Celebrex Capsule 100 mg (Celecoxib)

Adult dose

The minimum recommended dose of this medicine should be adjusted according to the patient and may be administered regardless of meals. Osteoarthritis (degenerative arthritis): Take celecoxib 200 mg once daily, or 100 mg twice daily. Rheumatoid arthritis: Take celecoxib 100 mg or 200 mg twice daily. 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 per day. If no effect is observed after 6 weeks of treatment with 400 mg per day, another treatment method should be considered. Acute pain and primary dysmenorrhea: The initial recommended 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, if 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 may increase the risk of gastrointestinal bleeding in individuals who consume alcohol in excess daily; therefore, consultation with a doctor or pharmacist is essential. The risk of cardiovascular issues such as heart attack or stroke may increase; hence, it should be taken at the lowest effective dose and for the shortest duration possible. There may be risks of ulcers or bleeding in the gastrointestinal tract, so careful monitoring is necessary, especially for the elderly or those with a history of gastrointestinal issues. Individuals allergic to this medication or with certain conditions, as well as women who are pregnant or breastfeeding, should not take it. Those with liver or kidney dysfunction or with asthma or cardiovascular disease should use this medication with caution and require regular monitoring. If symptoms such as chest pain, shortness of breath, severe abdominal pain, black stools, or vomiting blood occur during treatment, immediate consultation with healthcare providers is essential. This medication may interact with various drugs; therefore, you must inform your healthcare provider about any medications currently being taken. Women who are pregnant or planning to become pregnant should consult before use, as this medication may affect reproductive ability. The elderly should be cautious when taking this medication as they may have diminished kidney, liver, or heart function, and the risk of side effects may be higher, necessitating careful observation. This medication may cause dizziness or drowsiness during driving or operating machinery, so caution is warranted, and activities should be restricted if unusual symptoms occur. Regular blood tests and examinations of liver and kidney function should be conducted to monitor for abnormalities, especially with prolonged use. In case of overdose, symptoms such as vomiting, drowsiness, hypertension, and renal failure may occur, and immediate medical treatment is required. This medication should be kept out of reach of children and should not be transferred to other containers for safety.

Gastrointestinal bleeding, cardiovascular thrombotic events, 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 hypertonicity, 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, itching, rash, urticaria, petechiae, angioedema, alopecia, blistering dermatitis, peripheral edema, facial edema, influenza-like illness, injury, scleritis, contact dermatitis, injection site reaction, skin nodules, taste disturbance, albuminuria, cystitis, hematuria, dysuria, polyuria, kidney stones, urinary incontinence, urinary tract infections, visual disturbances, cataracts, conjunctivitis, eye pain, glaucoma, ocular hemorrhage, retinal artery or vein occlusion, increased serum creatinine, elevated β2-microglobulin, increased NAG, positive urine hematuria, positive urine protein, kidney dysfunction, acute renal failure, interstitial nephritis, anaphylactic reaction, hallucinations, intracerebral hemorrhage, aseptic meningitis, loss of taste, loss of smell, 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 exanthematous pustulosis, exfoliative dermatitis, acute renal failure, hyponatremia, tubular-interstitial nephritis, nephrotic syndrome, focal segmental glomerulosclerosis, menstrual disorders, chest pain, dyspepsia, diarrhea, headache, dizziness, constipation, gastric ulcer, urticaria, anemia, polydipsia, ulcerative stomatitis, gastritis, allergy, back pain, chest pain, hyperlipidemia, diabetes, weight gain, fractures, arthralgia, positive RA factor, herpes zoster, pneumonia, shortness of breath, elevated ALT, hearing loss

This medication should be stored in a tightly sealed container to prevent air and moisture intrusion, preferably at room temperature between 15 and 30 degrees Celsius. This helps maintain the medication's effectiveness over time.

Appearance

White to pale yellow powder filled capsule with blue stripes on the upper and lower parts.

Package unit

30 capsules per bottle, 100 capsules per bottle