Nailak Combination Tablet

Adult dose

Adults: Take 1 tablet twice daily. This medicine may be taken with or without food. Swallow this medicine whole; do not crush or split it. ○ Patients with hepatic impairment Use of this medicine is not recommended when initiating treatment in patients with hepatic impairment who require a dose reduction (see 5. General precautions under Precautions for use).

This medication may cause gastrointestinal bleeding if taken by individuals who regularly consume more than three glasses of alcohol daily; it is necessary to consult a doctor or pharmacist. This medication may increase the risk of cardiovascular diseases, potentially leading to serious thrombotic events such as myocardial infarction or stroke. It should be taken at the minimum effective dose and for the shortest period possible while closely monitoring for cardiovascular symptoms. It may affect the gastrointestinal tract, potentially causing gastrointestinal perforation, ulcers, and bleeding. Therefore, special caution is needed for the elderly or those with a history of gastrointestinal diseases. If symptoms such as epigastric pain, indigestion, black stools, or vomiting blood occur, immediate consultation with medical professionals is required. This medication is not to be administered to individuals with specific allergic reactions, severe cardiovascular diseases, severely impaired liver or kidney functions, or active gastric ulcers. Pregnant or breastfeeding individuals, or women who may become pregnant, should not take this medication, and if pregnancy is confirmed during treatment, it should be discontinued immediately. Patients with liver or kidney impairment, hypertension, heart failure, asthma, or diabetes should exercise special caution while taking this medication. This medication may cause various adverse reactions such as liver dysfunction, kidney impairment, blood disorders, skin rashes, etc.; any unusual symptoms should be reported to a healthcare provider immediately. Potential symptoms may include headache, dizziness, indigestion, skin itchiness, edema, etc., and in severe cases, treatment should be discontinued. This medication may interact with other drugs, so patients currently on other medications should consult with their doctor or pharmacist. Particularly, careful monitoring is necessary when used with antihypertensives, diuretics, anticoagulants, antidepressants, antiepileptics, etc. Regular blood tests, liver function tests, and kidney function tests are recommended to check for abnormalities during treatment. Dizziness or drowsiness may occur after taking this medication, thus driving or operating machinery should be avoided. In case of overdose, symptoms such as nausea, vomiting, lethargy, high blood pressure, and acute renal failure may occur, warranting an immediate visit to the hospital. The safety and efficacy of this medication have not been established for children, and elderly patients should have dosage adjustments and monitoring due to potential kidney and liver function decline. Store this medication out of reach of children and do not transfer it to another container.

Gastrointestinal bleeding, cardiovascular thromboembolic response, myocardial infarction, stroke, perforation of the upper and lower gastrointestinal tract, ulcer, bleeding, dyspepsia, nausea, upper abdominal pain, constipation, diarrhea, dry mouth, esophageal pain, stomatitis, infection, COVID-19, acute pyelonephritis, facial edema, insertion site pain, peripheral edema, fever, pruritus, psoriasis, rash, skin swelling, alanine aminotransferase elevation, aspartate aminotransferase elevation, increased blood pressure, elevated serum uric acid, gamma-glutamyltransferase elevation, arthralgia, low back pain, coccygodynia, flank pain, headache, carpal tunnel syndrome, lymphadenopathy, cholelithiasis, bronchitis, sinusitis, upper respiratory tract 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, distension, gastric ulcer, dental disease, duodenal ulcer, esophageal ulcer, intestinal perforation, pancreatitis, itching, urticaria, angioedema, alopecia, vesicular dermatitis, peripheral edema, influenza-like illness, injury, decreased hematocrit, increased hemoglobin, nosebleed, thrombocytopathy, agranulocytosis, aplastic anemia, pancytopenia, leukopenia, eosinophilic infiltration, contact dermatitis, skin nodules, taste disturbance, albuminuria, cystitis, hematuria, dysuria, pollakiuria, nephrolithiasis, urinary incontinence, blurred vision, cataract, conjunctivitis, eye pain, glaucoma, ocular hemorrhage, retinal artery or vein occlusion, elevated serum creatinine, increased β2-microglobulin, increased NAG, positive urine hematuria, positive urine protein, renal dysfunction, acute renal failure, interstitial nephritis, menstrual disorder, chest pain, insomnia, constipation, gastritis, abdominal cramps, gastroesophageal reflux disease, epigastric discomfort, non-food-related epigastric pain, headache, dizziness, drowsiness, heartburn, dry mouth, nausea, diarrhea, weakness, hypertriglyceridemia, hypercholesterolemia, Transaminitis, elevated ALT, elevated AST, itching, leukopenia, neutropenia, chest discomfort

This medication should be stored in a tightly sealed container to avoid exposure to air and moisture. It is advisable to keep it at room temperature between 1 and 30 degrees Celsius.

Appearance

Yellow rectangular film-coated tablet consisting of two layers

Package unit

30 tablets/bottle, 300 tablets/bottle