Melvicam Capsule 7.5 mg (Meloxicam)

Adult dose

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. 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 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 generally started at a dose of 7.5 mg daily. ○ Patients with severe renal impairment receiving hemodialysis must not receive more than 7.5 mg daily.

This medication can cause gastrointestinal bleeding in individuals who regularly consume more than three alcoholic beverages daily, so it is essential to consult a physician or pharmacist. This drug may affect the cardiovascular system and increase the risk of serious cardiovascular events such as myocardial infarction or stroke; therefore, individuals with a history of cardiovascular disease or risk factors should be monitored closely. Caution is particularly necessary for individuals with a history of gastrointestinal disease or the elderly, as serious problems such as bleeding, ulcers, or perforations in the stomach or intestines may occur. This medication can cause severe allergic reactions or dermatitis; if any abnormal skin symptoms arise, discontinue use immediately and consult a physician. Since it can affect kidney and liver function, individuals with kidney or liver disease should consult their healthcare provider before taking this medication, and regular check-ups are necessary during usage. Women planning to become pregnant or who may be pregnant should avoid using this drug as it may impair fertility, and it should not be taken during pregnancy. Individuals with known allergies or hypersensitivity to aspirin and other non-steroidal anti-inflammatory drugs should not take this medication. If symptoms such as gastrointestinal bleeding, cardiovascular symptoms, skin rashes, or respiratory distress occur during treatment, seek medical attention immediately. Use the minimal effective dose for the shortest duration to reduce the risk of side effects, and patients on long-term treatment should undergo regular blood tests and kidney and liver function evaluations. There may be interactions with other medications, so inform your healthcare provider of any current medications being taken, particularly if using anticoagulants, diuretics, lithium, or methotrexate. This drug can cause drowsiness or dizziness, so caution is advised when driving or operating machinery. Serious side effects may occur in the event of overdose, so follow the prescribed dosage exactly, and if overdose is suspected, seek medical attention immediately. Keep this medication out of reach of children and store it in its original container to prevent quality deterioration or misuse.

Gastrointestinal bleeding, serious cardiovascular thrombotic reactions, myocardial infarction, stroke, bleeding from the stomach or intestines, ulcers, perforation, exfoliative dermatitis, mucocutaneous syndrome, toxic epidermal necrolysis, anaphylactic reactions, interstitial nephritis, glomerulonephritis, medullary kidney 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, reduced hemoglobin, reduced hematocrit, increased neutrophils, increased eosinophils, increased basophils, increased monocytes, agranulocytosis, anaphylaxis, anaphylactoid reactions, malaise, confusion, loss of orientation, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, irritability, dizziness, drowsiness, headache, cephalgia, fatigue, lethargy, taste dysfunction, mental fog, seizures, sensory disturbances, tremors, blurred vision, visual impairment, conjunctivitis, foreign body sensation in the eye, scleral hemorrhage, tinnitus, palpitations, elevated blood pressure, flushing, facial flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina pectoris, heart failure, vasculitis, cough, upper respiratory tract infection, asthma, bronchial spasm, dyspnea, dyspepsia, nausea, vomiting, abdominal pain, constipation, abdominal 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 stool, gastrointestinal perforation, colitis, pancreatitis, melena, perforated peptic ulcer, hepatitis, vascular edema, vesicular dermatitis, erythema multiforme, photosensitivity reactions, contact dermatitis, fixed drug eruption, urinary disturbances, 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 axilla/breasts, arthralgia, low back pain, pain in axilla/chest, rigidity, lower limb weakness, decreased female reproductive ability, dehydration

This medication is sensitive to light, so it should be stored in a container that does not allow light to enter. Additionally, it is important to maintain a temperature between 1 and 30 degrees Celsius when storing the medication. This helps preserve its effectiveness and ensures safe usage.

Appearance

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

Package unit

30 capsules/bottle, 300 capsules/bottle