Linagliptin Metformin Tablets 2.5/1000 mg
Linagliptin 2.5mg · Metformin Hydrochloride 1000mg
Prescription medication · Combination
Hanmi Pharmaceutical Co., Ltd.
MFDS item code 201801859 · Approved 2018.04.30
Improvement of blood glucose control in adult type 2 diabetes
This medication is used in conjunction with dietary and exercise therapy to improve blood glucose control in patients with type 2 diabetes. It may be administered when previous treatment with diabetes medications has not been received, or when adequate blood glucose control is not achieved with monotherapy. Additionally, it is used when blood glucose control is insufficient with either monotherapy using metformin or combination therapy with other medications (such as sulfonylureas, insulin, empagliflozin, etc.). This medication effectively regulates blood glucose by replacing or complementing various combination therapies. Therefore, it is an important therapeutic agent that helps in controlling blood glucose levels in patients with type 2 diabetes.
The dosage of this medication is determined based on the maximum recommended doses of each component, which are 2.5 mg of linagliptin and 1000 mg of metformin, not exceeding twice daily, considering the patient's current treatment regimen, efficacy, and tolerability. This medication is to be taken twice daily with meals. 1. If the patient is not currently being treated with metformin: the initial dose is this medication 2.5/500 mg, taken twice daily, 1 tablet per dose.
This medication is used to treat type 2 diabetes and helps to control blood glucose levels. This medication may cause serious side effects such as lactic acidosis, so it should not be used in patients with poor kidney function, heart disease, or liver dysfunction. In particular, patients with an allergy to any of the components included in this medication or those with type 1 diabetes, pregnant or breastfeeding women should not take it. Due to the risk of hypoglycemia, caution is required when using this medication with insulin or sulfonylureas, and doses of other medications may be adjusted as necessary. If kidney function is impaired, it is essential to check kidney function before using this medicine and monitor it regularly. This medication should be temporarily discontinued during surgery or radiological examinations, and it can be restarted after kidney function has recovered. Skin conditions like acute pancreatitis or bullous pemphigoid may occur, and any abdominal pain or skin abnormalities during use should be reported to a doctor immediately. Gastrointestinal disturbances such as diarrhea, abdominal pain, nausea, and vomiting may occur during the use of this medication, but most improve naturally over time. As vitamin B12 levels may decrease, regular blood tests are recommended during long-term use to check levels. This medication may interact with other drugs, so inform your doctor or pharmacist of any other medications you are taking. Women who are pregnant or planning to become pregnant should avoid taking this medication and use other treatments for blood glucose control. Elderly patients should have their kidney function checked frequently, as decreased kidney function is common, and it is advisable to start with the lowest dose. It is recommended not to use this medication in children under 10 years of age, as safety and efficacy have not been established. In case of overdose, serious side effects such as lactic acidosis may occur, so the dosage must be strictly adhered to, and if any unusual symptoms appear, immediate medical attention should be sought. This medication should be stored in a cool, dry place away from moisture and direct sunlight, out of reach of children.
Urticaria, angioedema, lactic acidosis, pancreatitis, bullous pemphigoid, chest tightness, difficulty breathing, asthma attack, yellowing of skin or eyes (jaundice), liver dysfunction, sudden and severe headache, seizures, confusion, visual disturbances, paralysis, significant decrease in urine output, severe swelling of the body and hypertension, angina pectoris, acute myocardial infarction, unstable angina, cardiac arrest, congestive heart failure, heart failure, acute
Not everyone experiences these, and they can vary from person to person.
This medication is sensitive to air and moisture and should be stored in a tightly closed container. The recommended storage temperature is between 1 to 30 degrees Celsius. Proper storage will help maintain the effectiveness of the medication.
Light pink, double-convex, oval film-coated tablet
60 tablets (10 tablets/PTP packaging x 6 units)
Even with the same ingredient, strength, dosage form and how it is taken can differ.
Linagliptin 2.5mg · Metformin Hydrochloride 1000mg
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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.