Medication info
Ryumael Capsule 7.5 mg (Meloxicam)

Ryumael Capsule 7.5 mg (Meloxicam)

Prescription medicationHard capsuleOral
Ingredient · strength
Meloxicam›7.5mg / 1 capsule
Manufacturer / importer
Hanlim Pharmaceutical Co., Ltd.
Appearance
Hard capsules with a greenish-brown color containing pale yellow powder
Packaging
30 capsules/bottle, 300 capsules/bottle
Approval status
Active

MFDS item code 200403532 · Notified 2004.09.14 · Insurance code 645300450

Summary

Main use
Relief of symptoms of rheumatoid arthritis, acute exacerbations of osteoarthritis, and ankylosing spondylitis
Who takes it
Adults
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 per day 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 per day depending on response to treatment. Do not administer more than 15 mg of this medicine per day, and take it with water or another beverage during a meal. In elderly patients or those at increased risk of adverse reactions, treatment is generally initiated at a dose of 7.5 mg per day. Patients with severe renal failure undergoing hemodialysis should not receive more than 7.5 mg per day.

Ingredients

Manufacturer
Hanlim Pharmaceutical Co., Ltd.

Efficacy & effects

Relief of symptoms of rheumatoid arthritis, acute exacerbations of osteoarthritis, and ankylosing spondylitis

  • Pain
  • motor impairment
  • osteoarthritis
  • rheumatoid arthritis
  • ankylosing spondylitis
View approved original text

This medication is used to treat symptoms related to various diseases of the joints, such as osteoarthritis, rheumatoid arthritis, and ankylosing spondylitis. In cases of osteoarthritis, it temporarily alleviates symptoms during acute exacerbations accompanied by pain and mobility dysfunction. Additionally, it helps relieve pain and inflammation in patients with rheumatoid arthritis and ankylosing spondylitis. Through these effects, it contributes to enhancing the patient's daily activity and reducing symptoms. Therefore, it is effectively used for the relief of arthritis symptoms.

How to take

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 per day 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 per day depending on response to treatment. Do not administer more than 15 mg of this medicine per day, and take it with water or another beverage during a meal. In elderly patients or those at increased risk of adverse reactions, treatment is generally initiated at a dose of 7.5 mg per day. Patients with severe renal failure undergoing hemodialysis should not receive more than 7.5 mg per day.

Precautions

This medication may cause gastrointestinal bleeding if taken by individuals who regularly consume more than three alcoholic drinks per day; therefore, it is essential to consult with a doctor or pharmacist. This drug can increase the risk of cardiovascular diseases, so patients with a history of heart disease or stroke, or those with risk factors, should exercise particular caution. If cardiovascular symptoms appear, the medication should be discontinued immediately, and a doctor should be consulted. It can cause serious gastrointestinal adverse reactions such as gastrointestinal bleeding, ulcers, and perforations, and particular caution should be exercised in elderly patients or those with a history of gastrointestinal diseases. If gastrointestinal symptoms or abnormalities occur, immediate evaluation and treatment by a doctor are necessary. This medication can cause severe skin reactions and life-threatening hypersensitivity reactions, so if symptoms such as skin rash or mucosal damage occur, it should be discontinued. It may affect kidney function; therefore, patients with kidney disease or impaired renal function should use it cautiously. Liver function abnormalities may occur, and those with liver disease or abnormal liver function test results should periodically check liver function. This medication may reduce reproductive capability, so women planning to become pregnant should avoid taking it. Patients with a history of hypersensitivity or allergy, particularly to aspirin or other non-steroidal anti-inflammatory drugs, should not take this medication. Patients with certain conditions such as gastrointestinal bleeding, active ulcers, severe liver dysfunction, renal impairment, heart failure, or severe hypertension should also avoid this drug. Elderly patients, those with skin adverse reactions, and patients with weakened kidney or liver function, or blood coagulation disorders, should take this medication carefully. This drug may interact with other medications, so it is essential to inform your doctor or pharmacist if you are taking other medications. Pregnant or breastfeeding women should not take this medication, and those who might become pregnant should also refrain from using it. In case of overdose, immediate medical attention is required, and since there is no specific antidote, emergency measures such as gastric lavage may be necessary. Keep this medication out of the reach of children and store it in its original container.

Side effects

Gastrointestinal hemorrhage, serious cardiovascular thrombotic reactions, myocardial infarction, stroke, bleeding from the stomach or intestine, ulcers, perforation, exfoliative dermatitis, mucocutaneous syndrome, toxic epidermal necrolysis, anaphylactic reaction, interstitial nephritis, glomerulonephritis, renal medullary necrosis, nephrotic syndrome, elevated serum transaminases, elevated 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, 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, cranial discomfort, fatigue, lethargy, taste dysfunction, mental clouding, seizures, sensory disturbances, tremor, blurred vision, visual impairment, conjunctivitis, foreign body sensation in the eye, subconjunctival hemorrhage, tinnitus, palpitations, elevated blood pressure, flush, facial flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina, heart failure, vasculitis, cough, upper respiratory tract infections, asthma, bronchial spasm, dyspnea, dyspepsia, nausea, vomiting, abdominal pain, constipation, bloating, diarrhea, loss of appetite, peptic ulcers, occult gastrointestinal bleeding, overt 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, itching, angioedema, vesicular dermatitis, erythema multiforme, photosensitive reactions, contact dermatitis, fixed drug eruption, urinary retention, elevated plasma creatinine levels, elevated urea levels, proteinuria, glucosuria, increased urinary sediment, hematuria, sodium and fluid retention, hyperkalemia, acute renal failure, decreased urine output, frequent urination, urinary tract infection, interstitial nephritis, edema, peripheral edema, lethargy, fever, facial edema, syncope, weight loss, weight gain, armpit and breast pain, arthralgia, low back pain, armpit and chest pain, rigidity, 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

Not everyone experiences these, and they can vary from person to person.

Storage

This medication is sensitive to light, so it should be stored in a container that does not allow light to enter. Additionally, it is best to store the medication at room temperature between 1 degree to 30 degrees Celsius. Proper storage will help maintain the efficacy of the medication.

Appearance and packaging

Appearance

Hard capsules with a greenish-brown color containing pale yellow powder

Package unit

30 capsules/bottle, 300 capsules/bottle

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.

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This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.