Uniilaplus Tablets

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 can cause gastrointestinal bleeding if taken by individuals who regularly consume more than three glasses of alcohol a day; therefore, consulting a doctor or pharmacist is essential. This medication can increase serious cardiovascular risks such as cardiovascular thrombotic events, myocardial infarction, and stroke. These risks may increase with the dose and duration of use, so it is crucial to take the lowest possible dose for the shortest duration. This medication can lead to serious adverse reactions such as gastrointestinal perforation, ulcers, and bleeding, and the risk is greater in elderly patients or those with a history of gastrointestinal disease; if gastrointestinal symptoms occur during use, it is necessary to consult healthcare professionals immediately. This medication should not be administered to individuals with certain allergy histories or severe cardiovascular, liver, or kidney conditions, those with active peptic ulcers or inflammatory bowel disease, or women who are pregnant or breastfeeding. Patients with impaired liver or kidney function, hypertension, heart failure, asthma, elderly patients, etc., should take extra caution when using this medication, requiring regular monitoring of health status. Common side effects may include dyspepsia, headache, skin rash, swelling, and hypertension, and in case of severe skin reactions, the medication should be stopped immediately and healthcare professionals should be consulted. This medication may interact with other drugs; patients taking any other medications must inform their doctor or pharmacist, especially if taking blood pressure medications, anticoagulants, antidepressants, or diuretics. Women who are pregnant or planning to become pregnant should avoid taking this medication, and breastfeeding women should consult a specialist before use. The safety and efficacy of this medication have not been confirmed for children and adolescents, so it is advisable not to use it in individuals under 18 years of age. Elderly patients may be at risk of impaired kidney, liver, or heart function when taking this medication; therefore, careful monitoring by a doctor before and after administration is necessary. Patients on long-term medication should undergo regular blood tests as well as liver and kidney function tests to check for abnormalities; if any abnormal findings are discovered, use should be discontinued immediately. In case of overdose, symptoms may include lethargy, drowsiness, nausea, vomiting, and upper abdominal pain; immediate medical attention should be sought for appropriate treatment. This medication should be kept out of reach of children and should not be transferred to another container.

Gastrointestinal bleeding, cardiovascular thrombotic reactions, myocardial infarction, stroke, perforation of the upper and lower gastrointestinal tract, ulcers, bleeding, dyspepsia, nausea, upper abdominal pain, constipation, diarrhea, dry mouth, esophageal pain, stomatitis, acute pyelonephritis, facial swelling, pain at the site of insertion, peripheral edema, fever, pruritus, psoriasis, rash, skin swelling, elevated alanine aminotransferase, elevated aspartate aminotransferase, increased blood pressure, elevated blood uric acid, increased gamma-glutamyltransferase, arthralgia, back pain, coccygodynia, flank pain, headache, carpal tunnel syndrome, lymphadenopathy, cholelithiasis, palpitations, congestive heart failure, arrhythmia, tachycardia, hypertension, flushing, cough, vomiting, abdominal pain, bloating, gastric ulcer, dental disease, duodenal ulcer, esophageal ulcer, bowel perforation, pancreatitis, itching, urticaria, angioedema, alopecia, vesicular dermatitis, peripheral edema, facial swelling, influenza-like illness, injury, anemia, thrombocytopenia, insomnia, anxiety, confusion, dizziness, muscle hypertonia, drowsiness, blurred vision, tinnitus, congestive heart failure, arrhythmia, tachycardia, hypertension, flushing, cough, gastrointestinal bleeding, elevated liver enzymes, vesicular dermatitis, petechiae, angioedema, alopecia, vesicular dermatitis, Stevens-Johnson syndrome, toxic epidermal necrolysis, drug rash, acute generalized exanthematous pustulosis, exfoliative dermatitis, peripheral edema, chest pain, fluid retention, generalized edema, facial swelling, fatigue, malaise, fever, facial flushing, influenza syndrome, pain, peripheral pain, sepsis, sudden death, anaphylactic-like reaction, angioedema, hallucinations, exacerbation of epilepsy, upper respiratory infection, sinusitis, pharyngitis, rhinitis, bronchitis, bronchospasm, exacerbation of bronchospasm, dyspnea, laryngitis, pneumonia, nosebleed, voice disorders, vesicular dermatitis, petechiae, alopecia, dermatitis, nail disorders, photosensitivity reactions, itchiness, erythematous rash, maculopapular eruption, skin disorders, dry skin, increased sweating, urticaria, erythema multiforme, exfoliative dermatitis, mucosal syndrome, toxic epidermal necrolysis, drug rash accompanied by eosinophilia and systemic symptoms, vasculitis, pulmonary embolism, interstitial pneumonia, hepatitis, hepatic failure, fulminant hepatitis, hepatic necrosis, cholestasis, cholestatic hepatitis, jaundice, acute renal failure, tubulointerstitial nephritis, nephrotic syndrome, minimal change glomerulonephritis, menstrual disorders, female infertility, chest pain, heartburn, dry mouth, nausea, diarrhea, weakness, hypertriglyceridemia, hypercholesterolemia, transaminitis, increased ALT, increased AST, itching, leukopenia, neutropenia, discomfort in the chest, blurred vision, constipation, gastric ulcer, urticaria, anemia, thirst, ulcerative stomatitis, gastritis, allergy, low back pain, chest pain, hyperlipidemia, diabetes, weight gain, fractures, arthralgia, RA factor positive, herpes zoster, pneumonia, dyspnea, elevated ALT, hearing loss, headache, dizziness, gastritis, gastroesophageal reflux, peripheral edema, dizziness, drowsiness, gastrointestinal bleeding, anaphylactic reaction, hallucinations, cerebral hemorrhage, aseptic meningitis, loss of taste, loss of smell, conjunctivitis, vasculitis, pulmonary embolism, interstitial pneumonia, hepatitis, hepatic failure, fulminant hepatitis, hepatic 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, tubulointerstitial nephritis, nephrotic syndrome, minimal change glomerulonephritis, menstrual disorders, female infertility, chest pain, heartburn, dry mouth, nausea, diarrhea, weakness, hypertriglyceridemia, hypercholesterolemia, transaminitis, increased ALT, increased AST, itching, leukopenia, neutropenia, discomfort in the chest, blurred vision

This medication is sensitive to air and moisture, so it must be stored in a tightly closed container. It is important to maintain a storage temperature between 1 degree and 30 degrees Celsius at room temperature. This will help preserve the efficacy of the medication for a longer period.

Appearance

A yellow oblong film-coated tablet consisting of two layers

Package unit

30 tablets/bottle, 300 tablets/bottle