Viewing nowRoxofen Tablets (Sodium Loxoprofen Hydrate)
Loxoprofen Sodium Hydrate 68.1mg
Tablet · Prescription medication
Joah Pharmaceutical Co., Ltd.

MFDS item code 201405365 · Approved 2014.11.18 · Insurance code 644602990
Anti-inflammatory and analgesic effects for chronic rheumatoid arthritis, osteoarthritis, and fever and pain relief for acute upper respiratory infections.
This medication is used to relieve inflammation and pain caused by various inflammatory and degenerative joint diseases such as chronic rheumatoid arthritis, osteoarthritis, lower back pain, shoulder periarthritis, and cervical syndrome. It also helps reduce inflammation and pain arising from conditions such as postoperative, post-traumatic, and post-extraction states. It improves symptoms through antipyretic and analgesic actions, especially in cases of acute upper respiratory infections, particularly when complicated by bronchitis. Overall, this medicine is effectively used for various inflammatory diseases, as well as pain and fever symptoms.
1. For indications 1 and 2 ○ Adults: Administer 60 mg of sodium loxoprofen (anhydrous) orally three times a day. In a single-dose regimen, take 60-120 mg orally. 2. For indications 3 ○ Adults: Administer 60 mg of sodium loxoprofen (anhydrous) orally. In principle, it can be taken twice a day, with a maximum daily dose of 180 mg. It is advisable to take it on an empty stomach.
Individuals who regularly consume three or more drinks a day should consult with a doctor or pharmacist before taking this medication because it can cause gastrointestinal bleeding. This medication can increase the risk of cardiovascular diseases, thus those with a history of heart disease or stroke, or risk factors related to them should exercise particular caution. Immediate medical attention should be sought if cardiovascular symptoms arise during use. There is a risk of serious gastrointestinal problems such as gastrointestinal bleeding, ulcers, and perforation. Elderly patients or those with a history of gastrointestinal diseases should take this medication more cautiously, and should discontinue use and consult with medical personnel if symptoms of gastrointestinal bleeding occur. Individuals with a history of peptic ulcers, severe blood abnormalities, severe liver or kidney dysfunction, congestive heart failure, allergies to this medication or its ingredients, a history of allergic reactions to aspirin or other non-steroidal anti-inflammatory drugs, pregnant women in late pregnancy, nursing mothers, and patients with inflammatory bowel disease should not take this medication. Patients with a history of peptic ulcers, blood abnormalities, liver or kidney diseases, heart failure, asthma, hypertension, the elderly, or those on anticoagulants should take this medication with caution and closely monitor their conditions during use. If allergic symptoms such as rash, itching, difficulty breathing, or hives occur while taking this medication, it should be discontinued immediately and medical personnel notified. If gastrointestinal symptoms such as abdominal pain, hematemesis, bloody stools, nausea, or vomiting occur, the medication should be discontinued immediately, and treatment should be sought. This medication may cause neurological symptoms such as drowsiness, dizziness, and headache, so caution should be exercised when driving or operating machinery. There may be occurrences of liver or kidney dysfunction, symptoms of heart failure, blood abnormalities, etc., hence regular monitoring is necessary, and the medication should be discontinued if any abnormal symptoms are observed. This medication should not be taken with other non-steroidal anti-inflammatory drugs and may interact with certain blood pressure medications, anticoagulants, antibiotics, etc., so be sure to inform about any other medications being taken. During pregnancy, especially in the late stage, it may be harmful to the fetus, thus should not be taken, and it is advisable to also avoid using during breastfeeding. Safety for children has not been established, hence use is not recommended. Elderly individuals are at a higher risk for adverse reactions; therefore, special care should be taken when using this medication. This medication should be kept out of reach of children and should not be transferred to another container.
Hives, severe swelling (edema), chest tightness, difficulty breathing, shock, anaphylaxis-like symptoms, digestive tract bleeding, perforation, dyspnea, skin and mucous membrane syndrome (Stevens-Johnson syndrome), toxic epidermal necrolysis (Lyell syndrome), erythema multiforme, acute generalized exanthematous pustulosis, liver dysfunction (including jaundice), fulminant hepatitis, acute renal failure, dyspnea, asthma attacks, severe edema, increased blood pressure, aseptic meningitis, severe.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly sealed container to prevent air or moisture from entering. It is recommended to store at room temperature between 1 and 30 degrees Celsius.
Pink round tablets
30 T/bottle, 500 T/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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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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For anything that needs medical judgment, consult a doctor or pharmacist.
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.