Movid 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 medicine 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 medicine daily. Take with water or another beverage during a meal. ○ In elderly patients or those at increased risk of adverse reactions, treatment is generally started at a dose of 7.5 mg daily. ○ Patients with severe renal failure receiving hemodialysis must not receive more than 7.5 mg daily.

This medication may pose a risk of gastrointestinal bleeding in individuals who regularly consume more than three alcoholic beverages daily, so consultation with a physician or pharmacist is necessary. This medication may increase the risk of cardiovascular diseases and can potentially lead to severe issues such as myocardial infarction or stroke, so patients with a history of cardiovascular disease or risk factors should exercise particular caution. If symptoms such as chest pain, shortness of breath, weakness, or stuttering occur during use, the medication must be discontinued immediately, and medical attention should be sought. This medication may cause serious gastrointestinal side effects such as gastrointestinal bleeding, ulcers, and perforation, and caution is needed for individuals with a history of gastrointestinal diseases or the elderly. If gastrointestinal symptoms or signs of bleeding appear, it is important to inform medical personnel immediately and undergo necessary examinations. This medication can lead to serious skin reactions and allergic reactions, so if skin rash, mucosal damage, or difficulty in breathing occur, usage should be stopped. It may affect liver and kidney functions, so individuals with liver or kidney disease or related symptoms should consult a physician. Women planning to become pregnant or potentially pregnant are advised against using this medication, as it may affect fertility. This medication should not be administered to patients with certain genetic metabolic disorders. Before taking this medication, it is essential to consult a physician about any allergy history, pre-existing conditions, and other medications being taken. Regular blood tests and liver and kidney function tests are required for long-term use, and any abnormalities should be reported immediately. This medication may cause drowsiness or dizziness while driving or operating machinery, caution is advised. In cases of overdose, gastric lavage and supportive therapy are necessary, and since no antidote is available, immediate medical attention should be sought in emergencies. Keep out of reach of children and store in the original container sealed.

Gastrointestinal bleeding, serious cardiovascular thrombotic reactions, myocardial infarction, stroke, bleeding of the stomach or intestines, ulcers, perforation, exfoliative dermatitis, mucocutaneous syndrome, toxic epidermal necrolysis, anaphylactic reactions, interstitial nephritis, glomerulonephritis, renal medullary necrosis, nephrotic syndrome, elevated serum transaminases, increased liver function tests, increased 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 sense of direction, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, nervous hyperactivity, dizziness, drowsiness, headache, intracranial pressure, fatigue, lethargy, taste dysfunction, mental confusion, convulsions, sensory disturbances, tremors, blurred vision, conjunctivitis, foreign body sensation in the eye, hemorrhage of the sclera, tinnitus, palpitations, elevated blood pressure, flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina, heart failure, vasculitis, cough, upper respiratory tract infection, asthma, bronchial spasm, dyspnea, 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, cheilitis, fecal occult blood, 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 reactions, contact dermatitis, fixed drug eruption, urinary disorders, proteinuria, glucosuria, increased urine sediment, hematuria, sodium and fluid retention, hyperkalemia, acute renal failure, decreased urine output, frequency of urination, urinary tract infection, interstitial nephritis, edema, peripheral edema, malaise, fever, facial edema, syncope, weight loss, weight gain, breast and axillary pain, arthralgia, low back pain, axillary and chest pain, rigidity, lower limb weakness, reduced female fertility, dehydration

This medication should be stored in a tightly sealed container protected from light, at room temperature between 1 degree and 30 degrees Celsius. Proper storage ensures the maintenance of the medication's efficacy and safe use.

Appearance

Hard capsules with dark green upper and lower parts filled with pale yellow powder

Package unit

30 capsules/bottle, 300 capsules/bottle