Mobirrokam Capsule 7.5mg (Meloxicam)

Adult dose

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, ankylosing spondylitis: ○ Adults: Administer 15 mg of this medicine orally once daily. The dose may be reduced to 7.5 mg daily according to 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 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 failure receiving hemodialysis should not receive more than 7.5 mg daily.

This medication may cause gastrointestinal bleeding if taken regularly by individuals who consume more than three drinks per day, so it is essential to consult with a physician or pharmacist. This medication can affect the cardiovascular system and increase the risk of severe cardiovascular diseases such as myocardial infarction and stroke. Individuals with a history of such diseases or risk factors should exercise caution, and if symptoms such as chest pain or shortness of breath occur, they should immediately discontinue use and seek medical advice. This medication can cause serious gastrointestinal side effects such as gastrointestinal bleeding, ulcers, and perforations. Special caution is required for the elderly or those with a history of gastrointestinal diseases, and if symptoms like abdominal pain or bloody stool occur during use, immediate medical consultation is necessary. This medication can cause severe allergic reactions on the skin, so if symptoms such as skin rashes or mucosal damage occur, it should be discontinued immediately and medical advice should be sought. It may affect kidney function, so regular kidney function testing is necessary if there is a history of kidney disease or if diuretics or antihypertensive medications are being used. Women who are planning to become pregnant or may become pregnant should not use this medication, and it should not be taken during pregnancy as it can have severe effects on the fetus. This medication can interact with various drugs, so if other medications are being taken, it is crucial to inform healthcare providers, particularly with anticoagulants, diuretics, lithium, methotrexate, etc. Elderly individuals may experience more severe adverse reactions due to reduced physical function, so it should be used carefully at the lowest effective dose. Overdose of this medication can lead to nausea, vomiting, gastrointestinal bleeding, and in severe cases, kidney failure or heart problems, so it is important not to exceed the prescribed dose, and immediate emergency treatment is required in case of overdose. This medication must be kept away from children's reach, and it should be stored in its original container to prevent misuse or quality deterioration.

Gastrointestinal bleeding, serious cardiovascular thrombotic reactions, myocardial infarction, stroke, bleeding from the stomach or intestine, ulcers, perforation, exfoliative dermatitis, mucosal skin syndrome, toxic epidermal necrolysis, anaphylactic reactions, interstitial nephritis, glomerulonephritis, 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 count, leukopenia, thrombocytopenia, anemia, decreased plasma iron, reduced hemoglobin, decreased hematocrit, increased neutrophils, increased eosinophils, increased basophils, increased monocytes, agranulocytosis, anaphylaxis, anaphylactoid reaction, discomfort, confusion, loss of orientation, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, neurogenic irritability, dizziness, drowsiness, headache, head pressure, fatigue, lethargy, dysgeusia, 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, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina pectoris, heart failure, vasculitis, cough, upper respiratory infection, asthma, bronchial spasm, dyspnea, dyspepsia, nausea, vomiting, abdominal pain, constipation, distension, diarrhea, loss of appetite, peptic ulcer, occult gastrointestinal bleeding, macroscopic 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 reactions, contact dermatitis, fixed drug eruption, urination disorders, elevated plasma creatinine levels, increased urea levels, decreased total protein, decreased albumin, proteinuria, glycosuria, increased urinary sediment, hematuria, sodium and fluid retention, hyperkalemia, acute renal failure, decreased urine output, frequency of urination, urinary tract infection, interstitial nephritis, edema, peripheral edema, malaise, fever, facial edema, syncope, weight loss, weight gain, pain in the armpit and breast, arthralgia, low back pain, pain in the armpit and chest, rigidity, lower limb weakness, decreased female reproductive capacity, dehydration, drowsiness, nausea, epigastric pain, hypertension, acute renal failure, liver failure, respiratory depression, coma, seizures, cardiovascular collapse, cardiac arrest

This medication should be stored in a tightly closed container that protects it from light, ideally at room temperature between 1 degree and 30 degrees Celsius. Storing it this way helps maintain the efficacy of the medication and prevents deterioration.

Appearance

A hard capsule of dark green color containing yellow to pale yellow powder.

Package unit

30 capsules/bottle, 100 capsules/bottle