Melocan Capsule (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 per day as needed. Rheumatoid arthritis, ankylosing spondylitis: Adults: Administer this medicine 15 mg orally once daily. The dose may be reduced to 7.5 mg per day according to response to treatment. Do not administer more than 15 mg per day. Take 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 impairment receiving hemodialysis must not receive more than 7.5 mg per day.

People who regularly consume three or more alcoholic beverages daily should consult a doctor or pharmacist before taking this medication. This is because the use of this drug may cause gastrointestinal bleeding. This drug may impact the cardiovascular system and increase the risk of serious cardiovascular diseases such as myocardial infarction or stroke. Particularly, those with a history of cardiovascular disease or risk factors should exercise additional caution and discontinue use immediately if symptoms such as chest pain or shortness of breath occur. This drug can cause serious gastrointestinal side effects such as gastrointestinal bleeding, ulcers, and perforations. Elders or those with a history of gastrointestinal disease should be particularly careful, and if symptoms of gastrointestinal bleeding are suspected, immediate treatment should be sought. This medicine can cause serious skin reactions or life-threatening hypersensitivity reactions, so if symptoms such as skin rashes or mucosal damage occur, discontinue use immediately. This drug may affect kidney function and can also cause liver dysfunction, so those with liver or kidney disease should undergo regular tests. This medication should not be used by women who are pregnant or planning to become pregnant, and breastfeeding women should also avoid its use. This is because this drug can harm the fetus or newborn. When used with other non-steroidal anti-inflammatory drugs or specific medications, the risk of side effects may increase, so anyone taking other medications should consult their doctor. For elderly patients, since liver, kidney, and heart functions may be weakened, it should be administered at the minimum dosage with careful consideration, especially regarding adverse reaction occurrences. In case of overdose, symptoms like drowsiness, nausea, vomiting, and gastrointestinal bleeding may occur, so if an overdose is suspected, immediate medical attention should be sought for appropriate treatment. This medication must be stored out of the reach of children and kept in its original container to prevent degradation of quality or misuse.

Gastrointestinal bleeding, serious cardiovascular thrombotic reactions, 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, serum transaminase elevation, liver function test elevation, plasma creatinine increase, blood urea nitrogen increase, aplastic anemia, bone marrow suppression, changes in blood cell counts, leukopenia, thrombocytopenia, anemia, decreased plasma iron, hemoglobin reduction, decreased hematocrit, neutrophilia, eosinophilia, basophilia, monocytosis, agranulocytosis, anaphylaxis, anaphylactic-like reactions, malaise, confusion, loss of orientation, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, nervousness, dizziness, drowsiness, headache, cranial pain, fatigue, lethargy, taste dysfunction, mental confusion, convulsions, sensory abnormalities, tremors, blurred vision, visual impairment, conjunctivitis, foreign body sensation in the eye, tinnitus, palpitations, increased blood pressure, flushing, facial flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina pectoris, heart failure, vasculitis, cough, upper respiratory infection, asthma, bronchospasm, shortness of breath, indigestion, nausea, vomiting, abdominal pain, constipation, bloating, diarrhea, loss of appetite, peptic ulcers, occult gastrointestinal bleeding, gross gastrointestinal bleeding, stomatitis, gastritis, esophagitis, belching, dry mouth, thirst, angular cheilitis, occult blood in stools, gastric 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, elevated plasma creatinine levels, elevated urea levels, decreased total protein, decreased albumin, proteinuria, glucosuria, increased urine sediment, hematuria, sodium and water retention, hyperkalemia, acute renal failure, decreased urine output, frequent urination, urinary tract infection, interstitial nephritis, edema, peripheral edema, lethargy, fever, facial edema, syncope, weight loss, weight gain, axillary and breast pain, arthralgia, low back pain, axillary and 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, convulsions, cardiac vascular collapse, cardiac arrest

This medication is sensitive to light, so it should be stored in a container that does not allow light to pass through. Additionally, it is important to store the medication at room temperature between 1°C and 30°C. Proper storage allows the drug's effectiveness to be maintained for a longer period.

Appearance

Hard capsule with a greenish color filled with yellow powder

Package unit

30 capsules/bottle, 300 capsules/bottle