Celecoxib Capsule 200mg (Celecoxib)

Adult dose

The minimum recommended dose of this drug should be adjusted according to the patient, and it may be administered with or without food. 1. Osteoarthritis (degenerative arthritis): Take celecoxib 200 mg once daily, or 100 mg twice daily in divided doses. 2. Rheumatoid arthritis: Take celecoxib 100 mg or 200 mg per dose twice daily. 3. Ankylosing spondylitis (AS): Administer celecoxib 200 mg once daily, or 100 mg twice daily in divided doses. If no effect is observed after 6 weeks, the dose may be increased up 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 celecoxib 400 mg, with an additional 200 mg on the first day of treatment if needed. From the second day of treatment, the recommended dose as needed is 200 mg per dose 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.

Individuals who drink a lot of alcohol daily should consult their doctor or pharmacist before taking this medication. Consuming this drug while drinking heavily may cause gastrointestinal bleeding. This medication can increase the risk of cardiovascular diseases. Serious thrombotic issues such as myocardial infarction or stroke may occur, so it should only be used for the shortest duration and at the lowest effective dose. Caution is required if there are gastrointestinal issues or in older individuals, as the risk of gastrointestinal bleeding, ulcers, and perforation increases with this medication. This drug should not be used in patients with specific allergies, severe impairment of liver or kidney function, active gastrointestinal bleeding, heart disease, or in pregnant or breastfeeding women. Patients with liver or kidney problems or a high risk of cardiovascular disease must use this medication carefully and undergo regular check-ups as directed by their physician. Dizziness or drowsiness may occur during treatment with this drug, so it is advisable to avoid driving or operating machinery. This medication is metabolized in the liver, so interactions may occur when taken with certain other drugs; therefore, consultation with a doctor or pharmacist is necessary. Pregnant women or those planning to become pregnant should avoid taking this medication, and it should be discontinued immediately if pregnancy is confirmed during use. Elderly patients may exhibit impaired liver, kidney, or heart function, requiring special attention and monitoring during treatment with this drug. Regular blood tests and liver and kidney function tests are required if taking this medication for a long period, and immediate consultation with healthcare providers is necessary if any unusual symptoms occur. In case of overdose, symptoms such as nausea, vomiting, drowsiness, gastrointestinal bleeding, etc. may present, and immediate medical attention is necessary. This medication is not recommended for use in children and adolescents, as safety and efficacy have not been established. When storing, keep it out of reach of children, and do not transfer it to another container.

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, confusional state, dizziness, muscle hypertonia, drowsiness, blurred vision, tinnitus, palpitations, congestive heart failure, arrhythmia, tachycardia, hypertension, flushing, cough, vomiting, abdominal pain, diarrhea, dyspepsia, abdominal distension, gastric ulcer, dental diseases, duodenal ulcer, esophageal ulcer, intestinal perforation, pancreatitis, elevated liver enzymes, itching, rash, urticaria, petechiae, angioedema, alopecia, bullous dermatitis, peripheral edema, facial edema, influenza-like illness, damage, taste disorder, albuminuria, cystitis, hematuria, dysuria, poliuria, kidney stones, urinary incontinence, urinary tract infection, visual blurring, cataract, conjunctivitis, eye pain, glaucoma, ocular hemorrhage, retinal artery or vein occlusion, increased serum creatinine, elevated β2-microglobulin, increased NAG, positive urinary hematuria, positive urinary protein, renal dysfunction, acute renal failure, interstitial nephritis, headache, migraine, neuralgia, neuropathy, sensory abnormalities, cerebral infarction, aseptic meningitis, ataxia, suicidal tendencies, anosmia, ageusia, back pain, allergic exacerbation, allergic reaction, weakness, chest pain, fluid retention, generalized edema, facial swelling, fatigue, lethargy, fever, facial flushing, influenza syndrome, pain, peripheral pain, sepsis, sudden death, anaphylaxis-like reaction, angioedema, loss of appetite, increased appetite, depression, irritability, drowsiness, lethal intracranial hemorrhage, hallucinations, exacerbation of epilepsy, 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, breast tenderness, menopausal symptoms, fibrocystic breast disease, chest neoplasm, 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, elevated ALP, positive urobilinogen, cholelithiasis, hepatitis, jaundice, liver failure, fulminant hepatitis, liver necrosis, increased blood sodium, increased blood potassium, elevated BUN, increased CPK, diabetes mellitus, hypercholesterolemia, hyperglycemia, hypokalemia, hyperkalemia, increased NPN, elevated creatinine, increased alkaline phosphatase, weight gain, increased LDH, hypoglycemia, hyponatremia, bursitis, arthralgia, arthrosis, skeletal abnormalities, myalgia, cervical dystonia, synovitis, tendinitis, myositis, leg cramps, fractures, tendon tears, pain in various parts, muscle stiffness, decreased hematocrit, increased hemoglobin, petechiae, epistaxis, thrombocytopathy, agranulocytosis, aplastic anemia, pancytopenia, leukopenia, angiolymphoid hyperplasia, contact dermatitis, injection site reactions, skin nodules, visual blurring, cataract, conjunctivitis, eye pain, glaucoma, ocular hemorrhage, retinal artery or vein occlusion, renal dysfunction, acute renal failure, interstitial nephritis, menstrual disorders, 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, liver necrosis, cholestasis, cholestatic hepatitis, jaundice, photosensitivity reactions, Stevens-Johnson syndrome, erythema multiforme, toxic epidermal necrolysis, drug eruption, acute generalized exanthematous pustulosis, exfoliative dermatitis, renal failure, hyponatremia, tubulointerstitial nephritis, nephrotic syndrome, minimal change disease glomerulonephritis, female infertility

Store this medication in an airtight container and at room temperature between 15 to 30 degrees Celsius. Proper storage helps maintain the drug's effectiveness and prevents degradation.

Appearance

Capsule filled with white to slightly yellow powder with white upper and lower parts.

Package unit

30 capsules/bottle, 100 capsules/bottle