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Dexibuprofen D.C. 400mg
Tablet · Prescription medication
Celix Co., Ltd.

MFDS item code 200708961 · Notified 2007.08.01
Treatment of joint disorders (e.g., arthritis); adjunctive treatment of infections; relief of pain and inflammation after trauma or surgery
This medication is used for chronic inflammatory joint diseases such as chronic polyarthritis, rheumatoid arthritis, and ankylosing spondylitis. It is also effective for relieving pain and swelling caused by joint disease and trauma or surgery. This medication can assist in treating infections accompanied by inflammation, pain, and fever. In summary, this medication is used to suppress inflammation and alleviate pain.
○ Adults: Administer 400 mg of dexibuprofen orally 2~3 times daily. Do not exceed 1,200 mg of dexibuprofen daily.
This medication may pose a risk of gastrointestinal bleeding if taken regularly by individuals who consume more than 3 alcoholic drinks daily; consultation with a physician or pharmacist is essential. This medication may increase the risk of cardiovascular diseases, so special caution is warranted for patients with known cardiovascular issues or risk factors. Elderly patients or those with a history of gastrointestinal disorders should use this medication cautiously as it can cause serious gastrointestinal issues such as bleeding, ulcers, or perforation. Individuals with a history of gastrointestinal ulcers or bleeding, severe liver or kidney disease, severe heart failure, hypertension, or asthma should not take this medication. The risk of gastrointestinal bleeding may increase when used in conjunction with aspirin or other non-steroidal anti-inflammatory drugs, so co-administration is not recommended. During breastfeeding, this medication can transfer into breast milk and cause adverse reactions in infants, so breastfeeding should be discontinued or the medication halted. Dizziness or fatigue may occur while taking this medication, requiring caution when driving or operating machinery. Patients with abnormal blood, liver, or kidney function should consult a physician, undergo regular testing, and immediately stop taking the medication if unusual symptoms arise. Particularly after the sixth month of pregnancy, this medication may harm the fetus, so its use should be avoided; women planning to become pregnant should also consult beforehand. If severe allergic reactions, skin rashes, breathing difficulties, or severe gastrointestinal symptoms occur while taking this medication, immediate cessation and consultation with healthcare professionals are required. This medication should be used at the minimum effective dose for the shortest duration, with regular health status checks required for long-term use. In the case of overdose, even if there are no apparent symptoms, prompt medical attention is advised for appropriate treatment. This medication should be kept out of reach of children, stored 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, aggravated diverticulitis, 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, acute generalized pustular psoriasis, rash, urticaria, itching, purpura, asthma attacks, eczema, anaphylactic reaction, photosensitivity reaction, jaundice, elevated ALT, elevated AST, elevated ALP, liver dysfunction, hepatitis, rhinitis, bronchospasm, acute pneumonia, neglect, cancer infiltration, visual disturbances, hearing loss, tinnitus, dysgeusia, fatigue, drowsiness, headache, dizziness, anxiety, restlessness, confusion, depression, aseptic meningitis, mental disturbance, agitation, excitement, disorientation, reversible toxic encephalopathy, hypotension, hypertension, palpitations, acute renal failure, oliguria, hematuria, proteinuria, 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, Conn's syndrome, reduced reproductive capacity in women, periorbital edema, malaise, fever, nosebleed, exacerbation of inflammation, agitation, facial swelling, dyspepsia, pruritus, anaphylactic shock, rash, headache
Not everyone experiences these, and they can vary from person to person.
Store this medication in a tightly closed container to protect it from air and moisture. The recommended storage temperature is between 1 to 30 degrees Celsius at room temperature. This helps to maintain the medication's effectiveness and safety over time.
Pink, oblong film-coated tablets
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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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.