Celecoxib Capsule 200 Milligrams (Celecoxib)

Adult dose

The minimum recommended dose of this medication should be adjusted for each patient, and it may be taken regardless of meals. ○ 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, another treatment should be considered. 4. Acute pain and primary dysmenorrhea: The recommended initial dose is 400 mg of celecoxib; if needed, an additional 200 mg may be administered on the first day of treatment. 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 should be discussed with a doctor or pharmacist before use by people who drink alcohol excessively on a daily basis, as it may cause stomach bleeding. Additionally, this medication may increase the risk of heart or vascular problems, so it should only be used at the lowest possible dose for the shortest duration. Symptoms should be closely monitored, and immediate action should be taken if symptoms such as chest pain or shortness of breath occur, even if there is no history of cardiovascular disease. It may also affect the stomach, leading to serious problems such as stomach ulcers, bleeding, or perforation, so caution is needed, particularly for older adults or those with a history of gastrointestinal disorders. If symptoms such as epigastric pain, indigestion, black stools, or vomiting blood arise during treatment, a hospital visit is required immediately. This medication may cause various side effects, such as allergic reactions, liver or kidney dysfunction, and skin rashes, so any abnormal symptoms should be reported immediately. Women who are pregnant or may become pregnant, as well as nursing mothers, should not use this medication. Patients with severe heart disease, active gastric ulcers, or inflammatory bowel disease should also avoid use. This medication can interact with various other medications, so if any other treatments are being taken, medical personnel should be informed. Older adults may be at higher risk for decreased kidney and liver function, requiring careful monitoring. Regular blood tests and liver and kidney function checks should be done during treatment, and if any abnormal findings arise, usage should be discontinued. If dizziness or drowsiness occurs after taking this medication, driving or operating machinery should be avoided. This medication may harm the fetus during pregnancy, so it should not be used during pregnancy, and women planning to become pregnant should exercise caution. This medication can affect various body systems, including the gastrointestinal, cardiovascular, renal, hepatic, and skin, so it is important to closely observe symptoms before and after use.

Gastrointestinal bleeding, cardiovascular thrombotic events, myocardial infarction, stroke, perforation of the upper and lower gastrointestinal tract, ulcer, bleeding, bronchitis, sinusitis, upper respiratory tract infection, urinary tract infection, pharyngitis, rhinitis, anemia, thrombocytopenia, hypersensitivity, insomnia, anxiety, confusion, dizziness, muscle hypertonia, drowsiness, blurred vision, tinnitus, palpitations, congestive heart failure, arrhythmia, tachycardia, hypertension, flushing, cough, vomiting, abdominal pain, diarrhea, dyspepsia, bloating, gastric ulcer, dental diseases, duodenal ulcer, esophageal ulcer, intestinal perforation, pancreatitis, elevated liver enzymes, pruritus, rash, urticaria, petechiae, angioedema, alopecia, vesicular dermatitis, peripheral edema, facial edema, influenza-like illness, injury, taste disturbance, albuminuria, cystitis, hematuria, dysuria, polyuria, nephrolithiasis, urinary incontinence, urinary tract infection, blurred vision, cataract, conjunctivitis, eye pain, glaucoma, ocular hemorrhage, retinal arterial or venous occlusion, increased serum creatinine, increased β2-microglobulin, increased NAG, positive urine hematuria, positive urine protein, renal dysfunction, acute renal failure, interstitial nephritis, increased serum sodium, increased serum potassium, increased BUN, increased CPK, diabetes, hypercholesterolemia, hyperglycemia, hypokalemia, hyperkalemia, increased NPN, increased creatinine, increased alkaline phosphatase, weight gain, decreased appetite, increased LDH, hypoglycemia, hyponatremia, synovial sac, arthralgia, arthrosis, skeletal abnormalities, myalgia, cervical stiffness, synovitis, tendinitis, myositis, leg cramps, fractures, tendon rupture, pain in areas such as back, muscle rigidity, decreased hematocrit, increased hemoglobin, petechiae, nosebleeds, thrombocytopathy, agranulocytosis, aplastic anemia, pancytopenia, leukopenia, eosinophilic esophagitis, contact dermatitis, injection site reactions, skin nodules, headache, dizziness, constipation, thirst, ulcerative stomatitis, gastritis, allergy, low back pain, chest pain, hyperlipidemia, weight gain, fractures, arthralgia, positive RA factor, shingles, pneumonia, shortness of breath, elevated ALT, hearing loss, anaphylactic reaction, hallucinations, cerebral hemorrhage, aseptic meningitis, taste loss, smell loss, vasculitis, pulmonary embolism, interstitial pneumonia, hepatitis, liver failure, fulminant hepatitis, liver necrosis, cholestasis, cholestatic hepatitis, jaundice, photosensitivity reaction, Stevens-Johnson syndrome, erythema multiforme, toxic epidermal necrolysis, drug rash, acute generalized pustular dermatitis, exfoliative dermatitis, acute renal failure, hyponatremia, tubulointerstitial nephritis, nephrotic syndrome, minimal change disease, menstrual disorders, female infertility

This medication should be stored in a tightly sealed container to prevent air and moisture from entering, and it is best kept in a cool place between 15 to 30 degrees Celsius. Storing it this way helps maintain the effectiveness of the medication and ensures safe use.

Appearance

A white capsule filled with a white to light yellow powder with a yellow band at both ends.

Package unit

Bottle - 30 capsules/bottle, Bottle - 100 capsules/bottle