Meloxikam Capsule 15 Milligrams (Meloxicam)

Adult dosage

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 up to 15 mg daily as needed. 2. Rheumatoid arthritis, ankylosing spondylitis: ○ Adults: Administer 15 mg of this drug orally once daily. The dose may be reduced to 7.5 mg daily depending on the response to treatment. This drug should not be administered at doses exceeding 15 mg daily, and should be taken with water or another beverage during a meal. ○ In elderly patients 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.

This drug can cause gastrointestinal bleeding if taken by individuals who regularly consume more than three glasses of alcohol daily, so consultation with a doctor or pharmacist is essential. This drug may increase the risk of cardiovascular diseases, so individuals with a history of heart disease or stroke, or those with risk factors, should use it with caution. If symptoms such as chest pain, shortness of breath, weakness, or slurred speech occur, the medication should be immediately discontinued and a physician consulted. This drug can lead to serious conditions such as gastrointestinal bleeding, ulcers, or perforations, so individuals with a history of gastrointestinal diseases or the elderly should be particularly careful. If gastrointestinal pain, black stools, or blood in vomit occurs during use, immediate medical attention is required. Severe skin reactions such as rash, blisters, or mucosal damage can occur, so if any skin abnormalities occur, the medication should be promptly discontinued. Individuals with kidney or liver function issues should regularly monitor their kidney and liver function while using this medication, and consult a physician if any abnormal symptoms arise. This drug may impair reproductive ability, so women planning on becoming pregnant should avoid using it. Individuals allergic to this drug or with hypersensitivity to aspirin or other nonsteroidal anti-inflammatory drugs should not use it. Pregnant women or women who may become pregnant, as well as breastfeeding women, should not take this medication. This drug may affect blood coagulation, so individuals taking anticoagulants or blood-related medications should exercise caution. Drug interactions may occur, so inform the physician or pharmacist of any medications being used. The elderly may have reduced kidney, liver, and heart function, so they should use the minimal effective dose and be vigilant for abnormal symptoms. In cases of overdose, symptoms such as nausea, vomiting, drowsiness, and gastrointestinal bleeding may occur; therefore, dosing should be strictly adhered to, and immediate medical assistance should be sought in the case of overdose. Keep out of reach of children and store in the original container sealed properly.

Gastrointestinal bleeding, serious cardiovascular thrombotic reactions, myocardial infarction, stroke, bleeding of the stomach or intestines, ulcers, perforation, exfoliative dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis, anaphylactic reactions, interstitial nephritis, glomerulonephritis, renal medullary necrosis, nephrotic syndrome, elevation of 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, lowered hematocrit, increased neutrophils, increased eosinophils, increased basophils, increased monocytes, agranulocytosis, anaphylaxis, malaise, confusion, disorientation, mood changes, mood disorders, insomnia, nightmares, anxiety, increased appetite, depression, irritability, dizziness, drowsiness, headache, pressure in the head, fatigue, lethargy, taste dysfunction, mental confusion, convulsions, sensory disturbances, tremors, blurred vision, conjunctivitis, sensation of foreign body in the eye, scleral hemorrhage, tinnitus, palpitations, elevated blood pressure, flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina, heart failure, vasculitis, cough, upper respiratory tract infection, asthma, bronchospasm, dyspnea, dyspepsia, nausea, vomiting, abdominal pain, constipation, bloating, diarrhea, loss of appetite, peptic ulcer, occult gastrointestinal bleeding, gross gastrointestinal bleeding, stomatitis, gastritis, esophagitis, belching, dry mouth, thirst, angular cheilitis, occult blood in urine, gastrointestinal perforation, colitis, pancreatitis, black stools, perforated peptic ulcer, hepatitis, jaundice, liver failure, alopecia, increased sweating, skin rash, urticaria, itching, angioedema, bullous dermatitis, erythema multiforme, photosensitivity reactions, contact dermatitis, dysuria, elevated plasma creatinine, increased urea levels, changes in renal function tests, total protein decrease, decreased albumin, proteinuria, glycosuria, increased urinary sediment, hematuria, sodium and fluid retention, hyperkalemia, acute renal failure, decreased urine output, frequent urination, urinary tract infections, interstitial nephritis, edema, edema of lower limbs, fatigue, fever, facial swelling, syncope, weight loss, weight gain, axillary breast pain, arthralgia, low back pain, axillary chest pain, rigidity, lower limb weakness, decreased female reproductive ability, dehydration

This medication is sensitive to light and should be stored in a special container that does not allow light in. Additionally, it's important to maintain a storage temperature between 1 degree and 30 degrees Celsius to preserve the medication's efficacy.

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, 300 capsules/bottle