Viewing nowMelosid Capsule 7.5 mg (Meloxicam)
Meloxicam 7.5mg
Hard capsule · Prescription medication
Jeil Pharmaceutical Co., Ltd.

MFDS item code 201308010 · Approved 2013.07.04 · Insurance code 645404010
Short-term treatment of symptoms during acute exacerbations of osteoarthritis; symptomatic treatment of rheumatoid arthritis and ankylosing spondylitis
This medication is used to treat symptoms of arthritis such as osteoarthritis, rheumatoid arthritis, and ankylosing spondylitis. It especially helps alleviate pain and movement disorders, reducing discomfort caused by inflammation to help patients live more comfortably in their daily lives. It is effective for rapid symptom improvement during acute exacerbations and aids in the restoration of joint function through ongoing treatment. Overall, it is used to relieve pain and stiffness caused by arthritis to improve quality of life.
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 15 mg 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 daily according to the response to treatment. Do not administer more than 15 mg of this drug daily. 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 daily. ○ Patients with severe renal impairment receiving hemodialysis should not receive more than 7.5 mg daily.
This medication may cause serious side effects such as gastrointestinal bleeding if taken by individuals who regularly consume more than three glasses of alcohol daily, so consultation with a doctor or pharmacist is essential. This medication may increase the risk of cardiovascular diseases, so caution is particularly required for those with a history of heart disease or stroke or risk factors. If symptoms such as chest pain, shortness of breath, weakness, or slurred speech occur while taking this medication, it should be discontinued immediately, and medical advice should be sought. This medication can cause serious gastrointestinal issues such as gastrointestinal bleeding, ulcers, and perforations; thus, individuals with a history of gastrointestinal diseases or elderly individuals should exercise greater caution. Severe allergic reactions or rashes may occur on the skin, so if such symptoms appear, it should be discontinued immediately. It may affect kidney and liver function, so those with kidney or liver diseases or related symptoms should consult medical personnel. Women who are pregnant or planning to become pregnant should not take this medication, as it may affect reproductive ability. This medication is not administered to individuals with certain genetic problems and should be avoided by those with hypersensitivity or allergies to aspirin or other non-steroidal anti-inflammatory drugs.</s> Patients with specific diseases such as hypertension, heart failure, kidney disease, or blood disorders should use this medication with caution and require regular examinations and monitoring. There is an increased risk of bleeding or renal toxicity when taken in conjunction with other medications, so it is essential to inform a doctor of any other medications being taken. This medication may cause drowsiness, dizziness, or visual disturbances, so caution is necessary when driving or operating machinery. In case of overdose, symptoms such as vomiting, gastrointestinal bleeding, and in severe cases, kidney failure or heart problems may occur, and immediate medical attention should be sought. This medication should be kept out of reach of children and stored in its original container to maintain its quality.
Gastrointestinal bleeding, cardiovascular thromboembolic events, myocardial infarction, stroke, stomach or intestinal bleeding, ulcer, perforation, exfoliative dermatitis, mucocutaneous syndrome, toxic epidermal necrolysis, anaphylactic reaction, interstitial nephritis, glomerulonephritis, renal medullary necrosis, nephrotic syndrome, elevated serum transaminase levels, 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, decreased hemoglobin, reduced hematocrit, neutrophilia, eosinophilia, basophilia, monocytosis, agranulocytosis, anaphylaxis, anaphylactoid reaction, malaise, confusion, loss of orientation, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, irritability, dizziness, drowsiness, headache, migraine, fatigue, lethargy, taste dysfunction, mental disorientation, seizures, sensory disturbances, tremors, blurred vision, conjunctivitis, foreign body sensation in the eye, subconjunctival hemorrhage, tinnitus, palpitations, increased 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 non-steroidal anti-inflammatory drugs, dyspepsia, nausea, vomiting, abdominal pain, constipation, bloating, diarrhea, decreased appetite, peptic ulcer, occult gastrointestinal bleeding, gross gastrointestinal bleeding, stomatitis, gastritis, esophagitis, belching, dry mouth, thirst, angular cheilitis, fecal occult blood, gastric perforation, colitis, pancreatitis, melena, perforated peptic ulcer, hepatitis, elevated plasma transaminase concentration, increased bilirubin, jaundice, liver failure, skin rash, urticaria, itching, angioedema, vesicular dermatitis, erythema multiforme, phototoxic reactions, contact dermatitis, fixed drug eruption, urinary retention, elevated plasma creatinine levels, increased urea levels, proteinuria, glycosuria, increased urinary sediment, urinary hematuria, sodium and fluid retention, hyperkalemia, acute renal failure, decreased urine output, frequency of urination, urinary tract infection, interstitial nephritis, edema, lower limb edema, fatigue, 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, seizures, cardiovascular collapse, cardiac arrest
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a sealed container that blocks light and kept at room temperature between 1 to 30 degrees Celsius. Storing it this way helps maintain the medication's efficacy and prevents deterioration.
A hard capsule containing a pale yellow powder, with a dark green upper and lower part.
30 capsules/bottle, 100 capsules/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.