Molexel Capsule 7.5 mg (Meloxicam)

Adult dose

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. Rheumatoid arthritis, ankylosing spondylitis: ○ Adults: Administer 15 mg of meloxicam 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 medicine daily. Take the daily dose all at once with water or another beverage during a meal. ○ For 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 impairment receiving hemodialysis should not receive more than 7.5 mg daily.

Patients who regularly consume more than three alcoholic beverages a day should consult with their doctor or pharmacist before taking this medication, as it may cause gastrointestinal bleeding. This medication may affect the cardiovascular system and increase the risk of serious thrombotic reactions such as heart attack or stroke. Caution is especially necessary for individuals with cardiovascular diseases or risk factors, and they should discontinue use immediately if symptoms such as chest pain or shortness of breath occur. This medication can cause serious gastrointestinal issues such as bleeding, ulcers, or perforations. These side effects may be more severe in the elderly and in patients with a history of gastrointestinal disorders or those on anticoagulants. Rarely, serious allergic reactions or skin conditions, such as dermatitis or life-threatening hypersensitivity reactions like anaphylaxis, may occur. If skin rashes or mucosal damage occur, patients should stop taking the medication immediately. This medication can impact kidney function; hence, individuals with renal diseases or impaired kidney function should use it cautiously. Attention is also required for patients with liver dysfunction or liver disease. Women should avoid this medication if planning to conceive, as it may decrease fertility. Pregnant or nursing women should also avoid taking this medication. This medication should not be administered to individuals with specific genetic issues (e.g., galactose intolerance), known allergies to its components, or hypersensitivity to aspirin or other non-steroidal anti-inflammatory drugs. Elderly patients or those with existing diseases such as gastrointestinal disorders, cardiovascular diseases, or renal diseases should take this medication more cautiously. Adverse effects such as drowsiness or dizziness may occur when driving or operating machinery. This medication may interact with other drugs; therefore, patients should consult their physician and undergo regular examinations, especially when taking anticoagulants, diuretics, lithium, or methotrexate. In case of overdose, nausea, vomiting, gastrointestinal bleeding, and in severe cases acute renal failure or liver failure, as well as loss of consciousness may occur, hence immediate medical attention is required. There is no antidote, so gastric lavage and supportive treatment are necessary. Store this medication out of reach of children, in its original sealed container to maintain quality.

Gastrointestinal bleeding, serious cardiovascular thrombotic reactions, myocardial infarction, stroke, bleeding of the stomach or intestines, ulcers, perforations, exfoliative dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis, anaphylaxis, interstitial nephritis, glomerulonephritis, nephrotoxicity, 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, leukopenia, thrombocytopenia, anemia, decreased plasma iron, decreased hemoglobin, decreased hematocrit, neutrophilia, eosinophilia, basophilia, monocytosis, agranulocytosis, anaphylaxis, anaphylactoid reactions, discomfort, confusion, loss of orientation, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, irritability, dizziness, drowsiness, headache, vertex heaviness, fatigue, lethargy, taste dysfunction, mental confusion, seizures, sensory disturbances, tremors, blurred vision, conjunctivitis, foreign body sensation in the eye, scleral hemorrhage, tinnitus, palpitations, increased blood pressure, flushing, facial flushing, arrhythmias, tachycardia, hypotension, hypertension, myocardial infarction, angina pectoris, heart failure, vasculitis, cough, upper respiratory infection, asthma, bronchospasm, dyspnea, allergic reactions to aspirin and other non-steroidal anti-inflammatory drugs, 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, cheilitis, occult blood in stool, gastrointestinal perforation, colitis, pancreatitis, melena, perforated peptic ulcer, hepatitis, elevated plasma transaminase levels, elevated bilirubin, jaundice, liver failure, alopecia, increased sweating, skin rash, urticaria, itching, angioedema, vesicular dermatitis, erythema multiforme, photosensitivity reactions, contact dermatitis, fixed drug eruption, urine retention, elevated plasma creatinine levels, increased urea levels, decreased total protein, decreased albumin, proteinuria, glycosuria, increased urinary sediment, hematuria, sodium and water retention, hyperkalemia, acute renal failure, decreased urine output, pollakiuria, urinary tract infection, interstitial nephritis, edema, peripheral edema, malaise, fever, facial edema, syncope, weight loss, weight gain, axillary breast pain, arthralgia, low back pain, axillary chest pain, rigidity, lower limb weakness, female reproductive capacity decrease, dehydration

This medication is sensitive to light and should be stored in an opaque container, at a temperature between 1 and 30 degrees Celsius. Maintaining the proper storage temperature ensures the medication's effectiveness.

Appearance

Yellow powder-filled bright green capsule

Package unit

30 capsules/bottle, 300 capsules/bottle