Dexidel Tablet 400mg (Dexibuprofen D.C.)

Adult dose

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

This medication should be consulted with a doctor or pharmacist if taken by individuals who regularly consume more than 3 drinks a day, as it may cause serious side effects such as gastrointestinal bleeding. This medication may increase the risk of cardiovascular diseases; therefore, individuals with a history of heart disease or stroke or those with risk factors should be cautious, and immediate medical attention is required if cardiovascular symptoms occur during use. Severe gastrointestinal issues such as gastrointestinal bleeding, ulcers, and perforations may occur, so individuals with a history of gastrointestinal diseases or the elderly should exercise particular caution when using this medication. This medication contains certain colorants, and special care should be taken if allergic to these ingredients. Individuals with gastrointestinal ulcers, bleeding, severe liver or kidney dysfunction, severe hypertension, or a history of asthma should not take this medication. Taking this medication with aspirin or other non-steroidal anti-inflammatory drugs may increase the risk of side effects; therefore, co-administration is not recommended. During the use of this medication, breastfeeding should be discontinued or discussed with a doctor; dizziness or fatigue may occur, and caution is needed when driving or operating machinery. Individuals with blood abnormalities, liver or kidney diseases, hypertension, heart failure, allergies, the elderly, or children should consult a healthcare professional before taking this medication. This medication may interact with various drugs, so if taking other medications, be sure to inform a healthcare professional. In case of serious allergic reactions, skin rashes, breathing difficulties, blood abnormalities, liver function abnormalities, or other unusual symptoms, discontinue use immediately and consult a healthcare professional. It should be avoided during pregnancy, especially after the sixth month, as it may pose a risk to the fetus; if taken during pregnancy, thorough consultation with a doctor is necessary. In case of overdose, seek appropriate treatment at a medical facility immediately. This medication should be stored out of reach of children, away from direct sunlight, and in a cool, dry place.

Gastrointestinal bleeding, serious cardiovascular thrombotic reactions, myocardial infarction, stroke, bleeding from the stomach or intestines, ulcers, perforation, dyspepsia, abdominal distension, heartburn, upper abdominal pain, diarrhea, constipation, loss of appetite, nausea, vomiting, abdominal pain, gastric discomfort, esophagitis, esophageal stricture, exacerbation of diverticulitis, nonspecific hemorrhagic colitis, ulcerative colitis, Crohn's disease, peptic ulcer gastrointestinal bleeding, perforation, bloody stool, gastritis, pancreatitis, thirst, stomatitis, erythema multiforme, systemic lupus erythematosus, hair loss, angioedema, Stevens-Johnson syndrome, toxic epidermal necrolysis, eosinophilia, drug rash with systemic symptoms, acute generalized pustular psoriasis, rash, urticaria, itching, purpura, asthma attacks, eczema, anaphylactic reactions, photosensitivity reactions, jaundice, elevated ALT, elevated AST, elevated ALP, liver dysfunction, hepatitis, rhinitis, bronchospasm, acute pneumonia, neglect, malignancy, visual disturbances, hearing loss, tinnitus, taste disturbances, fatigue, drowsiness, headache, dizziness, anxiety, restlessness, confusion, depression, aseptic meningitis, psychiatric disorders, agitation, excitement, disorientation, reversible toxic myopathy, hypotension, hypertension, palpitations, acute renal failure, oliguria, hematuria, increased proteinuria, elevated BUN, elevated serum creatinine, hyperkalemia, decreased urine output, generalized edema, dyspnea, lethargy, renal papillary necrosis, nephrotic syndrome, interstitial nephritis, peripheral edema, acute pulmonary edema, fluid retention, decreased reproductive capacity in women, periorbital edema, malaise, fever, nosebleeds, exacerbation of inflammation, crying, facial swelling, dyspepsia, pruritus, anaphylactic shock, rash, diarrhea, vomiting

This medication may be sensitive to air and moisture; therefore, it should be stored in a tightly closed container. Additionally, it is advisable to store the medicine at room temperature between 1 and 30 degrees Celsius. This will help maintain the medication's effectiveness.

Appearance

Pink rectangular film-coated tablet

Package unit

30T, 300T / Bottle