Viewing nowDexlipen Tablet (Dexibuprofen D.C.)
Dexibuprofen D.C. 400mg
Tablet · Prescription medication
Aliko Pharmaceutical Co., Ltd.

MFDS item code 200709253 · Notified 2007.08.08 · Insurance code 656000090
Joint disorders (arthritis, etc.), inflammation following trauma or surgery, adjunctive treatment of infections
This medication is used to treat chronic inflammatory joint diseases such as chronic polyarthritis and rheumatoid arthritis, various joint issues known as arthropathy, ankylosing spondylitis, and pain-associated edema or inflammation occurring after trauma or surgery. Additionally, it serves as an adjunctive treatment to help with infections that present with inflammation, pain, and fever. Overall, this medication aids in improving patients' symptoms through the relief of inflammation and pain.
○ Adults: Administer 400 mg of dexibuprofen orally 2~3 times daily. However, do not exceed 1,200 mg of dexibuprofen per day.
This medicine should be discussed with a doctor or pharmacist before taking by people who regularly consume more than 3 glasses of alcohol daily, as it may cause gastrointestinal bleeding. This medicine may increase the risk of cardiovascular diseases. Serious cardiovascular issues such as myocardial infarction or stroke may occur; therefore, individuals with cardiovascular diseases or risk factors should exercise particular caution. This medication can cause serious gastrointestinal problems such as bleeding, ulcers, and perforation. The risk is particularly higher in elderly patients or those taking the medication for extended periods. Individuals with gastrointestinal conditions or bleeding, and severe liver, kidney, or heart diseases should not take this medication. Taking this medication with aspirin or other non-steroidal anti-inflammatory drugs may increase the risk of gastrointestinal bleeding, so it is best to avoid concurrent use. During breastfeeding, this medication might transfer into breast milk and cause adverse reactions in infants; therefore, breastfeeding should be discontinued or the drug should be stopped. This medication may cause dizziness or fatigue, so caution is needed when driving or operating machinery. Individuals with abnormal blood conditions, liver impairment, kidney impairment, hypertension, or heart failure should consult a doctor before taking this medication. If skin rashes, breathing difficulties, or severe gastrointestinal symptoms occur during treatment, discontinue use immediately and contact a doctor. Especially after the 6th month of pregnancy, this medication may be harmful to the fetus, so it should not be taken; women in early pregnancy or those planning to become pregnant should consult a specialist before use. This medication should be taken at the minimum effective dose and for the shortest duration necessary; regular health check-ups are required for long-term use. In case of overdose, even if there are no symptoms, seek urgent medical attention for appropriate treatment. This medication should be stored out of reach of children, kept away from direct sunlight, and stored in a cool, dry place.
Gastrointestinal bleeding, 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, diverticulitis exacerbation, nonspecific hemorrhagic colitis, ulcerative colitis, Crohn's disease, peptic ulcer, gastrointestinal bleeding, perforation, bloody stools, gastritis, pancreatitis, dry mouth, stomatitis, erythema multiforme, systemic lupus erythematosus, hair loss, angioedema, Stevens-Johnson syndrome, toxic epidermal necrolysis, eosinophilia, drug rash with systemic symptoms, acute generalized exanthematous pustulosis, rash, urticaria, itching, purpura, asthma attacks, eczema, anaphylaxis reactions, photosensitivity reactions, jaundice, elevated ALT, elevated AST, elevated ALP, abnormal liver function, hepatitis, rhinitis, bronchospasm, acute pneumonia, neglect, malignant neoplasm, visual impairment, hearing loss, tinnitus, taste disturbances, fatigue, drowsiness, headache, dizziness, anxiety, restlessness, confusion, depression, aseptic meningitis, psychiatric disorders, agitation, excitement, disorientation, reversible toxic amblyopia, hypotension, hypertension, palpitations, acute renal failure, oliguria, hematuria, proteinuria, elevated BUN, increased serum creatinine, hyperkalemia, decreased urine output, generalized edema, dyspnea, lethargy, necrosis of renal papillae, nephrotic syndrome, interstitial nephritis, peripheral edema, acute pulmonary edema, fluid retention, Conn's syndrome, reduced reproductive ability in women, periorbital edema, fatigue, fever, nosebleeds, exacerbation of inflammation, crying out, facial edema, dyspepsia, pruritus, anaphylactic shock, rash, diarrhea, vomiting
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. The storage temperature should be kept between 1 degree and 30 degrees Celsius.
White rectangular film-coated tablet
30 tablets/bottle, 300 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Aliko Pharmaceutical Co., Ltd.

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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.