Dextaron Tablets 400 mg (Dexibuprofen D.C.)

Adult dose

Adults: Administer dexibuprofen 400 mg orally 2～3 times daily. Do not exceed 1,200 mg of dexibuprofen per day.

Caution should be exercised when this medication is taken by individuals who regularly consume more than 3 alcoholic drinks a day, as it may increase the risk of gastrointestinal bleeding, and consultation with a doctor or pharmacist is essential. This drug may affect the cardiovascular system and can increase the risk of myocardial infarction and stroke, so it should be used cautiously in those with cardiovascular diseases or risk factors. This medication can cause serious adverse reactions, including gastrointestinal bleeding, ulcers, and perforations, particularly in the elderly or those taking it for prolonged periods, therefore caution is needed. Individuals with a history of gastrointestinal ulcers or bleeding or severe liver, kidney, or heart diseases should avoid taking this drug. Taking it with aspirin or other non-steroidal anti-inflammatory drugs (NSAIDs) can increase the risk of gastrointestinal bleeding and reduce the drug's effectiveness, so co-administration should be avoided. During treatment, it is recommended to stop breastfeeding or discontinue the medication, as dizziness or fatigue may occur, necessitating caution when driving or operating machinery. People with blood disorders, liver problems, kidney issues, high blood pressure, heart failure, or those who are elderly or pregnant should consult a professional before taking this medication. This drug can interact with several other medications, so consultation with a professional is advised if other drugs are being taken. If severe allergic reactions, skin rashes, shortness of breath, gastrointestinal symptoms, or blood disorders occur during treatment, the medication should be stopped immediately, and medical consultation should be sought. During pregnancy, especially after the 6th month, it may be harmful to the fetus, so use should be avoided; women in early pregnancy or planning pregnancy should also consult a professional. When taking, the lowest effective dose and shortest duration should be used, and regular checks on liver and kidney function as well as blood status should be conducted for long-term users. In the case of overdose, immediate medical attention should be sought for appropriate treatment. This drug should be kept out of reach of children, protected from direct sunlight, and stored in a cool, dry place.

Gastrointestinal bleeding, serious cardiovascular thrombotic reactions, myocardial infarction, stroke, gastrointestinal or intestinal bleeding, ulcers, perforations, dizziness, fatigue, headache, shock, chest discomfort, chills, dyspnea, hypotension, aplastic anemia, hemolytic anemia, granulocytopenia, leukopenia, agranulocytosis, pancytopenia, thrombocytopenia, impaired platelet function, eosinophilia, dyspepsia, abdominal distension, heartburn, pain in the upper abdomen, diarrhea, constipation, loss of appetite, nausea, vomiting, abdominal pain, discomfort in the stomach, esophagitis, esophageal stricture, diverticulitis exacerbation, nonspecific hemorrhagic colitis, ulcerative colitis, Crohn's disease, peptic ulcer, gastrointestinal bleeding, perforation, blood in stools, gastritis, pancreatitis, thirst, stomatitis, erythema multiforme, systemic lupus erythematosus, alopecia, angioedema, mucocutaneous syndrome, Stevens-Johnson syndrome, toxic epidermal necrolysis, eosinophilia, systemic syndromes, drug rash, acute generalized pustular psoriasis, rash, urticaria, itching, purpura, asthma attacks, eczema, anaphylaxis reaction, photosensitivity reactions, jaundice, elevated ALT, elevated AST, elevated ALP, liver dysfunction, hepatitis, rhinitis, bronchospasm, acute pneumonia, disregard, cancer infiltration, visual impairment, hearing loss, tinnitus, taste disturbances, fatigue, drowsiness, headache, dizziness, anxiety, restlessness, confusion, depression, aseptic meningitis, mental disturbances, nervousness, excitability, disorientation, reversible toxic amblyopia, hypotension, hypertension, palpitations, acute renal failure, oliguria, hematuria, proteinuria, elevated BUN, elevated serum creatinine, hyperkalemia, decreased urine output, generalized edema, shortness of breath, lethargy, renal papillary necrosis, nephrotic syndrome, interstitial nephritis, peripheral edema, acute pulmonary edema, fluid retention, edema, hypertension, heart failure, Cournand's syndrome, reduced reproductive capacity in women, periorbital edema, lethargy, fever, nosebleeds, exacerbation of inflammation, increased urea nitrogen, increased transaminases, increased alkaline phosphatase, decreased hemoglobin, decreased hematocrit, reduced platelet aggregation, prolonged bleeding time, anaphylaxis-like reaction, exfoliative dermatitis, mucocutaneous syndrome, toxic epidermal necrolysis, asthma, aspirin-sensitive asthma, temporary infertility, oligohydramnios, neonatal renal impairment

This medication may be sensitive to air or moisture, so it should be stored in a sealed container. Additionally, it is best kept at room temperature between 1°C and 30°C.

Appearance

White rectangular film-coated tablets

Package unit

30 tablets/bottle, 300 tablets/bottle