Celebon Tablets 200 mg (Celecoxib)

Adult dose

The minimum recommended dose of this medication should be adjusted for each patient, and it may be administered with or without food. ○ Adults: 1. Osteoarthritis (degenerative joint disease): Take 200 mg of celecoxib once daily, or 100 mg twice daily. 2. Rheumatoid arthritis: Take 100 mg or 200 mg of celecoxib twice daily. 3. Ankylosing spondylitis (AS): Administer 200 mg of celecoxib once daily, or 100 mg twice daily. If no effect is observed after 6 weeks, the dose may be increased to 400 mg per day. If no effect is observed after 6 weeks of treatment with 400 mg per day, other treatment options should be considered. 4. Acute pain and primary dysmenorrhea: The recommended initial dose is 400 mg of celecoxib, with an additional 200 mg on the first day if needed. From the second day of administration, the recommended dose as needed is 200 mg twice daily. ○ Patients with hepatic impairment: In patients with moderate hepatic impairment (Child-Pugh Class II), the dose should be reduced to approximately 50% of the recommended daily dose.

This medication may cause gastrointestinal bleeding if taken by individuals who consume a lot of alcohol daily, so it is essential to consult a doctor or pharmacist. This medication may increase the risk of serious cardiovascular side effects, such as thrombotic reactions, myocardial infarction, and stroke, so it should be used at the minimum effective dose for the shortest duration. Serious gastrointestinal issues such as perforation, ulcers, and bleeding may occur, especially in elderly patients or those with a history of gastrointestinal disorders. This medication should not be prescribed to individuals with certain allergies, severe liver or kidney impairment, active peptic ulcers, cardiovascular diseases, pregnant or breastfeeding women. Patients with poor liver or kidney function, asthma, hypertension, heart failure, or diabetes should use this medication cautiously and require regular monitoring. Dizziness or drowsiness may occur during treatment, so it is advisable to avoid driving or operating machinery. This medication may interact with various drugs, so patients taking other medications must inform healthcare professionals. Women who are pregnant or planning to become pregnant should avoid taking this medication, and if pregnancy is confirmed during treatment, it should be discontinued immediately. Long-term use requires regular testing of liver and kidney function, as well as blood tests, to detect any abnormalities early on and to manage them promptly. Overdose may present symptoms such as nausea, vomiting, and lethargy, requiring immediate medical attention. Keep out of reach of children and do not store in another container.

Gastrointestinal bleeding, cardiovascular thrombotic reactions, myocardial infarction, stroke, perforation of the upper and lower gastrointestinal tract, ulcer, bleeding, bronchitis, sinusitis, upper respiratory infection, urinary tract infection, pharyngitis, rhinitis, anemia, thrombocytopenia, hypersensitivity, insomnia, anxiety, confusional state, dizziness, muscle tension, drowsiness, blurred vision, tinnitus, palpitations, congestive heart failure, arrhythmia, tachycardia, hypertension, flushing, cough, vomiting, abdominal pain, diarrhea, dyspepsia, distension, gastric ulcer, dental disease, duodenal ulcer, esophageal ulcer, intestinal perforation, pancreatitis, elevated liver enzymes, itching, rash, urticaria, petechiae, angioedema, alopecia, blistering dermatitis, peripheral edema, facial edema, influenza-like illness, injury, taste disturbance, albuminuria, cystitis, hematuria, dysuria, polyuria, kidney stones, urinary incontinence, visual blurring, cataract, conjunctivitis, eye pain, glaucoma, ocular hemorrhage, retinal artery or vein occlusion, increased serum creatinine, increased NAG, positive urine hematuria, positive urine protein, impaired renal function, acute kidney injury, interstitial nephritis, headache, leg cramps, tension hypertension, sensory decrease, migraine, neuralgia, neuropathy, sensory abnormalities, cerebral infarction, aseptic meningitis, ataxia, suicide, anosmia, ageusia, back pain, allergic exacerbation, allergic reaction, weakness, chest pain, fluid retention, systemic edema, facial edema, fatigue, lethargy, fever, facial flushing, influenza syndrome, pain, peripheral pain, sepsis, sudden death, anaphylaxis-like reaction, vasculitis, angioedema, hallucinations, epilepsy exacerbation, upper respiratory infection, shingles, wound infection, gingivitis, herpes simplex, herpes zoster, bacterial infection, fungal infection, soft tissue infection, viral infection, moniliasis, genital moniliasis, otitis media, breast tenderness, menopausal symptoms, fibrocystic breast disease, thoracic neoplasm, dysmenorrhea, menstrual disorders, vaginal bleeding, vaginitis, prostate disorders, ovarian cysts, hearing loss, ear abnormalities, ear pain, hearing impairment, liver dysfunction, increased ALT, increased AST, increased γ-GTP, increased ALP, positive urine urobilinogen, cholelithiasis, hepatitis, jaundice, liver failure, fulminant hepatitis, liver necrosis, increased sodium in the blood, increased potassium in the blood, increased BUN, increased CPK, diabetes, hypercholesterolemia, hyperglycemia, hypokalemia, hyperkalemia, increased NPN, increased creatinine, increased alkaline phosphatase, weight gain, loss of appetite, increased LDH, hypoglycemia, hyponatremia, synovial sac, arthralgia, arthropathy, skeletal anomalies, myalgia, cervical dystonia, synovitis, tendinitis, myositis, fractures, tendon rupture, back pain, muscle stiffness, decreased hematocrit, increased hemoglobin, petechiae, epistaxis, thrombocytopenic purpura, anemia, agranulocytosis, aplastic anemia, pancytopenia, leukopenia, vasculitis, contact dermatitis, injection site reaction, skin nodules, visual blurring, conjunctivitis, pulmonary embolism, interstitial pneumonia, gastrointestinal bleeding, hepatitis, photodermatosis, Stevens-Johnson syndrome, erythema multiforme, toxic epidermal necrolysis, drug rash, acute generalized exanthematous pustulosis, exfoliative dermatitis, acute kidney injury, hyponatremia, tubular interstitial nephritis, nephrotic syndrome, microvascular glomerulonephritis, female infertility, chest pain, anaphylactic reaction, hallucinations, cerebral hemorrhage, aseptic meningitis, loss of taste, loss of smell

This medication should be stored in a tightly sealed container to protect it from air and moisture. It is important to maintain a storage temperature between 1 to 30 degrees Celsius. This will help preserve the medication's effectiveness and prevent degradation.

Appearance

Yellow, oval-coated tablets

Package unit

100 tablets/bottle, 30 tablets/PTP (10 tablets/PTP * 3)