Melzibic Capsule 7.5 mg (Meloxicam)

Adult dose

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 15 mg per day as needed. Rheumatoid arthritis, ankylosing spondylitis: ○ Adults: Administer 15 mg of this medicine orally once daily. The dose may be reduced to 7.5 mg per day depending on 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 initiated at a dose of 7.5 mg per day. ○ Patients with severe renal failure receiving hemodialysis should not receive more than 7.5 mg per day.

This medication can cause gastrointestinal bleeding if taken by individuals who regularly consume more than three drinks a day, so consultation with a doctor or pharmacist is mandatory. This medication may increase the risk of cardiovascular disease, so individuals with heart or vascular diseases or risk factors should closely monitor symptoms during use. This medication may increase the risk of serious issues such as gastrointestinal bleeding, ulcers, and perforations, so individuals with a history of gastrointestinal diseases or the elderly should be especially cautious. Severe allergic reactions or dermatitis may occur; if any skin abnormalities develop, discontinue use immediately and consult a doctor. This medication may affect kidney and liver function; individuals with kidney or liver diseases or compromised function should consult a specialist before use. Women planning a pregnancy or who may be pregnant should avoid this medication, as it can affect fertility. This medication should not be used by individuals with certain genetic lactose intolerance, and those with a history of allergies should be cautious. During treatment, regular blood tests and liver and kidney function tests are necessary to detect and manage abnormalities early. Use with other medications may interact, increasing the risk of bleeding or altering efficacy, so patients should inform their doctor of any medications they are taking. This medication is particularly to be avoided during pregnancy and should also not be used while breastfeeding. Elderly patients may experience more severe adverse reactions due to weakened body function, so treatment should begin with the minimum dosage. In case of overdose, symptoms may include drowsiness, nausea, vomiting, and in severe cases, can lead to renal failure or heart problems, necessitating immediate medical attention. This medication should be kept out of reach of children and stored in its original container to maintain quality.

Gastrointestinal bleeding, serious cardiovascular thrombotic reactions, 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, serum transaminase elevation, liver function test elevation, plasma creatinine increase, blood urea nitrogen increase, aplastic anemia, bone marrow suppression, change in blood cell count, leukopenia, thrombocytopenia, anemia, decreased plasma iron, decreased hemoglobin, decreased hematocrit levels, neutrophilia, eosinophilia, basophilia, monocytosis, agranulocytosis, anaphylaxis, anaphylactoid reactions, discomfort, confusion, loss of orientation, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, nervousness, dizziness, drowsiness, headache, intracranial pressure, 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, heart failure, vasculitis, cough, upper respiratory infection, asthma, bronchospasm, dyspnea, dyspepsia, nausea, vomiting, abdominal pain, constipation, distension, diarrhea, anorexia, peptic ulcer, occult gastrointestinal bleeding, visible 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, bilirubin elevation, jaundice, liver failure, alopecia, increased sweating, skin rash, urticaria, itching, angioedema, vesicular dermatitis, erythema multiforme, photosensitivity reactions, contact dermatitis, fixed drug eruption, urination disorders, elevated plasma creatinine levels, increased urea levels, decreased total protein, decreased albumin, proteinuria, glucosuria, increased urine sediment, hematuria, sodium retention, fluid retention, hyperkalemia, acute renal failure, decreased urine output, frequent urination, urinary tract infection, interstitial nephritis, edema, peripheral edema, malaise, fever, facial edema, syncope, weight loss, weight gain, axillary pain, breast pain, arthralgia, back pain, chest pain, stiffness, lower limb weakness, decreased 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 is sensitive to light, so it should be stored in a closed container that blocks light. Additionally, it is important to store it at room temperature between 1 to 30 degrees Celsius to maintain its efficacy.

Appearance

A capsule with yellowish powder contained, upper green capsule

Package unit

30 capsules/bottle, 100 capsules/bottle