Melocap Capsule 7.5 mg (Meloxicam)

Adult dose

1. Acute exacerbations 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 15 mg once 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 once daily according to the response to treatment. Do not administer more than 15 mg of this medicine per day. The entire daily dose should be taken 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 should usually be initiated at a dose of 7.5 mg once daily. ○ Patients with severe renal impairment receiving hemodialysis should not be given more than 7.5 mg once daily.

This medication can cause severe side effects such as gastrointestinal bleeding if taken by individuals who regularly consume more than three drinks a day; therefore, it is crucial to consult a doctor or pharmacist. This medication may affect the cardiovascular system and increase the risk of myocardial infarction or stroke, so patients with heart disease or those at risk should be particularly cautious. If symptoms such as chest pain, shortness of breath, weakness, or slurred speech occur while taking this medication, stop immediately and seek medical attention. This medication can cause serious issues like gastrointestinal bleeding, ulcers, and perforations. Patients, especially the elderly or those with a history of gastrointestinal diseases, should exercise caution. Severe allergic reactions or rashes may occur, and if there are any skin abnormality symptoms, consumption should stop immediately. This medication may affect kidney function, so patients with kidney disease or weakened kidney function should consult their doctor before taking it. Liver function abnormalities may occur; therefore, patients with liver disease require regular testing and should stop taking it if symptoms appear. Women who are pregnant or planning to become pregnant should not take this medication, and it should not be used while breastfeeding. There are many drug interactions; therefore, especially when taken with anticoagulants, diuretics, lithium, methotrexate, etc., consultation with a doctor is necessary. This medication may cause side effects such as drowsiness and dizziness, so caution is needed when driving or operating machinery. In case of overdose, gastric lavage and supportive treatment are needed, and there is no specific antidote, so caution is required. Store this medication out of reach of children, and keep it in its original container to maintain drug quality and safety.

Gastrointestinal bleeding, serious cardiovascular thromboembolic events, myocardial infarction, stroke, bleeding from the stomach or intestines, ulcers, perforation, exfoliative dermatitis, mucous membrane syndrome, toxic epidermal necrolysis, anaphylactic reactions, 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, changes in blood cell counts, leukopenia, thrombocytopenia, anemia, decreased plasma iron, reduced hemoglobin, decreased hematocrit, neutrophilia, eosinophilia, basophilia, monocytosis, agranulocytosis, anaphylaxis, anaphylactoid reactions, malaise, confusion, loss of orientation, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, neuroexcitability, dizziness, drowsiness, headache, cephalalgia, fatigue, lethargy, taste dysfunction, mental confusion, seizures, sensory disturbances, tremors, blurred vision, visual impairment, conjunctivitis, foreign body sensation in the eyes, subconjunctival hemorrhage, tinnitus, palpitations, elevated blood pressure, flushing, facial flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina pectoris, heart failure, vasculitis, cough, upper respiratory infection, asthma, bronchospasm, dyspnea, 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, jaundice, liver failure, alopecia, increased sweating, skin rash, urticaria, angioedema, vesicular dermatitis, erythema multiforme, photosensitive reactions, contact dermatitis, fixed drug eruption, urinary retention, elevated plasma creatinine, increased urea levels, proteinuria, glycosuria, increased urinary sediment, hematuria, sodium and fluid retention, hyperkalemia, acute renal failure, decreased urine output, urinary frequency, urinary tract infection, interstitial nephritis, edema, peripheral edema, malaise, fever, facial edema, syncope, weight loss, weight gain, axillary pain, breast pain, joint pain, low back pain, chest pain, rigidity, lower limb weakness, reduced female reproductive capacity, dehydration

This medication is sensitive to light, so it should be stored in a container that prevents light exposure. Additionally, it is best stored at room temperature between 1 and 30 degrees Celsius. Storing it this way can help maintain the medication's efficacy for a longer period.

Appearance

Hard capsules of light green color containing a pale yellow powder

Package unit

30 capsules/bottle, 300 capsules/bottle