Viewing nowHyundai Loxoprofen Sodium Hydrate Tablet
Loxoprofen Sodium Hydrate 68.1mg
Tablet · Prescription medication
Hyundai Pharmaceutical Co., Ltd.

MFDS item code 201904648 · Approved 2019.07.10 · Insurance code 642004390
Anti-inflammatory and analgesic effects for chronic rheumatoid arthritis and osteoarthritis, and antipyretic and analgesic effects for acute upper respiratory infections.
This medication is used to relieve inflammation and pain associated with chronic rheumatoid arthritis, osteoarthritis, low back pain, shoulder periarthritis, and cervical radiculopathy. It is also effective in reducing inflammation and pain after surgery, trauma, or tooth extraction. Additionally, it alleviates fever and pain resulting from infectious diseases like acute upper respiratory infections. This medicine helps improve various kinds of pain and inflammation.
The recommended dose is 60 mg orally three times a day. For single-dose therapy, a dose of 60-120 mg may be administered orally. 60 mg should be taken orally. In principle, the maximum daily dose is 180 mg, administered two times a day. It is advisable to avoid taking this medication on an empty stomach. The dose may be adjusted according to symptoms.
This drug may cause gastrointestinal bleeding if taken by individuals who regularly consume more than three alcoholic beverages per day, so consultation with a doctor or pharmacist is essential. Patients with cardiovascular diseases or risk factors should be cautious as this medication may pose a risk of severe cardiovascular issues such as myocardial infarction or stroke. This drug can cause serious gastrointestinal adverse reactions, such as bleeding, ulcers, or perforations in the stomach or intestines, so especially elderly patients or those with a history of gastrointestinal diseases should use it with caution. Patients with a history of peptic ulcers, severe blood disorders, severe liver or kidney dysfunction, heart failure, or allergies to the ingredients of this drug should not take it. Individuals with a history of peptic ulcers, blood disorders, liver or kidney disease, heart failure, asthma, hypertension, elderly patients, etc., should be monitored more closely when using this drug. This drug may cause hypersensitivity reactions such as skin rashes, urticaria, shortness of breath, and low blood pressure; if these symptoms occur, discontinue use and seek medical attention immediately. If gastrointestinal symptoms such as abdominal pain, nausea, vomiting, diarrhea, or bloody stools occur, inform healthcare professionals immediately, and in severe cases, discontinue use. This drug may also cause neurological side effects such as drowsiness, dizziness, and headaches, so caution is advised when driving or operating machinery. Serious adverse reactions such as liver dysfunction, acute renal failure, hematuria, shortness of breath, and severe skin reactions have been rarely reported, so if there are any unusual symptoms during use, consult with a doctor immediately. This drug should be used at the lowest effective dose for the shortest duration; regular blood and liver/kidney function tests are recommended for long-term users. It is advisable not to take this medication concurrently with other non-steroidal anti-inflammatory drugs, and caution in use should be taken when combining it with specific blood pressure medications, diuretics, anticoagulants, etc.; inform your doctor before use. Pregnant women in the later stages should not use this drug, and during the early or middle stages of pregnancy, it should be used cautiously at the minimum dose under medical supervision. Lactating women should not take this medication, and safety for children has not been established, so it is preferable not to use it in pediatric patients. Elderly individuals are at higher risk of adverse reactions and should use this drug with greater caution, keeping it out of reach of children.
Urticaria, severe swelling (edema), tightness in the chest, difficulty breathing, shock, anaphylaxis-like symptoms, peptic ulcer, hematemesis, melena, bloody stools, intestinal perforation, jaundice, acute renal failure, hematuria, shortness of breath, asthma attacks, skin-mucous membrane syndrome (Stevens-Johnson syndrome), toxic epidermal necrolysis (Lyell syndrome), erythema multiforme, acute generalized exanthematous pustulosis, aseptic meningitis, angioedema, facial swelling, constriction of the small and large intestines, and lung issues.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a sealed container to protect it from air and moisture. Additionally, the drug should be kept away from excessively hot or cold places, ideally stored at room temperature between 1°C and 30°C.
Light pink round tablet
30 tablets/bottle, 500 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.