Medication info

InjenTa Duo Tablets 2.5/500 mg

Prescription medicationTablet경구Expired
Ingredient · strength
Linagliptin›2.5mg / 1 tabletMetformin Hydrochloride›500mg / 1 tablet
Manufacturer / importer
(주)비보존제약
Appearance
Biconvex oval film-coated tablet in bright yellow color
Packaging
60 tablets/box [10 tablets/PTP Χ 6]
Approval status
Expired

MFDS item code 202001551 · Approved 2020.03.05

This product's status changed to Expired on 2025.03.05. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Improvement of blood sugar control in adults with type 2 diabetes
Who takes it
Adults
Adult dose
This medication is administered twice daily with meals. 1. If currently not being treated with metformin: The initial dose is to take this drug 2.5/500 mg twice daily, one tablet at a time, and can be increased to 2.5/1000 mg twice daily, one tablet at a time. 2. When switching from a combination therapy of linagliptin and metformin: Patients previously taking linagliptin and metformin at the same dosage are to start this medication at the same dosage.

Ingredients

Manufacturer
(주)비보존제약

Efficacy & effects

Improvement of blood sugar control in adults with type 2 diabetes

  • Difficulty in controlling blood sugar in patients with type 2 diabetes
View approved original text

This drug is mainly used to help control blood sugar levels in adult patients with type 2 diabetes. It is administered as an adjunct to dietary therapy and exercise, and can be used when it is difficult to control blood sugar levels alone in patients who have not previously received diabetes medication. Additionally, it can replace the combination of linagliptin and metformin or be co-administered with insulin when the combination of insulin and metformin is insufficient. It can also be used in conjunction with this medication when blood sugar control is inadequate even with the maximum dose of metformin and empagliflozin. Thus, it is used to effectively control blood sugar in combination with various therapies tailored to the patient's condition.

How to take

Adult dose

This medication is administered twice daily with meals. 1. If currently not being treated with metformin: The initial dose is to take this drug 2.5/500 mg twice daily, one tablet at a time, and can be increased to 2.5/1000 mg twice daily, one tablet at a time. 2. When switching from a combination therapy of linagliptin and metformin: Patients previously taking linagliptin and metformin at the same dosage are to start this medication at the same dosage.

Precautions

This medication may cause a rare but serious side effect known as lactic acidosis, so caution is needed. Lactic acidosis occurs when there is a buildup of lactic acid in the body, which can be life-threatening if not treated. Individuals allergic to this drug's active ingredients or any components should not take it. Type 1 diabetes patients, those with lactic acidosis or diabetic ketoacidosis, and people with severe renal impairment should also avoid this medication. Avoid this drug if you have conditions that can affect kidney function, such as severe infections, dehydration, or acute myocardial infarction. Patients with impaired liver function or gastrointestinal disorders should refrain from using this drug. Pregnant or breastfeeding women are advised not to use this drug. When using this medication in conjunction with other blood glucose-lowering agents, caution is necessary due to the risk of hypoglycemia. Particularly when combined with sulfonylureas or insulin, the risk of hypoglycemia may increase and dose adjustments may be needed. The usage and dosage of this drug should be adjusted based on kidney function, and regular kidney function tests are necessary. This medication may need to be temporarily discontinued before and after acute illnesses or surgeries, so follow your doctor's instructions. If you experience sudden abdominal pain, muscle weakness, difficulty breathing, or lethargy while taking this drug, go to the hospital immediately. This drug may lower vitamin B12 levels, thus vitamin B12 testing may be required during long-term use. It is advisable to avoid alcohol consumption while taking this medication, as alcohol can increase the risk of lactic acidosis. If iodine contrast media is to be used during radiological examinations, this drug should be discontinued before and after the test and kidney function must be checked. The elderly should take this medication with particular caution due to the potential for reduced kidney function, and dosage adjustments and regular testing are needed. This medication is not recommended for children or adolescents as safety and effectiveness have not been sufficiently proven. If skin blisters or rashes occur while taking this medication, consult your doctor immediately. In case of overdose, the risk of lactic acidosis increases, so it is essential to adhere to the prescribed dosage, and immediate medical attention is required in the event of overdose.

Side effects and when to seek care immediately

Serious side effects

Urticaria, angioedema, lactic acidosis, blistering similar to pemphigus, acute pancreatitis, liver function abnormalities (abnormal liver function tests, hepatitis), angina, acute myocardial infarction, unstable angina, cardiac arrest, heart failure (congestive heart failure), difficulty breathing, asthma, pneumonia, cerebral infarction, acute kidney injury, end-stage renal disease, fever, discomfort in the chest, headache, confusion of consciousness, visual disturbances, paralysis, hypoglycemia (when linagliptin/metformin is combined with sulfonylureas)

Mild side effects

Nasopharyngitis, various gastrointestinal disorders (loss of appetite, diarrhea, constipation, nausea, vomiting, abdominal pain, stomatitis), reduced and deficient vitamin B12 levels, taste disturbances, cough, pruritus, rash, increased blood triglycerides, increased amylase, angioedema, indigestion, anxiety, depression, dizziness, drowsiness, itching, lightheadedness, headache, insomnia, fever, pain, discomfort in the chest, weakness, chest pain, voice disorders, runny nose,

Not everyone experiences these, and they can vary from person to person.

Storage

This medication is sensitive to air and moisture, so it should be stored in a tightly sealed container. The recommended storage temperature is between 1 degree and 30 degrees Celsius at room temperature. This will help maintain the drug's effectiveness longer.

Appearance and packaging

Appearance

Biconvex oval film-coated tablet in bright yellow color

Package unit

60 tablets/box [10 tablets/PTP Χ 6]

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

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.

Questions about this medicine

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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.