Viewing nowLorofen 60 mg (Loxoprofen Sodium Hydrate)
Loxoprofen Sodium Hydrate 68.1mg
Tablet · Prescription medication
Poonglim Pharm (Co., Ltd.)

MFDS item code 201804583 · Approved 2018.11.19 · Insurance code 649001840
Anti-inflammatory and analgesic effects for chronic rheumatic arthritis, osteoarthritis, and antipyretic and analgesic effects for acute upper respiratory tract infections
This medication exhibits anti-inflammatory and analgesic effects in conditions such as chronic rheumatic arthritis, osteoarthritis, low back pain, shoulder periarthritis, and cervical scapulohumeral syndrome. It is also used to reduce inflammation and alleviate pain following surgery, trauma, or tooth extraction. In cases of acute upper respiratory tract infections with accompanying fever, it demonstrates antipyretic and analgesic effects to improve patient symptoms. In summary, this drug is primarily used for the treatment of various types of arthritis and inflammatory diseases, pain after surgery or trauma, and relief of fever and pain in acute upper respiratory tract infections.
1. For indications 1 and 2: ○ Adults: Loxoprofen sodium (anhydrous) 60 mg orally three times daily. In single-dose therapy, 60-120 mg can be administered orally. 2. For indication 3: ○ Adults: Loxoprofen sodium (anhydrous) 60 mg is administered orally. Generally, it can be taken twice a day, with a maximum of 180 mg per day. It is preferred to avoid taking on an empty stomach.
This medication may pose a risk of gastric bleeding if taken by individuals who regularly consume alcohol in excess of three glasses a day, thus consultation with a doctor or pharmacist is necessary. This medication can affect the cardiovascular system, so individuals at risk of heart disease or stroke should be particularly cautious and report any cardiac symptoms to healthcare professionals immediately. Gastric bleeding or ulcers may occur, so senior patients or those with a history of gastrointestinal disorders should closely monitor their gastrointestinal status during treatment. Patients with peptic ulcers, severe blood disorders, serious liver or kidney disease, heart failure, allergies to aspirin or nonsteroidal anti-inflammatory drugs, pregnant women in the late stages of pregnancy, and breastfeeding mothers should not take this medication. Individuals with a history of peptic ulcers, blood disorders, or liver or kidney issues should follow healthcare professional guidance when taking this medication. This drug may cause hypersensitivity reactions such as skin rashes, itching, and urticaria, and such symptoms necessitate immediate cessation of the medication and consultation with a doctor. Gastrointestinal symptoms such as abdominal pain, vomiting, diarrhea, and dyspepsia may occur, and in severe cases, it may lead to bleeding or perforation, warranting immediate medical attention if symptoms are severe. Neurological symptoms such as dizziness, drowsiness, and headaches may also occur, necessitating caution while driving or operating machinery. Serious side effects such as abnormal liver function, decreased kidney function, and blood disorders may occur, thus regular blood tests and assessments of liver and kidney function are required. Taking this medication concurrently with other nonsteroidal anti-inflammatory drugs increases the risk of side effects, so co-administration should be avoided. Interactions may occur with certain blood pressure medications, anticoagulants, diuretics, and antidepressants, so any ongoing medications should be disclosed to healthcare professionals. Women in the early or middle stages of pregnancy must carefully consider the benefits and risks of this medication, and it should not be taken during the late stages of pregnancy. For breastfeeding mothers, it is safest not to take this medication as it may be transmitted through breast milk. Safety in pediatric patients has not been established, so its use in children is not recommended. Older adults have a higher likelihood of experiencing side effects, so extra caution is needed during administration, and their condition should be closely monitored after dosing. This medication should be kept out of reach of children, and transferring it to different containers is not advised as it may negatively affect the medication's quality.
Urticaria, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with fever, blisters, skin peeling, pain in oral/ocular mucosa, shortness of breath or difficulty breathing, asthma attacks, respiratory problems with cough and fever, jaundice (yellowing of skin or eyes), extreme lethargy, sudden and severe headache, thunderclap headache, seizures, confusion, visual disturbances, paralysis, urination issues
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly sealed container to prevent exposure to air or moisture. It is recommended to maintain a storage temperature between 1°C and 30°C to ensure the medication's effectiveness.
White round tablet
30 tablets/bottle, 600 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.