Medication info

Samsung Meloxicam Capsule 7.5 mg

Prescription medicationHard capsuleOralExpired
Ingredient · strength
Meloxicam›7.5mg / 1 capsule
Manufacturer / importer
Samsung Pharm Co., Ltd.
Appearance
A hard capsule with upper and lower green parts filled with a pale yellow contents.
Packaging
30 capsules/bottle, 300 capsules/bottle
Approval status
Expired

MFDS item code 201901931 · Approved 2019.03.29

This product's status changed to Expired on 2024.03.29. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Relief of symptoms of rheumatoid arthritis, acute exacerbations of osteoarthritis (short-term), and ankylosing spondylitis
Who takes it
Adults
Adult dose
1. Acute exacerbation of osteoarthritis (degenerative joint disease): ○ 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 medication orally once daily. The dose may be reduced to 7.5 mg per day depending on the response to treatment. This medication must not be administered at doses exceeding 15 mg per day, and should be taken with water or another beverage during a meal. ○ In older adults or individuals at increased risk of adverse reactions, treatment is usually initiated at a dose of 7.5 mg per day. ○ Patients with severe renal failure who are receiving hemodialysis must not receive more than 7.5 mg per day.

Ingredients

Manufacturer
Samsung Pharm Co., Ltd.

Efficacy & effects

Relief of symptoms of rheumatoid arthritis, acute exacerbations of osteoarthritis (short-term), and ankylosing spondylitis

  • Pain
  • motor coordination disorder
  • osteoarthritis
  • acute exacerbation
  • rheumatoid arthritis
  • ankylosing spondylitis
View approved original text

This medication is used to relieve pain and motor dysfunction in short term during acute exacerbation of osteoarthritis, as well as to treat symptoms caused by rheumatoid arthritis and ankylosing spondylitis.

How to take

Adult dose

1. Acute exacerbation of osteoarthritis (degenerative joint disease): ○ 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 medication orally once daily. The dose may be reduced to 7.5 mg per day depending on the response to treatment. This medication must not be administered at doses exceeding 15 mg per day, and should be taken with water or another beverage during a meal. ○ In older adults or individuals at increased risk of adverse reactions, treatment is usually initiated at a dose of 7.5 mg per day. ○ Patients with severe renal failure who are receiving hemodialysis must not receive more than 7.5 mg per day.

Precautions

This medication may pose a risk of gastrointestinal bleeding in individuals who regularly consume more than three drinks a day; therefore, consultation with a physician or pharmacist is essential. This medication can affect the cardiovascular system and may increase the risk of serious cardiovascular diseases such as myocardial infarction or stroke. Caution is necessary for those with a history of cardiovascular disease or risk factors, and if symptoms such as chest pain or shortness of breath occur, discontinue use immediately. This medication can also cause serious gastrointestinal side effects such as gastrointestinal bleeding, ulcers, and perforation, particularly in elderly patients or individuals with a history of gastrointestinal disease, who should use it cautiously. Severe skin reactions may occur, so if symptoms such as rash or mucosal damage appear, discontinue use immediately and seek medical attention. There may occasionally be abnormal liver or kidney function; consult a doctor immediately if there are any symptoms or if there is a history of liver or kidney disease. Women planning to become pregnant or those who may be pregnant should avoid this medication as it may impair fertility, and it should also not be used during pregnancy or breastfeeding. This medication should not be administered to individuals with specific allergies or a history of asthma, and it is contraindicated in cases of gastrointestinal bleeding or serious liver/kidney impairment. Regular monitoring of blood pressure, kidney function, and liver function is advisable during treatment, and any unusual symptoms should be reported to medical professionals immediately. It is recommended not to use this medication with other non-steroidal anti-inflammatory drugs, and caution is warranted when taken with aspirin, anticoagulants, or diuretics due to increased risks of bleeding or worsening kidney function. In cases of overdose, drowsiness, nausea, vomiting, gastrointestinal bleeding may occur, and in severe cases, renal failure, liver failure, or respiratory depression can happen, necessitating immediate emergency care. Store out of reach of children and keep sealed in the original container. When taking this medication, use the minimum effective dose for the shortest duration required and consult a physician or pharmacist immediately if any adverse reactions occur.

Side effects

Gastrointestinal hemorrhage, serious cardiovascular thrombotic reactions, myocardial infarction, stroke, bleeding from the stomach or intestines, ulcers, perforation, exfoliative dermatitis, mucous membrane syndrome, toxic epidermal necrolysis, anaphylactic reactions, interstitial nephritis, glomerulonephritis, renal 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 counts, leukopenia, thrombocytopenia, anemia, decreased plasma iron, reduced hemoglobin, decreased 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, scalp sensation, fatigue, lethargy, taste dysfunction, mental confusion, seizures, sensory abnormalities, tremors, visual disturbances, conjunctivitis, foreign body sensation in the eye, subconjunctival hemorrhage, tinnitus, palpitations, hypertension, flushing, facial flushing, arrhythmia, tachycardia, hypotension, hypertension, myocardial infarction, angina pectoris, heart failure, vasculitis, cough, upper respiratory tract infections, asthma, bronchospasm, dyspnea, dyspepsia, nausea, vomiting, abdominal pain, constipation, bloating, diarrhea, loss of appetite, peptic ulcer, occult gastrointestinal bleeding, 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, elevated plasma transaminase concentrations, increased bilirubin, jaundice, liver failure, alopecia, increased sweating, skin rash, urticaria, itching, angioedema, vesicular dermatitis, erythema multiforme, photosensitive reactions, contact dermatitis, urinary disturbances, elevated plasma creatinine levels, increased urea levels, decreased total protein, reduced albumin, proteinuria, glycosuria, increased urinary sediment, hematuria, sodium and fluid retention, hyperkalemia, acute renal failure, decreased urine output, frequency of urination, urinary tract infections, interstitial nephritis, edema, peripheral edema, malaise, fever, facial edema, syncope, weight loss, weight gain, pain in the axilla and breast, arthralgia, low back pain, pain in the axilla and chest, stiffness, lower limb weakness, decreased female fertility, dehydration

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

Storage

This medication is sensitive to light and should be stored in a container that prevents light exposure. It should be stored at room temperature between 1 to 30 degrees Celsius to maintain efficacy.

Appearance and packaging

Appearance

A hard capsule with upper and lower green parts filled with a pale yellow contents.

Package unit

30 capsules/bottle, 300 capsules/bottle

Same-ingredient medicines

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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.