Medication info
Tradiam Duo Tablet 2.5/500 mg

Tradiam Duo Tablet 2.5/500 mg

Prescription medicationTablet경구
Ingredient · strength
Linagliptin›2.5mg / 1 tabletMetformin Hydrochloride›500mg / 1 tablet
Manufacturer / importer
국제약품(주)
Appearance
Bright yellow, biconvex, oval film-coated tablet
Packaging
30 tablets/box[(6 tablets/PTP x 5 packs)]
Approval status
Active

MFDS item code 201802631 · Approved 2018.06.26 · Insurance code 643705520

Summary

Main use
Improvement of blood sugar control in type 2 diabetes
Who takes it
Adults
Adult dose
The dosage of this medication should be determined considering each ingredient's maximum recommended dosage of linagliptin 2.5 mg and metformin 1000 mg, not exceeding twice a day for each patient, based on their current treatment regimen, efficacy, and tolerability. This medication is administered twice a day with meals. 1. If currently not receiving treatment with metformin: Take this medication 2.5/500 mg, 1 tablet twice daily, up to 2.5/1000 mg.

Ingredients

Manufacturer
국제약품(주)

Efficacy & effects

Improvement of blood sugar control in type 2 diabetes

View approved original text

This medication helps improve blood sugar control in patients with type 2 diabetes by using linagliptin and metformin together. It is more effective when combined with dietary control and exercise therapy, contributing to stable management of blood sugar levels. Therefore, this medication is used for blood sugar control in patients with type 2 diabetes.

How to take

Adult dose

The dosage of this medication should be determined considering each ingredient's maximum recommended dosage of linagliptin 2.5 mg and metformin 1000 mg, not exceeding twice a day for each patient, based on their current treatment regimen, efficacy, and tolerability. This medication is administered twice a day with meals. 1. If currently not receiving treatment with metformin: Take this medication 2.5/500 mg, 1 tablet twice daily, up to 2.5/1000 mg.

Precautions

This medication is primarily used to control blood sugar levels. During the use of this medication, a rare complication called lactic acidosis may occur, so it is essential to check kidney and liver function before taking it. Patients with severely impaired kidney function or liver function problems, as well as those with acute illness or dehydration, should not take this medication. Additionally, it is not administered to patients with type 1 diabetes or those suffering from diabetic ketoacidosis or diabetic pre-coma. It is also recommended that pregnant or breastfeeding women refrain from using this medication. This medication may cause hypoglycemia, so blood sugar must be monitored closely, especially when taken with insulin or sulfonylureas. It is important to regularly check kidney function during the use of this medication to ensure no abnormalities occur. Acute pancreatitis or skin blistering disorders may appear, so if there are continuous abdominal pain or skin abnormalities, consult a doctor immediately. The risk of lactic acidosis increases when this medication is taken with alcohol, so alcohol consumption should be avoided. Additionally, during the use of this medication, it may be necessary to temporarily interrupt drug use before and after certain radiological tests. In elderly patients, the decline in kidney function is common, so kidney function should be monitored more closely during the use of this medication. The safety and efficacy of this medication have not been established in children, so it is not recommended for children under 10 years of age. If any unusual symptoms or discomfort occur during the use of the medication, it is important to consult a medical professional immediately.

Side effects and when to seek care immediately

Serious side effects

Lactic acidosis, urticaria, angioedema, pancreatitis, blistering dermatosis, liver function abnormalities (abnormal liver function tests, hepatitis, hepatic steatosis, acute cholangitis, acute cholecystitis, cholangitis), acute kidney injury, renal transplant failure, acute pyelonephritis, acute myocardial infarction, congestive heart failure, unstable angina, cardiac arrest, acute pneumonia, asthma, respiratory distress, voice disorders, acute cholangitis, acute cholecystitis, acute cholangitis, abdominal pain

Mild side effects

  • Nasopharyngitis
  • hypersensitivity
  • hypoglycemia
  • taste disturbances
  • cough
  • decreased appetite
  • diarrhea
  • constipation
  • nausea
  • vomiting
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  • abdominal pain
  • oral ulcer formation
  • abnormal liver function tests
  • hepatitis
  • itching
  • erythema
  • rash
  • severe arthralgia with disability
  • rhabdomyolysis
  • increased lipase
  • increased amylase
  • decreased and deficiency of vitamin B12
  • urticaria
  • angioedema
  • blistering dermatosis
  • constipation
  • pruritus
  • insomnia
  • depression
  • dizziness

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

Storage

This medication should be stored in a tightly closed container to protect it from air and moisture, preferably at room temperature between 1°C and 30°C. This storage helps maintain the medication's effectiveness and prevents degradation.

Appearance and packaging

Appearance

Bright yellow, biconvex, oval film-coated tablet

Package unit

30 tablets/box[(6 tablets/PTP x 5 packs)]

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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For anything that needs medical judgment, consult a doctor or pharmacist.

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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.