Viewing nowLoxofil Tablet (Sodium Loxoprofen Hydrate)
Loxoprofen Sodium Hydrate 68.1mg
Tablet · Prescription medication
iWorld Pharmaceutical Co., Ltd.

MFDS item code 201603025 · Approved 2016.05.30 · Insurance code 669604560
Anti-inflammatory and analgesic effects for chronic rheumatoid arthritis and osteoarthritis
This medication helps relieve inflammation and pain associated with chronic rheumatoid arthritis, osteoarthritis, lower back pain, adhesive capsulitis, and shoulder periarthritis. It also reduces inflammation and pain after surgery, trauma, and tooth extraction. It is effective in treating acute upper respiratory inflammation and the associated fever and pain. By exerting anti-inflammatory, analgesic, and antipyretic effects in these various conditions and situations, it alleviates the discomfort of patients and improves symptoms.
1. For indications 1 and 2 ○ Adults: Administer Sodium Loxoprofen (anhydrous) 60 mg orally three times a day. For single therapy, take 60–120 mg orally. 2. For indication 3 ○ Adults: Administer Sodium Loxoprofen (anhydrous) 60 mg orally. In principle, it can be taken twice a day, with a maximum daily dose of 180 mg.
Individuals who regularly consume more than three alcoholic beverages a day should consult a doctor or pharmacist before taking this medication. Drinking alcohol while on this medication may increase the risk of gastrointestinal bleeding. This medication, along with other non-steroidal anti-inflammatory drugs, may increase the risk of cardiovascular diseases, so caution is needed for individuals with heart disease or risk factors. If cardiovascular symptoms occur, immediate medical attention is necessary, and patients should be informed about these symptoms and how to respond to them in advance. Additionally, this medication can lead to severe gastrointestinal adverse reactions such as gastrointestinal bleeding, ulcers, and perforation, hence those with a history of gastrointestinal disease and the elderly should be particularly cautious. If gastrointestinal bleeding symptoms or severe abdominal pain occur while taking this medication, cease use immediately and consult a physician. Those with certain conditions such as peptic ulcers, severe blood disorders, liver dysfunction, kidney dysfunction, or heart failure should not take this medication. Individuals with allergic reactions to aspirin or other non-steroidal anti-inflammatory drugs, or those with a history of asthma should also refrain from using this medication. 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 or diseases such as hypertension, kidney disease, liver disease, or asthma should use this medication cautiously under the guidance of a physician. This medication may cause various side effects including allergic reactions, skin rashes, gastrointestinal symptoms, liver dysfunction, and kidney impairment; if any unusual symptoms occur, discontinue use immediately and consult a doctor. Immediate emergency measures are required if severe skin rashes or allergic symptoms such as difficulty breathing or hives occur. This medication should be taken at the minimum effective dose for the shortest duration, and if used long-term, regular blood tests and liver and kidney function tests are necessary. Elderly patients or those with chronic conditions require more careful monitoring. It is advisable not to take this medication alongside other non-steroidal anti-inflammatory drugs, as it may interact with specific medications; hence it is crucial to inform the physician of any other medications being taken. Women who are pregnant or may become pregnant should consult a physician before use, and should strictly avoid it during late pregnancy. Nursing mothers should also refrain from taking this medication. Safety in children has not been established, so it is recommended not to use it in pediatric patients. This medication should be kept out of reach of children and should not be transferred to other containers.
Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, peptic ulcer, perforation, hematemesis, melena, shock, Stevens-Johnson syndrome, toxic epidermal necrolysis (Lyell syndrome), erythema multiforme, acute generalized exanthematous pustulosis, jaundice, acute kidney failure, interstitial nephritis, difficulty breathing, asthma attacks, aseptic meningitis, severe allergic reactions, cardiovascular thrombotic reactions, myocardial infarction
Not everyone experiences these, and they can vary from person to person.
This medication may be sensitive to air and moisture, so it should be stored in a sealed container. It is recommended to maintain a storage temperature between 1 degree and 30 degrees Celsius.
White circular tablet
30 tablets/bottle, 100 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.