Melix Capsule (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 once 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 once daily 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. ○ In elderly patients or those at increased risk of adverse reactions, treatment is usually started at a dose of 7.5 mg once daily. ○ Patients with severe renal impairment receiving hemodialysis should not receive more than 7.5 mg per day.

This medication may cause gastrointestinal bleeding if taken by individuals who regularly consume more than three alcoholic drinks daily; therefore, it is essential to consult with a doctor or pharmacist. This medication can increase the risk of cardiovascular diseases such as myocardial infarction or stroke for individuals with heart or vascular issues or risk factors, so cardiovascular symptoms must be carefully monitored during treatment. It may cause serious issues such as gastrointestinal bleeding, ulcers, or perforations, particularly in the elderly or individuals with a history of gastrointestinal diseases, who should be especially cautious. This medication may cause serious allergic reactions or hypersensitivity, so if symptoms such as skin rash or mucosal damage occur, it should be immediately discontinued. It may affect kidney function, so patients with kidney disease or decreased renal function should periodically monitor their kidney function while taking this medication. Liver function abnormalities may occur; if there is a history of liver disease or abnormalities are found in liver function tests, the use of this medication should be discontinued, and the doctor should be consulted. This medication should not be taken by women who are pregnant or planning to become pregnant, as it may reduce reproductive capacity, and women planning pregnancy should avoid it. This medication should not be administered to patients with certain genetic metabolic disorders, and individuals allergic to aspirin or other non-steroidal anti-inflammatory drugs should also refrain from taking it. During treatment, caution should be exercised while driving or operating machinery as dizziness, drowsiness, or blurred vision may occur. This medication may interact with other drugs, so it is important to discuss with a doctor if taking anticoagulants, diuretics, lithium, methotrexate, etc. When taking this medication, it is advisable to use the smallest effective dose for the shortest duration possible, and long-term use may require regular blood tests and assessments of liver and kidney function. Excessive intake of this medication may result in serious side effects, so the dosage should be adhered to, and immediate medical attention should be sought in the event of overdose. When storing, keep out of reach of children, and seal and store in the original container.

Gastrointestinal hemorrhage, cardiovascular thromboembolic events, myocardial infarction, stroke, bleeding from the stomach or intestines, ulcer, perforation, exfoliative dermatitis, mucocutaneous syndrome, toxic epidermal necrolysis, anaphylactic reaction, 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, increased neutrophils, increased eosinophils, increased basophils, increased monocytes, agranulocytosis, anaphylaxis, anaphylactoid reaction, malaise, confusion, disorientation, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, irritability, dizziness, drowsiness, headache, head pain, fatigue, languor, taste dysfunction, mental confusion, seizures, sensory disturbances, tremor, blurred vision, visual impairment, conjunctivitis, sensation of foreign body in the eye, scleral hemorrhage, tinnitus, palpitations, elevated blood pressure, flushing, facial flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina pectoris, heart failure, vasculitis, cough, upper respiratory tract infection, asthma, bronchospasm, dyspnea, allergic reactions to aspirin and other nonsteroidal anti-inflammatory drugs, dyspepsia, nausea, vomiting, abdominal pain, constipation, bloating, diarrhea, anorexia, peptic ulcer, occult gastrointestinal bleeding, macroscopic gastrointestinal bleeding, stomatitis, gastritis, esophagitis, belching, dry mouth, thirst, angular cheilitis, occult blood in stool, gastric perforation, colitis, pancreatitis, melena, perforated peptic ulcer, hepatitis, elevated plasma transaminase levels, increased bilirubin, jaundice, hepatic failure, skin rash, urticaria, pruritus, angioedema, vesicular dermatitis, erythema multiforme, photosensitivity reaction, contact dermatitis, fixed drug eruption, urinary retention, elevated plasma creatinine levels, increased urea, decreased total protein, reduced albumin, proteinuria, glucosuria, increased urinary sediment, hematuria, sodium and fluid retention, hyperkalemia, acute renal failure, decreased urine output, frequency of urination, urinary tract infection, interstitial nephritis, edema, lower extremity edema, lethargy, fever, facial edema, syncope, weight loss, weight gain, axillary or breast pain, arthralgia, low back pain, axillary or chest pain, rigidity, weakness in the lower limbs, decreased reproductive ability in women, dehydration, drowsiness, nausea, vomiting, epigastric pain, hypertension, acute renal failure, hepatic failure, respiratory depression, coma, seizures, cardiovascular collapse, cardiac arrest

This medication is sensitive to light and should be stored in a special container that blocks light. Moreover, it should be stored at temperatures between 1 degree and 30 degrees Celsius to maintain effectiveness.

Appearance

Hard capsules with yellow or light yellow powder, greenish blue on the top and bottom.

Package unit

30 capsules/bottle, 100 capsules/bottle