointestinal perforation, colitis, pancreatitis, melena, perforated peptic ulcer, hepatitis, jaundice, liver failure, alopecia, increased sweating, skin rash, urticaria, itching, angioedema, vesicular dermatitis, erythema multiforme, photosensitivity reaction, contact dermatitis, fixed drug eruption, urinary retention, increased plasma creatinine, elevated urea level, decreased total protein, reduced albumin, proteinuria, glucosuria, increased urine sediments, hematuria, sodium and fluid retention, hyperkalemia, acute renal failure, decreased urine output, polyuria, urinary tract infection, interstitial nephritis, edema, lower limb edema, malaise, fever, facial swelling, syncope, weight loss, weight gain, armpit and breast pain, arthralgia, low back pain, armpit and chest pain, stiffness, weakness of the lower limbs, female infertility, delayed ovulation, dehydration, drowsiness, nausea, vomiting, epigastric pain, hypertension, acute renal failure, liver failure, respiratory depression, coma, convulsion, cardiovascular collapse, cardiac arrest

This medication is sensitive to air and humidity, so it should be stored in a tightly sealed container. It is optimal to store it at room temperature between 1 and 30 degrees Celsius. Proper storage will help maintain the effectiveness of the medication for an extended period.

Appearance

A capsule with yellow powder inside, bright green cap and body

Package unit

100 capsules (10 capsules/PTP x 10)