Dibuprofen 400 mg (Dexibuprofen D.C.)

Adult dose

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

This drug may pose a risk of gastrointestinal bleeding if taken by individuals who regularly consume more than 3 alcoholic beverages a day; consultation with a doctor or pharmacist is essential. This drug can impact the cardiovascular system, potentially increasing the risk of serious thrombotic events such as myocardial infarction or stroke. Patients with a history of cardiovascular disease or risk factors should exercise heightened caution. Elderly patients or those with a history of gastrointestinal diseases should take special care, as this medication may lead to serious gastrointestinal issues such as ulcers, bleeding, or perforation. Patients with gastrointestinal ulcers or bleeding, blood disorders, severe impairment of liver or kidney function, severe heart failure, hypertension, or those allergic to this medication should not take it. Co-administration with aspirin or other non-steroidal anti-inflammatory drugs (NSAIDs) may increase the risk of gastrointestinal bleeding, so it is advisable not to combine them. Pregnant women after six months of pregnancy should avoid taking this medication as it may harm the fetus. During treatment, caution is advised while driving or operating machinery due to the risk of dizziness or fatigue causing accidents. This medication can also be transferred through breast milk, potentially causing serious adverse reactions in infants, so breastfeeding mothers should either avoid taking this medication or discontinue breastfeeding. If any unusual symptoms such as skin rash, difficulty breathing, severe headaches, indigestion, or bleeding occur while taking this medication, discontinue use immediately and consult a doctor. Prolonged use at high doses can affect kidney or liver function; therefore, regular examinations and medical monitoring are necessary. Before use, it is crucial to inform your doctor or pharmacist of any other medications currently being taken to check for possible interactions, particularly with blood pressure medications, diuretics, anticoagulants, etc. This drug may affect the fetus in early and mid-pregnancy, so women who are pregnant or planning to become pregnant should consult a healthcare professional before taking it.

Gastrointestinal bleeding, severe cardiovascular thrombotic reactions, myocardial infarction, stroke, bleeding of the stomach or intestines, ulcers, perforation, dyspepsia, abdominal bloating, heartburn, pain in the upper abdomen, diarrhea, constipation, loss of appetite, nausea, vomiting, abdominal pain, discomfort in the upper abdomen, esophagitis, esophageal stricture, exacerbation of diverticulitis, nonspecific hemorrhagic colitis, ulcerative colitis, Crohn's disease, peptic ulcer, gastrointestinal bleeding, perforation, blood in the stool, gastritis, pancreatitis, dry mouth, stomatitis, erythema multiforme, systemic lupus erythematosus, hair loss, angioedema, Stevens-Johnson syndrome, toxic epidermal necrolysis, eosinophilia, drug rash, acute generalized exanthematous pustulosis, rash, urticaria, itching, purpura, asthma attack, eczema, anaphylactic reaction, photosensitivity reaction, jaundice, elevated ALT, elevated AST, elevated ALP, liver dysfunction, hepatitis, rhinitis, bronchospasm, acute pneumonia, neglect, cancer infiltration, visual impairment, hearing loss, tinnitus, taste disturbance, fatigue, drowsiness, headache, dizziness, anxiety, restlessness, confusion, depression, aseptic meningitis, psychiatric symptoms, agitation, excitement, disorientation, reversible toxic amblyopia, hypotension, hypertension, palpitations, acute renal failure, oliguria, hematuria, increased urinary protein, elevated BUN, increased serum creatinine, hyperkalemia, decreased urine output, generalized edema, dyspnea, lethargy, renal papillary necrosis, nephrotic syndrome, interstitial nephritis, peripheral edema, acute pulmonary edema, fluid retention, hypertension, heart failure, Conis syndrome, decreased reproductive capability in women, periorbital edema, malaise, fever, epistaxis, exacerbation of inflammation, crying out, facial edema, dyspepsia, pruritus, anaphylactic shock, rash, diarrhea, vomiting

This medicine should be stored in a tightly sealed container to prevent exposure to air and moisture, ideally at a temperature between 1 and 30 degrees Celsius. Proper storage helps preserve the medication's efficacy and safety.

Appearance

White film-coated oblong tablet

Package unit

30 tablets/bottle, 300 tablets/bottle