Viewing nowRoxocor (Roxoprofen Sodium Hydrate)
Loxoprofen Sodium Hydrate 68.1mg
Tablet · Prescription medication
Jungheon Pharmaceutical Co., Ltd.

MFDS item code 201902262 · Approved 2019.04.12 · Insurance code 053300610
Anti-inflammatory and analgesic effects for rheumatoid arthritis and osteoarthritis (degenerative arthritis), antipyretic and analgesic effects for acute upper respiratory tract infections.
This medication reduces inflammation and pain associated with various inflammatory conditions such as chronic rheumatoid arthritis, osteoarthritis, lower back pain, shoulder periarthritis, and cervical radiculopathy. It is also effective in alleviating inflammation and pain that occur after surgery, trauma, or tooth extraction. Furthermore, it reduces fever and pain that arise from acute infectious diseases such as acute upper respiratory tract infections. It is widely used to improve symptoms in conditions with various inflammation, pain, and fever symptoms.
1. In the case of efficacy/effect 1, 2 ○ Adults: Take 60 mg of Roxoprofen Sodium (anhydrous) orally three times a day. For one-time therapy, administer 60-120 mg orally at once. 2. In the case of efficacy/effect 3 ○ Adults: Take 60 mg of Roxoprofen Sodium (anhydrous) orally. In principle, it can be administered twice a day, with a maximum of 180 mg per day. It is advisable to avoid taking it on an empty stomach.
This medication may cause gastrointestinal bleeding in individuals who consume three or more alcoholic beverages daily, so it is essential to consult a physician or pharmacist. This medication may have cardiovascular effects and increase the risk of serious thrombotic responses such as myocardial infarction or stroke. Special caution is needed for patients with cardiovascular diseases or risk factors, and cardiovascular symptoms should be monitored closely during use. Additionally, this medication may increase the risk of serious gastrointestinal adverse reactions such as gastrointestinal bleeding, ulcers, and perforation. Elderly patients and those with a history of gastrointestinal diseases are at greater risk and should carefully monitor gastrointestinal symptoms during use. Patients with specific conditions such as peptic ulcers, severe heart failure, severe liver impairment, or severe kidney impairment should not take this medication, and those with hypersensitivity to aspirin or other non-steroidal anti-inflammatory drugs should also avoid administration. Patients with a history of peptic ulcers, blood diseases, liver and kidney diseases, elderly individuals, hypertensive patients, and women in early or mid-pregnancy should administer this medication with caution and consult a physician for appropriate measures if necessary. If allergic symptoms such as rash, itching, difficulty breathing, low blood pressure, gastrointestinal bleeding symptoms, severe abdominal pain, dizziness, or symptoms of liver dysfunction occur while taking this medication, you should immediately discontinue use and consult with medical personnel. This medication can cause adverse reactions such as liver dysfunction, renal impairment, blood disorders, and heart failure, thus regular testing may be necessary during use. Moreover, interactions can occur if taken together with other non-steroidal anti-inflammatory drugs, anticoagulants, diuretics, lithium, methotrexate, etc., so if you are taking other medications, you must inform your physician or pharmacist. This medication should not be taken during the late stages of pregnancy as it may pose risks to the fetus, and it is also safest for breastfeeding women to avoid using this medication. Safety has not been established for children, so it is advisable not to administer this medication to children. Elderly patients may experience adverse reactions more readily while taking this medication, so special caution is necessary. Lastly, this medication must be kept out of reach of children and transferring it to another container can negatively impact quality, so caution is advised.
Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, peptic ulcer, perforation, hematemesis, melena, bloody stools, shock, Stevens-Johnson syndrome, toxic epidermal necrolysis, erythema multiforme, acute generalized exanthematous pustulosis, aseptic meningitis (fever, headache, nausea, vomiting, neck stiffness, altered consciousness), severe allergic reactions, severe skin adverse reactions, respiratory problems.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly closed container to prevent exposure to air or moisture, and it is best kept at room temperature between 1 degree and 30 degrees Celsius. Proper storage will help maintain the efficacy of the medication for a longer period.
White round tablet
30 tablets/bottle, 300 tablets/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.