Enseco Capsule 200 mg (Celecoxib)

Adult dose

The minimum recommended dose of this drug should be adjusted for each patient, and it 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 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, a dose of up to 400 mg daily may be administered. If no effect is observed after 6 weeks of treatment with 400 mg daily, another treatment should be considered. 4. Acute pain and primary dysmenorrhea : The recommended initial 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 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 if taken by individuals who consume large amounts of alcohol daily, so it is essential to consult a doctor or pharmacist. Due to the risk of heart or vascular-related problems, it should be used at the lowest possible dose for the shortest duration. Individuals with a history of ulcers or gastrointestinal bleeding need to take caution when using this medication, and should seek medical attention immediately if symptoms such as stomach pain or indigestion occur. Those with allergic reactions or hypersensitivity to specific medications should avoid taking this medicine, especially asthma patients and those with severe heart, liver, or kidney diseases. Pregnant or nursing women should not take this medication, and women who could become pregnant should also refrain from its use. Patients with weakened liver or kidney function, and those with cardiovascular diseases such as hypertension or heart failure should ensure to consult a doctor before taking this medication and use it cautiously. This medication may interact with other drugs, so if currently taking any medications, inform the doctor or pharmacist, especially when taking blood pressure medications, diuretics, anticoagulants, antidepressants, etc. Dizziness or drowsiness may occur during treatment, so it is advisable to avoid driving or operating machinery. If taken for an extended period, regular blood tests and checks of liver and kidney function should be conducted to monitor for abnormalities. In case of overdose, symptoms such as nausea, vomiting, drowsiness, or gastrointestinal bleeding may occur, and immediate hospital treatment should be sought. Keep out of reach of children and do not transfer to other containers for safety.

Gastrointestinal bleeding, cardiovascular thrombotic reaction, myocardial infarction, stroke, perforation of the upper and lower gastrointestinal tract, ulcer, bleeding, bronchitis, sinusitis, upper respiratory infection, urinary tract infection, pharyngitis, rhinitis, anemia, thrombocytopenia, hypersensitivity, insomnia, anxiety, confusion, dizziness, muscle tension, drowsiness, 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, elevated liver enzymes, itching, rash, urticaria, petechiae, angioedema, alopecia, blistering dermatitis, peripheral edema, facial swelling, influenza-like illness, injury, taste disturbance, albuminuria, cystitis, hematuria, dysuria, polyuria, nephrolithiasis, 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 urine hematuria, positive urine protein, renal impairment, acute renal failure, interstitial nephritis, headache, migraine, neuralgia, neuropathy, paresthesia, cerebral infarction, aseptic meningitis, ataxia, suicide, loss of smell, loss of taste, exacerbation of allergy, allergic reaction, weakness, chest pain, fluid retention, systemic edema, facial edema, fatigue, malaise, fever, facial flushing, influenza-like syndrome, pain, peripheral pain, sepsis, sudden death, anaphylactic-like reaction, angioedema, vasculitis, pulmonary embolism, interstitial pneumonia, hepatitis, liver failure, fulminant hepatitis, hepatic necrosis, phototoxic reactions, Stevens-Johnson syndrome, erythema multiforme, toxic epidermal necrolysis, drug rash, acute generalized exanthematic pustulosis, exfoliative dermatitis, fixed drug eruption, fixed drug rash, hyponatremia, tubular interstitial nephritis, nephrotic syndrome, minimal change disease, menstrual disorders, chest pain, dyspepsia, diarrhea, urticaria, anemia, thirst, ulcerative stomatitis, gastritis, allergy, back pain, hyperlipidemia, diabetes, weight gain, fracture, arthralgia, RA factor positive, shingles, pneumonia, dyspnea, elevated ALT, hearing loss

This medication should be stored in a tightly closed container to prevent exposure to air, and kept at room temperature between 15 to 30 degrees. This storage condition helps maintain the medication's efficacy and safety.

Appearance

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

Package unit

30 capsules/bottle, 100 capsules/bottle