Celebrex Capsule 100 mg (Celecoxib)

Adult dose

The minimum recommended dose of this medication should be adjusted for each patient. It may be administered with or without food. ○ Adults 1. Osteoarthritis (degenerative arthritis) Take 200 mg of celecoxib once daily, or divide the dose into 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 divide the dose into 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 treatment, the recommended dose as needed is 200 mg twice daily. ○ Patients with hepatic impairment For patients with moderate hepatic impairment (Child-Pugh Class II), the dose should be reduced to approximately 50% of the recommended daily dose.

This medication should be discussed with a doctor or pharmacist if you are a regular consumer of three or more alcoholic beverages daily. This medication can cause gastrointestinal bleeding, so caution is needed. Due to the risk of cardiovascular problems, it may increase the chances of myocardial infarction or stroke, and should only be used at the lowest effective dose for the shortest duration. If cardiovascular symptoms appear, immediate medical attention is required, particularly for chest pain, shortness of breath, and slurred speech. Serious gastrointestinal issues such as perforation, ulcers, or bleeding may occur, so immediate treatment is necessary if symptoms like epigastric pain, indigestion, black stools, or hematemesis appear. Extra caution is needed for the elderly or those with a history of gastrointestinal disease; alternative treatments should be considered if there is a high risk of gastrointestinal bleeding. If allergic to this medication or having certain conditions, pregnant or breastfeeding women, and those with severe liver or kidney disease should not take it. Those with impaired liver or kidney function, asthma, heart failure, hypertension, edema, or dehydration should consult a doctor before use. Regular evaluation of liver and kidney function is necessary during treatment, and medical consultation is required if any abnormal symptoms occur. This medication can interact with other drugs, so if you are taking other medications, inform your doctor, especially when taking blood pressure medications, diuretics, anticoagulants, or antidepressants. Women who are pregnant or planning to become pregnant should avoid this medication and stop using it immediately upon confirmation of pregnancy. This medication can rarely cause severe skin reactions, so if symptoms like skin rashes, blisters, itching, or fever appear, discontinue use and seek medical assistance. Dizziness or drowsiness may occur, so care should be exercised when driving or operating machinery. Overdosage may lead to nausea, vomiting, drowsiness, or lethargy, requiring immediate medical treatment. This medication has not been established as safe for children, so it is not recommended for use in patients under 18 years of age. Elderly patients may have declining kidney and liver function, so careful monitoring is required during use. Keep this medication out of the reach of children, and do not store it in other containers.

