Meloxicam Capsule 7.5 mg (Meloxicam)

Adult dose

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 medicine 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 medicine daily. Take it with water or another beverage during a meal. ○ In older adults or patients at increased risk of adverse reactions, treatment is usually initiated at a dose of 7.5 mg daily. ○ Patients with severe renal failure receiving hemodialysis should not receive more than 7.5 mg daily.

This medication should be used with caution in those who regularly consume more than three alcoholic beverages a day, as it may increase the risk of gastrointestinal bleeding; thus it is essential to consult a doctor or pharmacist. As it contains non-steroidal anti-inflammatory drugs, it may cause cardiovascular issues, so those with heart disease or risk factors should be particularly careful. If symptoms such as chest pain, shortness of breath, or slurred speech occur while taking the medication, it should be discontinued immediately. Serious conditions such as gastrointestinal bleeding, ulcers, or perforation may occur, so caution is advised for those with a history of gastrointestinal disease or the elderly. Serious skin reactions like rashes or mucosal damage may appear, and if any abnormal symptoms occur, discontinue use immediately. This medication can affect kidney function, so those with kidney disease or taking diuretics, blood pressure medications, etc., should use it cautiously. Women who are pregnant or planning to become pregnant should not take this medication, nor should those who are breastfeeding. This medication should not be administered to individuals with certain genetic diseases and is contraindicated for those with allergies or hypersensitivity reactions. Long-term use requires regular blood tests and liver and kidney function tests, and any abnormal symptoms should be reported to a doctor immediately. The risk of bleeding or reduced kidney function may increase when used in conjunction with other medications, so it is imperative to inform healthcare providers of any other medications being taken. Drowsiness or dizziness may occur when driving or operating machinery, so caution is necessary. The dosage and duration of treatment should be kept to a minimum, and dosages should not be increased arbitrarily if symptoms do not improve. Serious side effects may occur with overdose, so the prescribed dosage should be strictly followed, and if an overdose occurs, seek medical attention immediately. Keep out of reach of children and store in the original container, tightly closed.

Gastrointestinal bleeding, cardiovascular thromboembolic 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, 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 levels, neutrophilia, eosinophilia, basophilia, monocytosis, agranulocytosis, anaphylaxis, anaphylactoid reactions, discomfort, confusion, loss of directional sense, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, irritability, dizziness, drowsiness, headache, cranial pressure, fatigue, lethargy, taste disorders, mental confusion, seizures, sensory disturbances, tremors, blurred vision, conjunctivitis, foreign body sensation in the eye, tinnitus, palpitations, increased blood pressure, flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina, heart failure, vasculitis, cough, upper respiratory tract infection, asthma, bronchial spasms, dyspnea, dyspepsia, nausea, vomiting, abdominal pain, constipation, bloating, diarrhea, loss of appetite, peptic ulcers, occult or overt gastrointestinal bleeding, stomatitis, gastritis, esophagitis, belching, dry mouth, thirst, angular cheilitis, occult blood in stool, gastrointestinal perforation, colitis, pancreatitis, melena, perforated peptic ulcer, hepatitis, elevated plasma transaminase levels, increased bilirubin, jaundice, liver failure, alopecia, increased sweating, skin rash, urticaria, pruritus, angioedema, vesicular dermatitis, erythema multiforme, photosensitivity reactions, contact dermatitis, fixed drug eruption, urinary disorders, 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, polyuria, urinary tract infections, interstitial nephritis, edema, peripheral edema, malaise, fever, facial swelling, syncope, weight loss, weight gain, pain in the armpit/breast, arthralgia, low back pain, pain in the armpit/chest, stiffness, weakness in the lower limbs, reduced female reproductive capacity, dehydration

This medication is sensitive to light and should be stored in a container that blocks light. It should also be stored at room temperature between 1 and 30 degrees Celsius. This helps maintain the medication's effectiveness and safety.

Appearance

A hard capsule with a green upper and lower part filled with a light yellow content

Package unit

30 capsules/bottle, 300 capsules/bottle, 500 capsules/bottle