Viewing nowRoxonal Tablets (Sodium Loxoprofen Hydrate)
Loxoprofen Sodium Hydrate 68.1mg
Tablet · Prescription medication
Kyung Dong Pharmaceutical Co., Ltd.

MFDS item code 200301612 · Notified 2003.09.29 · Insurance code 648100560
Anti-inflammatory and analgesic effects for chronic rheumatoid arthritis and osteoarthritis, as well as antipyretic and analgesic effects for acute upper respiratory tract inflammation.
This medicine reduces inflammation and pain associated with chronic rheumatoid arthritis, osteoarthritis, low back pain, periarthritis of the shoulder, and cervical radiculopathy. It is also effective for alleviating inflammation and pain following surgery, trauma, or tooth extraction. It is used to reduce fever and pain resulting from infectious diseases such as acute upper respiratory infections. Thus, this drug helps improve various conditions related to inflammation, pain, and fever.
Administer 60 mg orally three times a day. For single-dose therapy, take 60-120 mg orally at one time. A maximum of 180 mg per day can be administered in two doses. It is preferable to avoid taking on an empty stomach. Adjust dosage according to symptoms.
Patients who regularly consume more than three alcoholic drinks per day should consult their doctor or pharmacist before taking this medication due to the risk of gastrointestinal bleeding. This drug may affect cardiovascular health, potentially increasing the risk of serious cardiovascular diseases such as myocardial infarction or stroke. Patients with a history of cardiovascular disease or risk factors should be particularly cautious, and if any cardiovascular symptoms occur, they should consult healthcare professionals immediately. This medication can cause serious gastrointestinal issues, so if gastrointestinal symptoms occur during treatment, immediate medical attention is necessary. Elderly patients or those with a history of gastrointestinal disease are at increased risk for gastrointestinal adverse effects and should be particularly cautious. Patients with peptic ulcers, severe blood disorders, liver dysfunction, kidney dysfunction, heart failure, individuals with hypersensitivity to this drug, and those allergic to aspirin or other non-steroidal anti-inflammatory drugs should not use this medication. Pregnant women in the late stages of pregnancy, nursing mothers, patients with inflammatory bowel disease, and those with lactose intolerance should also refrain from using this drug. Individuals with a history of peptic ulcers, blood disorders, liver dysfunction, kidney dysfunction, hypertension, and elderly patients should take precautions when using this drug, and should follow their doctor's instructions for continued treatment if necessary. If any allergic symptoms such as rash, itching, difficulty breathing, or low blood pressure occur during use, discontinue use immediately and notify medical personnel. Gastrointestinal symptoms such as abdominal pain, nausea, vomiting, or diarrhea may arise, so prompt medical care is warranted for any unusual symptoms. This drug may cause central nervous system symptoms such as drowsiness, dizziness, or headache, so caution is advised when driving or operating machinery. Long-term use may impact liver or kidney function, necessitating regular blood tests and liver and kidney function assessments. There may be interactions with other drugs, so inform your doctor or pharmacist if you are taking any other medications. Particular caution is needed when taken with blood pressure medications, diuretics, anticoagulants, lithium, methotrexate, etc. Usage during early and mid-pregnancy should be cautious, and it should not be used in the late stages of pregnancy due to potential fetal risks. It is advisable not to take this medication while breastfeeding. Safety in children has not been established, so its use in children is generally not recommended. Elderly individuals are at higher risk of adverse reactions and should exercise additional caution when using this drug. This drug should be kept out of reach of children and should not be transferred to other containers.
Hives, severe swelling (edema), chest tightness, difficulty breathing, shock, anaphylactic-like symptoms, peptic ulcer, perforation, hematemesis, melena, gastrointestinal bleeding accompanied by shock, intestinal perforation, liver dysfunction (including jaundice), fulminant hepatitis, acute renal failure, nephrotic syndrome, interstitial nephritis, hematuria, proteinuria, interstitial pneumonia, asthma attacks, skin and mucous membrane syndrome (Stevens-Johnson syndrome), toxic epidermal necrolysis (Lyell syndrome), and others.
Not everyone experiences these, and they can vary from person to person.
This medication must be stored in a tightly sealed container to avoid exposure to air and moisture. It is important to maintain a storage temperature between 1 and 30 degrees Celsius. Proper storage will help ensure the safety and effectiveness of the drug.
White to pale yellow round tablets
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.