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

MFDS item code 200502090 · Notified 2005.10.18 · Insurance code 657800630
Relief of symptoms of rheumatoid arthritis, acute exacerbations of osteoarthritis, and ankylosing spondylitis
This medication is primarily used to relieve symptoms such as pain and motor coordination issues during acute exacerbations of osteoarthritis in a short period of time. It also effectively treats symptoms of rheumatoid arthritis and ankylosing spondylitis. In other words, it helps improve various inflammation and pain related to arthritis. This medication can reduce inflammation and discomfort in the joints, contributing to an improved quality of life for patients. Overall, this medication is used for treating various types of arthritis symptoms.
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 depending on the response to treatment. Do not administer more than 15 mg of this drug per day. Take it with water or another beverage during a meal. ○ For 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 undergoing hemodialysis should not receive more than 7.5 mg daily.
This medication must be consulted with a physician or pharmacist before use by those who regularly consume more than three glasses of alcohol daily. This is because this medication can cause gastrointestinal bleeding. This medication can affect the cardiovascular system and may increase the risk of serious thrombotic events such as heart attack or stroke. Those with cardiovascular disease or risk factors should be especially cautious and stop taking the medication immediately if symptoms such as chest pain or shortness of breath occur. This medication may elevate the risk of serious gastrointestinal problems such as bleeding, ulcers, or perforations. Such gastrointestinal issues may manifest more severely in older individuals, and those with a history of gastrointestinal disease or those on anticoagulants should use it more cautiously. This medication can lead to severe skin reactions or allergic reactions, so if symptoms such as skin rashes or mucosal damage occur, you must stop taking it immediately and seek medical attention. As it can affect kidney and liver function, individuals with kidney or liver issues should consult with a physician before use and require regular check-ups during treatment. This medication may decrease fertility, so it is advised that women planning to become pregnant avoid this medication, and women who are pregnant or breastfeeding should not use it. This medication cannot be administered to individuals who cannot break down lactose due to specific genetic problems. Before taking this medication, inform your physician if you have had allergic reactions to this or similar medications, or if you have a history of gastrointestinal bleeding or ulcers. Elderly individuals or those with a history of gastrointestinal disease, and those at risk for cardiovascular disease should use this medication cautiously, as drowsiness or dizziness may occur during driving or operating machinery. Regular blood tests and liver and kidney function tests should be performed during treatment, and if any unusual symptoms occur, consult your physician immediately. There may be interactions with other medications; therefore, inform your physician or pharmacist if you are currently taking other medications. In the case of overdose, symptoms such as nausea, vomiting, and gastrointestinal bleeding may occur, and immediate medical treatment should be sought. Store this medication out of the reach of children and keep it sealed in its original container.
Gastrointestinal bleeding, serious cardiovascular thrombotic reaction, myocardial infarction, stroke, bleeding of the stomach or intestines, ulcers, perforation, exfoliative dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis, anaphylactic reaction, interstitial nephritis, glomerulonephritis, renal medullary necrosis, nephrotic syndrome, serum transaminase elevation, increased liver function tests, increased 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, loss of directional sense, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, nervousness, dizziness, drowsiness, headache, head heaviness, fatigue, lethargy, taste dysfunction, mental confusion, convulsions, sensory disturbances, tremor, blurred vision, conjunctivitis, foreign body sensation 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 infection, asthma, bronchospasm, shortness of breath, dyspepsia, nausea, vomiting, abdominal pain, constipation, bloating, diarrhea, loss of appetite, peptic ulcer, occult gastrointestinal bleeding, overt gastrointestinal bleeding, stomatitis, gastritis, esophagitis, belching, dry mouth, thirst, angular cheilitis, occult blood in urine, gastric perforation, colitis, pancreatitis, melena, perforated 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 reaction, contact dermatitis, fixed drug eruption, urinary disorders, elevated plasma creatinine levels, increased urea levels, decreased total protein, decreased albumin, proteinuria, glucosuria, increased urinary sediment, hematuria, sodium and fluid retention, hyperkalemia, acute renal failure, decreased urine output, frequent urination, urinary tract infection, interstitial nephritis, edema, peripheral edema, malaise, fever, facial swelling, syncope, weight loss, weight gain, axillary and breast pain, arthralgia, low back pain, axillary and chest pain, rigidity, lower limb weakness, decreased female reproductive capacity, dehydration
Not everyone experiences these, and they can vary from person to person.
This medication may be sensitive to light, so it should be stored in a container that blocks light. Additionally, it is best to store the medication at a temperature between 1 degree and 30 degrees Celsius at room temperature to maintain its effectiveness and safety.
Hard capsule filled with a light yellow granule, upper and lower parts in dark green.
30 capsules/bottle, 300 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.