Meloxicam Capsule 15 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 per day 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 per day according to the response to treatment. Do not administer more than 15 mg of this medicine per day. Take it with water or another beverage during a meal. ○ In elderly patients or those at increased risk of adverse reactions, treatment is usually started at a dose of 7.5 mg per day. ○ Patients with severe renal failure receiving hemodialysis must not receive more than 7.5 mg per day.

This medication may cause gastric bleeding in individuals who regularly consume more than three alcoholic beverages a day, so consultation with a doctor or pharmacist is essential. This medication can affect the cardiovascular system, increasing the risk of serious issues such as myocardial infarction or stroke, hence individuals with cardiovascular diseases or risk factors should exercise extra caution. If symptoms such as chest pain, shortness of breath, or slurred speech occur, the use of this medication should be stopped immediately and medical attention sought. Gastric bleeding or severe issues such as ulcers or perforations may occur, so those with a history of gastric disease or elderly individuals should be particularly cautious. This medication may cause severe skin reactions or allergic reactions, so if symptoms such as rashes or mucosal damage occur, it should be discontinued immediately. It may affect liver and kidney function; thus, those with liver or kidney issues or related symptoms should consult healthcare professionals. This medication may reduce reproductive ability, so women planning to become pregnant are advised to avoid its use. Individuals allergic to aspirin or other NSAIDs, those with a history of gastric bleeding or ulcers, severe liver or kidney disease patients, and women who are pregnant or breastfeeding should not take this medication. During the use of this medication, caution is advised as dizziness or drowsiness may occur when driving or operating machinery. It can interact with other medications, so especially inform your doctor or pharmacist if taking anticoagulants, diuretics, lithium, methotrexate, etc. Regular blood tests and liver and kidney function tests should be performed before and during long-term use to monitor for any abnormalities. In the case of overdose, symptoms such as vomiting, drowsiness, and gastric bleeding may arise, and immediate medical attention is required. This medication should be kept out of the reach of children and stored tightly sealed in its original container.

Gastrointestinal bleeding, cardiovascular thrombotic reaction, myocardial infarction, stroke, bleeding from the stomach or intestine, ulcer, perforation, exfoliative dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis, anaphylactic reaction, interstitial nephritis, glomerulonephritis, renal medullary necrosis, nephrotic syndrome, serum transaminase elevation, liver function test elevation, plasma creatinine increase, blood urea nitrogen increase, aplastic anemia, bone marrow suppression, blood cell count changes, leukopenia, 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, nervousness, dizziness, drowsiness, headache, head pain, fatigue, lethargy, dysgeusia, mental confusion, seizures, sensory abnormalities, tremors, blurred vision, conjunctivitis, foreign body sensation in the eye, subconjunctival hemorrhage, tinnitus, palpitations, increased blood pressure, flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina, heart failure, vasculitis, cough, upper respiratory infection, asthma, bronchospasm, shortness of breath, dyspepsia, nausea, vomiting, abdominal pain, constipation, distension, diarrhea, loss of appetite, peptic ulcer, occult or visible 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, liver failure, alopecia, increased sweating, skin rash, urticaria, angioedema, vesicular dermatitis, erythema multiforme, photosensitivity reactions, contact dermatitis, fixed drug eruption, urinary retention, increased plasma creatinine levels, elevated urea levels, decreased total protein, decreased albumin, proteinuria, glucosuria, increased urinary sediment, hematuria, sodium and fluid retention, hyperkalemia, acute renal failure, decreased urine output, increased frequency of urination, urinary tract infection, interstitial nephritis, edema, lower limb edema, malaise, fever, facial swelling, syncope, weight loss, weight gain, pain in armpits and breasts, arthralgia, low back pain, pain in armpits and chest, 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

This medication is sensitive to light and should be stored in a container that does not allow light to enter. Additionally, it is safe to store at room temperature, maintaining a temperature between 1 to 30 degrees.

Appearance

A hard capsule with a pale green upper part and a yellow lower part containing a pale yellow powder.

Package unit

30 capsules/bottle