Gastrointestinal bleeding, cardiovascular thrombotic reactions, myocardial infarction, stroke, perforation of the upper and lower gastrointestinal tract, ulcers, bleeding, bronchitis, sinusitis, upper respiratory tract infections, urinary tract infections, pharyngitis, rhinitis, anemia, thrombocytopenia, hypersensitivity, insomnia, anxiety, confusion, dizziness, muscle hypertonicity, drowsiness, blurred vision, tinnitus, palpitations, congestive heart failure, arrhythmia, tachycardia, hypertension, flushing, cough, vomiting, abdominal pain, diarrhea, dyspepsia, bloating, gastric ulcer, dental disease, duodenal ulcer, esophageal ulcer, intestinal perforation, pancreatitis, liver enzyme elevation, pruritus, rash, urticaria, petechiae, angioedema, alopecia, blistering dermatitis, peripheral edema, facial edema, influenza-like illness, damage, taste disturbance, albuminuria, cystitis, hematuria, dysuria, frequency of urination, nephrolithiasis, incontinence, urinary tract infections, visual disturbance, cataract, conjunctivitis, eye pain, glaucoma, retinal artery or vein occlusion, increased blood creatinine, increased β2-microglobulin, increased NAG, positive urine hematuria, positive urine protein, renal dysfunction, acute renal failure, interstitial nephritis, headache, migraine, neuralgia, neuropathy, sensory abnormalities, cerebral infarction, aseptic meningitis, ataxia, suicide, anosmia, ageusia, back pain, exacerbation of allergies, allergic reactions, weakness, chest pain, fluid retention, systemic edema, facial swelling, fatigue, lethargy, fever, facial flushing, influenza-like syndrome, pain, peripheral pain, sepsis, sudden death, anaphylaxis-like reaction, angioedema, loss of appetite, increased appetite, depression, neurogenic hypersensitivity, drowsiness, fatal intracranial hemorrhage, hallucinations, exacerbation of epilepsy, upper respiratory tract infections, sinusitis, pharyngitis, rhinitis, bronchospasm, exacerbated bronchospasm, dyspnea, laryngitis, pneumonia, nosebleeds, voice disorders, vesicular dermatitis, dermatitis, nail disorders, photosensitivity reactions, pruritus, erythematous rash, maculopapular rash, skin disorders, dry skin, increased sweating, erythema multiforme, exfoliative dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis, eczema, lipoma, allergic dermatitis, petechiae, dandruff, drug rash with eosinophilia and systemic symptoms, arrhythmia, ventricular hypertrophy, angina, unstable angina, coronary artery disorder, myocardial infarction, heart failure, palpitations, tachycardia, stroke, aortic valve insufficiency, hematoma, sinus bradycardia, syncope, ventricular fibrillation, pulmonary embolism, cerebrovascular accident, peripheral gangrene, thrombophlebitis, vasculitis, deep vein thrombosis, cerebral hemorrhage, solitary lesions, wound infections, gingivitis, herpes simplex, shingles, bacterial infections, fungal infections, soft tissue infections, viral infections, candidiasis, genital candidiasis, otitis media, breast tenderness, menopausal symptoms, fibrocystic breast disease, thoracic neoplasms, chest pain, dysmenorrhea, menstrual disorders, vaginal bleeding, vaginitis, prostate disorders, ovarian cysts, hearing loss, ear abnormalities, otalgia, hearing impairment, liver dysfunction, elevated ALT, elevated AST, increased γ-GTP, increased ALP, positive urine urobilinogen, cholelithiasis, hepatitis, jaundice, liver failure, fulminant hepatitis, hepatic necrosis, increased serum sodium, increased serum potassium, elevated BUN, elevated CPK, diabetes mellitus, hypercholesterolemia, hyperglycemia, hypokalemia, hyperkalemia, increased NPN, elevated creatinine, increased alkaline phosphatase, weight gain, elevated LDH, hypoglycemia, hyponatremia, bursitis, arthralgia, arthritis, skeletal abnormalities, myalgia, cervical tension syndrome, synovitis, tendinitis, myositis, leg cramps, fractures, tendon rupture, pain in the back, muscle stiffness, decreased hematocrit, increased hemoglobin, petechiae, nosebleeds, thrombocytopenic purpura, agranulocytosis, aplastic anemia, pancytopenia, leukopenia, polyarteritis, contact dermatitis, injection site reaction, skin nodules, visual disturbance, cataract, conjunctivitis, chest pain, anaphylactic reaction, hallucinations, cerebral hemorrhage, aseptic meningitis, loss of taste, loss of smell, conjunctivitis, vasculitis, pulmonary embolism, interstitial pneumonia, gastrointestinal bleeding, hepatitis, liver failure, fulminant hepatitis, hepatic necrosis, bile stasis, cholestatic hepatitis, jaundice, photosensitivity reactions, Stevens-Johnson syndrome, erythema multiforme, toxic epidermal necrolysis, drug rash, acute generalized exanthematous pustulosis, exfoliative dermatitis, acute renal failure, hyponatremia, tubulointerstitial nephritis, nephrotic syndrome, minimal change disease, menstrual disorders, female infertility, chest pain, lethargy, drowsiness, nausea, upper abdominal pain, hypertension, acute renal failure, respiratory depression, coma

This medication should be stored in a tightly sealed container to prevent air from entering, at room temperature between 15 degrees and 30 degrees Celsius. Proper storage ensures the maintenance of the drug's effectiveness.

Appearance

A white capsule with blue stripes filled with white to light yellow powder

Package unit

30 capsules/bottle, 100 capsules/bottle