Daiwoong Biotech Meloxicam Capsule 15mg

Adult dose

1. 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 up to 15 mg once daily as needed. 2. Rheumatoid arthritis, ankylosing spondylitis: ○ Adults: Administer 15 mg of this drug 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 drug per day. Take with water or another beverage during a meal. ○ In older adults or individuals at increased risk of adverse reactions, treatment is usually initiated at a dose of 7.5 mg once daily. ○ Patients with severe renal failure receiving hemodialysis should not receive more than 7.5 mg per day.

This medication should be discussed with a physician or pharmacist before use by those who regularly consume three or more alcoholic beverages a day. This medication may cause gastrointestinal bleeding, so caution is needed. It can increase the risk of cardiovascular disease; therefore, patients with a history of heart disease or risk factors should use it more cautiously. If symptoms such as chest pain, shortness of breath, weakness, or stuttering occur, discontinue the medication immediately. Serious adverse reactions related to the gastrointestinal tract, such as gastrointestinal bleeding, ulcers, or perforation, may occur, particularly in elderly patients or those with a history of gastrointestinal disease. Severe allergic reactions on the skin or severe rashes may occur, and if such symptoms appear, the medication should be discontinued. It may affect kidney function, and patients with kidney disease, hypertension, or heart failure require regular kidney function tests. Women who are pregnant or may become pregnant should not use this medication, as it may affect reproductive ability, and women planning to become pregnant should also avoid taking it. This medication should not be administered to certain genetic lactose intolerant patients. There are many drug interactions, so inform your physician or pharmacist of any current medications you are taking. For long-term use, regular blood tests, liver function tests, and kidney function tests are necessary, and if abnormal symptoms are present, consult healthcare professionals immediately. This medication is not to be administered to children, especially adolescents under 15 years of age. Caution is necessary when driving or operating machinery, as symptoms such as dizziness or drowsiness may occur. In case of overdose, symptoms such as nausea, vomiting, gastrointestinal bleeding, and severe cases may lead to kidney failure or heart problems, necessitating immediate emergency treatment. Store this medication out of reach of children and keep it in its original container.

Gastrointestinal bleeding, severe cardiovascular thrombotic reactions, myocardial infarction, stroke, bleeding from the stomach or intestines, ulceration, 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 tests, increased plasma creatinine, elevated blood urea nitrogen, aplastic anemia, bone marrow suppression, changes in blood cell counts, leukopenia, thrombocytopenia, anemia, decreased plasma iron, decreased hemoglobin, reduced hematocrit, increased neutrophils, increased eosinophils, increased basophils, increased monocytes, agranulocytosis, anaphylaxis, anaphylactoid reactions, malaise, confusion, disorientation, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, irritability, dizziness, drowsiness, headache, cranial pressure, fatigue, lethargy, taste dysfunction, mental confusion, seizures, sensory disturbances, tremors, visual blurriness, vision impairment, conjunctivitis, foreign body sensation in the eye, subconjunctival hemorrhage, tinnitus, palpitations, increased blood pressure, flushing, facial flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina, heart failure, vasculitis, cough, upper respiratory tract 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 urine, gastric perforation, colitis, pancreatitis, melena, perforating peptic ulcer, hepatitis, elevated plasma transaminase levels, increased bilirubin, jaundice, liver failure, alopecia, increased sweating, skin rash, urticaria, itching, angioedema, vesicular dermatitis, erythema multiforme, photosensitivity reactions, contact dermatitis, fixed drug eruption, urinary disturbances, elevated plasma creatinine levels, increased urea, decreased total protein, decreased 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 limb edema, malaise, fever, facial edema, syncope, weight loss, weight gain, axillary and breast pain, arthralgia, low back pain, axillary and chest pain, rigidity, lower limb weakness, reduced female reproductive capacity, dehydration

This medication should be stored in a tightly closed container that blocks light and kept at a temperature between 1 to 30 degrees Celsius. Storing it properly will maintain the drug's efficacy and prevent deterioration.

Appearance

Greenish upper part and yellow lower part capsule containing a pale yellow powder

Package unit

30 capsules/bottle, 300 capsules/bottle