Viewing nowMeloxicam Capsule 7.5 mg (Meloxicam)
Meloxicam 7.5mg
Hard capsule · Prescription medication
Light Pharm Tech Co., Ltd.

MFDS item code 201908115 · Approved 2019.11.27 · Insurance code 690302080
Relief of symptoms of rheumatoid arthritis, acute exacerbations of osteoarthritis, and ankylosing spondylitis
This medication is used for short-term symptomatic treatment during acute exacerbations of osteoarthritis accompanied by pain and motor impairment. It is also effective in relieving symptoms of rheumatoid arthritis and ankylosing spondylitis. Therefore, it helps reduce discomfort due to arthritis and aids in daily activities.
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 to 15 mg daily as needed. 2. Rheumatoid arthritis and ankylosing spondylitis: ○ Adults: Administer this drug 15 mg 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 per day. Take it with water or another beverage during a meal. ○ In older adults or patients at increased risk of adverse reactions, treatment is generally started 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 gastrointestinal bleeding if taken by individuals who regularly consume more than three drinks a day, so it should be discussed with a doctor or pharmacist. This medication may affect the cardiovascular system, potentially increasing the risk of serious cardiovascular diseases such as myocardial infarction or stroke, so those with a history of cardiovascular disease or risk factors should be cautious when taking it. If symptoms such as chest pain, shortness of breath, weakness, or slurred speech occur during use, discontinue the medication immediately and consult a healthcare professional. This medication can burden the stomach and pose a risk of serious problems such as bleeding, ulcers, or perforation in the stomach or intestines. Particularly, the elderly or those with a history of gastrointestinal disease should be more vigilant regarding these gastrointestinal-related side effects, and if symptoms like gastrointestinal bleeding or pain appear during use, immediate evaluation and treatment are necessary. This medication can cause severe allergic reactions or serious dermatitis, so if symptoms such as skin rashes or mucosal damage occur, discontinue use. It may affect kidney function, and individuals with kidney disease or those taking diuretics should regularly monitor kidney function. Women who are planning to become pregnant or may be pregnant should not take this medication, and it should absolutely not be used during pregnancy as it may harm the fetus. Breastfeeding women should also avoid this medication, and the elderly, who may have reduced kidney and liver functions, should take it cautiously at the minimum dosage. Before taking this medication, it is essential to inform your healthcare provider if you have had allergic reactions to this medication or similar medications, or if you have a history of asthma or gastrointestinal bleeding. Due to many drug interactions, especially if you are taking anticoagulants, diuretics, antihypertensives, lithium, or methotrexate, you should consult with a doctor before taking this medication. During use, drowsiness, dizziness, or visual disturbances may occur, so caution is advised while driving or operating machinery. In case of overdose, nausea, vomiting, drowsiness, and in severe cases, kidney failure or heart issues may occur; thus, the prescribed dosage should be strictly followed. Lastly, this medication should be kept out of the reach of children and stored safely in its original container.
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, elevated serum transaminases, increased liver function tests, increased plasma creatinine, increased blood urea nitrogen, aplastic anemia, bone marrow suppression, changes in blood cell counts, leukocytopenia, thrombocytopenia, anemia, decreased plasma iron, decreased hemoglobin, decreased hematocrit, increased neutrophils, increased eosinophils, increased basophils, increased monocytes, agranulocytosis, anaphylaxis, anaphylactoid reactions, discomfort, confusion, loss of directional sense, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, irritability, dizziness, drowsiness, headache, head pressure, fatigue, lethargy, taste dysfunction, mental confusion, seizures, sensory disturbances, tremors, blurred vision, conjunctivitis, foreign body sensation in the eye, hemorrhage in the eye's sclera, tinnitus, palpitations, elevated blood pressure, flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina, heart failure, vasculitis, cough, upper respiratory infection, asthma, bronchospasm, dyspnea, dyspepsia, nausea, vomiting, abdominal pain, constipation, bloating, diarrhea, loss of appetite, peptic ulcer, occult or gross gastrointestinal bleeding, stomatitis, gastritis, esophagitis, belching, dry mouth, thirst, angular cheilitis, occult blood in stool, gastric perforation, colitis, pancreatitis, melena, perforated peptic ulcer, hepatitis, jaundice, hepatic failure, alopecia, increased sweating, skin rash, urticaria, angioedema, vesicular dermatitis, erythema multiforme, photosensitive reactions, contact dermatitis, fixed drug eruption, urinary disorders, proteinuria, glycosuria, increased urine sediment, hematuria, sodium and fluid retention, hyperkalemia, acute renal failure, decreased urine output, frequency of urination, urinary tract infections, interstitial nephritis, edema, peripheral edema, malaise, fever, facial swelling, syncope, weight loss, weight gain, pain in axilla and breast, arthralgia, low back pain, pain in axilla and chest, stiffness, lower limb weakness, decreased female reproductive ability, dehydration
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly closed container that protects it from light and kept at a temperature between 1 degree and 30 degrees Celsius. Additionally, it should be used within 36 months from the date of manufacture to maintain its efficacy and safety.
A hard capsule with green upper and lower parts filled with light yellow contents
30 capsules/bottle, 500 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.