TDS Celecoxib Capsule 200 Milligrams

Adult dose

The minimum recommended dose of this medicine should be adjusted according to the patient, and it may be administered with or without food. ○ Adults: 1. Osteoarthritis (degenerative arthritis): Administer celecoxib 200 mg once daily, or 100 mg twice daily. 2. Rheumatoid arthritis: Administer celecoxib 100 mg or 200 mg twice daily. 3. Ankylosing spondylitis (AS): Administer celecoxib 200 mg once daily, or 100 mg twice daily. If no effect is observed after 6 weeks, the dose may be increased to 400 mg daily. If no effect is observed after 6 weeks of treatment with 400 mg daily, another treatment option should be considered. 4. Acute pain and primary dysmenorrhea: The recommended initial dose is celecoxib 400 mg, with an additional 200 mg on the first day of treatment if needed. From the second day onward, the recommended dose, if 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 in those who drink large amounts of alcohol daily; therefore, consultation with a doctor or pharmacist is required. It may affect heart or brain health, and individuals at risk of cardiovascular disease should use the minimum effective dose for the shortest duration necessary. Those with ulcers or bleeding in the stomach should be cautious as serious gastrointestinal issues could arise while using this medication. Individuals with allergic reactions, especially to sulfonamides, aspirin, or other non-steroidal anti-inflammatory drugs, should not take this medication. Those with severe liver or kidney dysfunction, weak heart function, or women who are pregnant or breastfeeding should also avoid using this drug. Occasionally, side effects such as headache, dyspepsia, skin rash, elevated blood pressure, edema, and dizziness may occur, and any unusual symptoms should be reported to medical personnel immediately. This medication may interact with other drugs; individuals taking blood pressure medications, diuretics, anticoagulants, or antidepressants should consult their doctor. Women who are pregnant or planning to become pregnant should avoid using this medication as it may affect the fetus, and caution is also needed during breastfeeding. Elderly patients may have reduced kidney and liver function, so they should be monitored more carefully when using this medication. It is important to have regular blood tests and liver and kidney function tests during the use of this medication to check for any abnormalities. In cases of overdose, symptoms such as nausea, vomiting, drowsiness, and gastrointestinal bleeding may occur, so the prescribed dosage must be strictly followed, and in case of unusual symptoms, immediate medical attention should be sought. Keep this medication out of reach of children, and do not transfer it to other containers for safety.

Gastrointestinal bleeding, cardiovascular thrombotic reactions, myocardial infarction, stroke, upper and lower gastrointestinal perforation, ulcer, bleeding, bronchitis, sinusitis, upper respiratory tract infection, urinary tract infection, pharyngitis, rhinitis, anemia, thrombocytopenia, hypersensitivity, insomnia, anxiety, delirium, dizziness, muscle tension, sedation, 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, itching, rash, urticaria, petechiae, angioedema, alopecia, vesicular dermatitis, peripheral edema, facial edema, influenza-like illness, injury, taste disturbance, albuminuria, cystitis, hematuria, dysuria, polyuria, kidney stones, urinary incontinence, urinary tract infection, blurred vision, cataract, conjunctivitis, eye pain, glaucoma, ocular hemorrhage, retinal artery or vein occlusion, elevated serum creatinine, increased β2-microglobulin, increased NAG, positive urine hematuria, positive urine protein, renal dysfunction, acute renal failure, interstitial nephritis, headache, leg cramps, tension, sensory reduction, migraine, neuralgia, neuropathy, sensory abnormalities, cerebral infarction, aseptic meningitis, ataxia, suicide, anosmia, ageusia, back pain, exacerbation of allergies, allergic reaction, weakness, chest pain, fluid retention, generalized edema, facial swelling, fatigue, lethargy, fever, facial flushing, influenza-like syndrome, pain, peripheral pain, sepsis, sudden death, anaphylaxis-like reactions, angioedema, insomnia, loss of appetite, increased appetite, depression, neuro-irritability, drowsiness, fatal intracranial hemorrhage, hallucinations, convulsions, upper respiratory tract infection, shingles, wound infection, gingivitis, herpes simplex, herpes zoster, bacterial infection, fungal infection, soft tissue infection, viral infection, moniliasis, genital moniliasis, otitis media, mastalgia, menopausal symptoms, fibrocystic disease of the breast, thoracic neoplasm, chest pain, dysmenorrhea, menstrual disorders, vaginal bleeding, vaginitis, prostatic disorders, ovarian cysts, hearing loss, ear abnormalities, otalgia, hearing impairment, liver dysfunction, elevated ALT, elevated AST, increased γ-GTP, increased ALP, positive urine bilirubin, cholelithiasis, hepatitis, jaundice, liver failure, fulminant hepatitis, hepatic necrosis, elevated serum sodium, elevated serum potassium, increased BUN, increased CPK, diabetes, hypercholesterolemia, hyperglycemia, hypokalemia, hyperkalemia, elevated NPN, increased creatinine, increased alkaline phosphatase, weight gain, loss of appetite, increased LDH, hypoglycemia, hyponatremia, synovial sac, arthralgia, arthritis, skeletal abnormalities, myalgia, cervical tension, synovitis, tendinitis, myositis, fracture, tendon rupture, pain in the back, muscle stiffness, decreased hematocrit, increased hemoglobin, petechiae, epistaxis, thrombocytopathy, anemia, thrombocytopenia, agranulocytosis, aplastic anemia, pancytopenia, leukopenia, polyarthritis, contact dermatitis, injection site reactions, skin nodules, blurred vision, cataract, conjunctivitis, eye pain, glaucoma, ocular hemorrhage, retinal artery or vein occlusion, elevated serum creatinine, increased β2-microglobulin, increased NAG, positive urine hematuria, positive urine protein, renal dysfunction, acute renal failure, interstitial nephritis, anaphylaxis reactions, hallucinations, cerebral hemorrhage, aseptic meningitis, loss of taste, loss of smell, conjunctivitis, vasculitis, pulmonary embolism, interstitial pneumonia, gastrointestinal bleeding, hepatitis, photosensitivity reactions, Stevens-Johnson syndrome, erythema multiforme, toxic epidermal necrolysis, drug rash, acute generalized exanthematous pustulosis, exfoliative dermatitis, acute renal failure, hyponatremia, tubular interstitial nephritis, nephrotic syndrome, minimal change disease glomerulonephritis, menstrual disorders, female infertility, chest pain, lethargy, drowsiness, nausea, vomiting, epigastric pain, hypertension, acute renal failure, respiratory depression, coma

This medication should be stored in a tightly sealed container to prevent air and moisture from entering. It is also recommended to store the medication at room temperature between 15°C to 30°C, avoiding extremes of hot or cold.

Appearance

A white capsule filled with a powder that is white to light yellow.

Package unit

30 capsules/bottle, 100 capsules/bottle