Celebit Capsule 100mg (Celecoxib)

Adult dose

The minimum recommended dose of this medicine should be adjusted according to the patient and may be administered regardless of meals. ○ Adults 1. Osteoarthritis (degenerative arthritis) Take 200 mg of celecoxib once daily, or divide the dose into 100 mg per dose twice daily. 2. Rheumatoid arthritis Take 100 mg or 200 mg of celecoxib per dose twice daily. 3. Ankylosing spondylitis (AS) Administer 200 mg of celecoxib once daily, or divide the dose into 100 mg per dose 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 method should be considered. 4. Acute pain and primary dysmenorrhea The initial recommended dose is 400 mg of celecoxib, 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 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.

This medication should be consulted with a doctor or pharmacist if you frequently consume daily amounts of alcohol, as it may pose a risk of gastrointestinal bleeding. Anyone with heart or vascular issues or at risk of cardiovascular disease should use this medication for the shortest duration possible at minimal doses, and seek immediate medical advice if symptoms arise. Individuals with a history of gastrointestinal ulcers or bleeding must be cautious, as serious issues such as gastrointestinal perforation, ulcers, and bleeding may occur with this medication. Elderly patients and those with a history of gastrointestinal disorders should be especially careful. This medication should not be used by those with specific allergic reactions, severe liver or kidney dysfunction, active gastrointestinal bleeding, a history of heart failure or cardiovascular diseases, or women who are pregnant or breastfeeding. Those with liver or kidney issues or asthma, heart failure, hypertension, edema, dehydration, or the elderly should take this medication under careful observation. Various adverse reactions such as dyspepsia, headaches, dizziness, skin rashes, hypertension, edema, abdominal pain, and vomiting may occur during use, and immediate medical consultation is necessary if symptoms worsen or new symptoms appear. Since this medication is metabolized in the liver, dose adjustments may be needed when taken with other medications that affect liver function, and caution is required with possible interactions with blood pressure medications, diuretics, anticoagulants, and antidepressants. Women who are pregnant or planning to become pregnant should avoid taking this medication, as it may affect the fetus, and those who are breastfeeding should also discontinue use or stop breastfeeding. Children and adolescents should preferably avoid using this medication due to the lack of established safety and efficacy. Elderly patients should have their doses adjusted and be closely monitored due to potential declines in kidney and liver function. For those taking this medication long-term, regular blood tests and assessments of liver and kidney function are necessary, and if any abnormal signs are observed, discontinuation may be required. Dizziness or drowsiness may occur during use, so it is safer to avoid driving or operating machinery. This medication can cause allergic reactions or serious skin reactions, so if symptoms such as rashes, blisters, fever, or itching occur, immediate discontinuation and medical consultation are necessary. In cases of overdose, symptoms such as nausea, vomiting, drowsiness, gastrointestinal bleeding, and renal failure may appear, requiring immediate treatment at a medical institution. When storing, keep this medication in a tightly sealed container away from children's reach 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, confusion, dizziness, muscle hypertonia, drowsiness, blurred vision, tinnitus, palpitations, congestive heart failure, arrhythmias, tachycardia, hypertension, flushing, cough, vomiting, abdominal pain, diarrhea, dyspepsia, bloating, gastric ulcers, dental diseases, duodenal ulcers, esophageal ulcers, intestinal perforation, pancreatitis, elevated liver enzymes, itching, rash, urticaria, petechiae, angioedema, alopecia, vesicular dermatitis, peripheral edema, facial edema, influenza-like illnesses, injuries, headaches, constipation, thirst, ulcerative stomatitis, gastritis, allergies, back pain, chest pain, hyperlipidemia, diabetes, weight gain, fractures, arthralgia, RA factor positive, shingles, pneumonia, dyspnea, elevated ALT, hearing loss, anaphylactic reactions, hallucinations, cerebral hemorrhage, aseptic meningitis, loss of taste, loss of smell, conjunctivitis, vasculitis, pulmonary embolism, interstitial pneumonia, hepatitis, liver failure, fulminant hepatitis, hepatic necrosis, cholestasis, cholestatic hepatitis, jaundice, photosensitivity reactions, Stevens-Johnson syndrome, erythema multiforme, toxic epidermal necrolysis, drug rashes, acute generalized exanthematous pustulosis, exfoliative dermatitis, acute kidney failure, hyponatremia, tubulointerstitial nephritis, nephrotic syndrome, minimal lesion glomerulonephritis, menstrual disorders, female infertility, chest pain, weakness, fluid retention, generalized edema, facial edema, fatigue, malaise, fever, facial flushing, influenza-like syndrome, pain, peripheral pain, sepsis, sudden death, anaphylactoid reactions, angioedema, loss of appetite, increased appetite, depression, neuroexcitability, drowsiness, fatal intracranial hemorrhage, hallucinations, exacerbation of epilepsy, upper respiratory tract infections, sinusitis, pharyngitis, rhinitis, bronchospasm, worsening bronchospasm, laryngitis, pneumonia, nosebleeds, voice disorders, vesicular dermatitis, dermatitis, nail diseases, photosensitivity reactions, pruritus, erythematous rashes, erythematous papular rashes, dermatological diseases, dry skin, increased sweating, erythema multiforme, exfoliative dermatitis, mucous membrane syndrome, toxic epidermal necrolysis, petechiae, dandruff, drug rashes associated with eosinophilia and systemic symptoms, decreased hematocrit, increased hemoglobin, petechiae, nosebleeds, thrombocytopathy, agranulocytosis, aplastic anemia, pancytopenia, leukopenia, granulomatous inflammation, contact dermatitis, injection site reactions, dermatological nodules, taste distortion, albuminuria, cystitis, hematuria, dysuria, polyuria, nephrolithiasis, urinary incontinence, urinary tract infections, blurred vision, cataracts, conjunctivitis, eye pain, glaucoma, ocular hemorrhage, retinal artery or vein occlusion, increased serum creatinine, increased β2-microglobulin, increased NAG, positive urine hematuria, positive urine protein, renal dysfunction, acute kidney failure, interstitial nephritis

This medication should be stored in a tightly sealed container that allows air to circulate, maintaining a temperature between 15 to 30 degrees Celsius. Proper storage will help preserve the medication's efficacy and prevent degradation.

Appearance

A white capsule filled with powder that is white to pale yellow, with a blue line on the top and bottom.

Package unit

30 capsules/bottle, 100 capsules/bottle