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

MFDS item code 201802417 · Approved 2018.06.11 · Insurance code 057000120
Anti-inflammatory and analgesic effects for chronic rheumatoid arthritis and osteoarthritis, as well as antipyretic and analgesic effects for acute upper respiratory inflammation.
This medication helps reduce inflammation and alleviate pain in conditions such as chronic rheumatoid arthritis, osteoarthritis, low back pain, shoulder periarthritis, and cervical radiculopathy. It also effectively reduces inflammation and pain following surgery, trauma, and tooth extraction. It improves symptoms of infections such as acute upper respiratory inflammation through its antipyretic and analgesic effects. This drug is used for a variety of inflammatory and pain-related conditions and symptoms.
1. For efficacy 1 and 2: ○ Adults: Loxoprofen Sodium (anhydrous) 60 mg is taken orally three times daily. For a single dose, 60-120 mg may be taken orally. 2. For efficacy 3: ○ Adults: Loxoprofen Sodium (anhydrous) 60 mg is taken orally. As a rule, it can be given twice a day, with a maximum daily dose of 180 mg. Avoid taking on an empty stomach.
This medication may cause gastrointestinal bleeding in individuals who regularly consume more than three alcoholic drinks daily, so it is essential to consult a doctor or pharmacist. This medication may increase the risk of cardiovascular diseases, so patients with a risk of heart disease or stroke should be particularly cautious, and if cardiovascular symptoms appear, they should immediately consult medical personnel. It may cause serious gastrointestinal issues such as gastrointestinal bleeding, ulceration, or perforation, hence elderly patients or those with a history of gastrointestinal disease should be especially careful. Patients with peptic ulcers, severe liver or kidney impairments, severe blood disorders, or heart failure should not take this medication. Patients with asthma or allergies to aspirin, pregnant women in late pregnancy, and nursing mothers should also avoid using this drug. If hypersensitivity reactions such as rash, itching, or urticaria occur, discontinue use immediately and inform medical personnel. If gastrointestinal symptoms such as abdominal pain, vomiting, or blood in stools occur, stop taking the medication and seek treatment. Caution is needed when driving or operating machinery as neurological symptoms such as drowsiness, dizziness, and headaches may occur. Patients with impaired liver or kidney function should undergo regular examinations and discontinue use if any abnormal signs appear. This medication should not be taken together with other NSAIDs as it increases the risk of side effects. It may interact with specific antihypertensive drugs, diuretics, anticoagulants, and antibiotics, so inform your doctor if you are taking such medications. Women in early and mid-pregnancy should carefully decide on the necessity of this medication, and it should never be used in late pregnancy. Safety in pediatric patients has not been established, so use in children is not recommended. Elderly individuals are at a higher risk of side effects, so extra caution is necessary when administering. This medication should be used at the minimum effective dose and for the shortest duration necessary, and any unusual symptoms during treatment should be immediately consulted with medical personnel. Store out of reach of children and do not transfer to other containers for safety.
Urticaria, severe swelling (angioedema, facial swelling, periocular edema, oral swelling), chest tightness, difficulty breathing, asthma attacks, shock, anaphylaxis-like symptoms, gastrointestinal bleeding (vomiting blood, bleeding stools, blood in stools), severe gastrointestinal adverse reactions (peptic ulcers, perforation, bowel perforation), skin and mucous membrane syndrome (Stevens-Johnson syndrome), toxic epidermal necrolysis (Lyell syndrome), lupus erythematosus, and aseptic meningitis due to mixed connective tissue disease.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly sealed container to protect it from air and moisture. It is also important to store it at room temperature between 1°C and 30°C to maintain its effectiveness.
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.