Melocox Capsule 7.5 mg (Meloxicam)

Adult dose

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 daily as needed. Rheumatoid arthritis, ankylosing spondylitis: ○ Adults: Administer 15 mg of this medication 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 medication daily. Take with water or another beverage during a meal. ○ In 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 impairment undergoing hemodialysis should not receive more than 7.5 mg daily.

This medication should be discussed with a doctor or pharmacist if you regularly consume more than three alcoholic drinks a day, as it increases the risk of gastrointestinal bleeding. This medication may affect the cardiovascular system and increase the risk of serious thrombotic events such as myocardial infarction or stroke; therefore, individuals with cardiovascular conditions or risk factors should exercise caution. If you experience symptoms such as chest pain, shortness of breath, weakness, or slurred speech while taking this medication, stop taking it immediately and consult a healthcare provider. This non-steroidal anti-inflammatory drug may cause serious gastrointestinal issues such as bleeding, ulcers, or perforation, so those with a history of gastrointestinal disease or the elderly should exercise particular caution. This medication can cause severe allergic reactions, dermatitis, or significant skin abnormalities; if any unusual skin symptoms occur, use should be discontinued immediately. It may affect liver and kidney functions; therefore, those with liver or kidney diseases or related symptoms should have regular check-ups and discontinue use if necessary. Women planning to become pregnant or who could be pregnant should avoid this medication, as it can have a severe impact on the fetus during pregnancy and should never be taken. This medication can affect blood clotting, increasing the risk of bleeding if you are taking anticoagulants or blood-related medications; therefore, it should be used with caution after consulting a healthcare provider. The elderly may experience weakened renal, hepatic, and cardiac function; thus, they should take the minimal effective dose and carefully monitor for adverse reactions. During the use of this medication, there may be dizziness or drowsiness while driving or operating machinery, so caution is needed. Drug interactions may occur when used with other non-steroidal anti-inflammatory drugs or specific medications, so be sure to inform healthcare providers if you are taking any other medications. Regular blood tests and liver and kidney function tests are important if this medication is taken long-term. In case of overdose, gastrointestinal bleeding, renal and hepatic dysfunction, and severe intoxication symptoms may occur, so strict adherence to the prescribed dosage is necessary; in case of overdose, visit a hospital immediately. This medication should be kept out of the reach of children and stored sealed in its original container.

Gastrointestinal bleeding, major cardiovascular thrombotic events, myocardial infarction, stroke, bleeding from the stomach or intestines, ulcers, perforation, exfoliative dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis, anaphylactic reactions, interstitial nephritis, glomerulonephritis, renal medullary necrosis, nephrotic syndrome, increased serum transaminases, elevated liver function indices, increased plasma creatinine, elevated blood urea nitrogen, aplastic anemia, bone marrow suppression, changes in blood cell counts, leukopenia, thrombocytopenia, anemia, decreased plasma iron, reduced hemoglobin, decreased hematocrit, increased neutrophils, increased eosinophils, increased basophils, increased monocytes, agranulocytosis, anaphylaxis, anaphylactoid reactions, discomfort, confusion, loss of sense of direction, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, irritability, dizziness, drowsiness, headache, cranial pressure, fatigue, lethargy, taste dysfunction, mental clouding, seizures, sensory disturbances, tremors, blurred vision, conjunctivitis, foreign body sensation in the eye, bleeding of the sclera, tinnitus, palpitations, elevated blood pressure, flushing, arrhythmias, tachycardia, hypotension, hypertension, myocardial infarction, angina pectoris, heart failure, vasculitis, cough, upper respiratory infections, asthma, bronchospasm, difficulty breathing, allergic reactions to aspirin and other non-steroidal anti-inflammatory drugs, dyspepsia, nausea, vomiting, abdominal pain, constipation, bloating, diarrhea, loss of appetite, peptic ulcers, occult or overt gastrointestinal bleeding, stomatitis, gastritis, esophagitis, belching, dry mouth, thirst, cheilitis, occult blood in stool, 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 retention, elevated plasma creatinine level, increased urea level, decreased total protein, reduced albumin, proteinuria, glucosuria, increased urine sediment, hematuria, sodium and fluid retention, hyperkalemia, acute kidney failure, decreased urine output, frequent urination, urinary tract infections, interstitial nephritis, edema, lower extremity edema, malaise, fever, facial edema, syncope, weight loss, weight gain, pain in the axilla and breast, arthralgia, lumbago, pain in the axilla and chest, rigidity, lower limb weakness, diminished female reproductive capacity, dehydration, drowsiness, nausea, vomiting, epigastric pain, hypertension, acute renal failure, liver failure, respiratory depression, coma, seizures, cardiovascular collapse, cardiac arrest

This medication may be sensitive to light, so it should be stored in light-protective containers. Additionally, the medication should be stored in a safe temperature range of 1 to 30 degrees Celsius, avoiding extremely hot or cold environments.

Appearance

Yellow powder, hard capsule with light green (top) - light green (bottom)

Package unit

30 capsules/bottle, 300 capsules/bottle