Medication info
Trinam 5/1000 mg Extended-Release Tablet (Linagliptin, Metformin)

Trinam 5/1000 mg Extended-Release Tablet (Linagliptin, Metformin)

Prescription medicationTablet경구
Ingredient · strength
Linagliptin Besylate›6.67mg / 1 tabletMetformin Hydrochloride›1000mg / 1 tablet
Manufacturer / importer
대웅바이오(주)
Appearance
This drug is a yellow oval-shaped extended-release film-coated tablet.
Packaging
30 tablets/bottle, 60 tablets/bottle
Approval status
Active

MFDS item code 202401579 · Approved 2024.06.28 · Insurance code 694004290

Summary

Main use
Improvement of blood sugar control in type 2 diabetes
Who takes it
Adults
Adult dose
The dosage of this medication is determined within the limits of the maximum recommended daily doses for each ingredient: Linagliptin 5 mg (Linagliptin benzoate 6.67 mg) and extended-release Metformin hydrochloride 2000 mg. It is taken once daily with the evening meal. For the 5/1000 mg extended-release tablet, take 1 tablet once daily. For the 2.5/1000 mg extended-release tablet, take 2 tablets once daily.

Ingredients

Manufacturer
대웅바이오(주)

Efficacy & effects

Improvement of blood sugar control in type 2 diabetes

View approved original text

This medication helps in the control of blood sugar levels in patients with type 2 diabetes by combining linagliptin and metformin. It is administered as an adjunct to dietary and exercise therapy, enabling effective management of blood glucose levels. This helps improve blood sugar control and assists in the management of diabetes.

How to take

Adult dose

The dosage of this medication is determined within the limits of the maximum recommended daily doses for each ingredient: Linagliptin 5 mg (Linagliptin benzoate 6.67 mg) and extended-release Metformin hydrochloride 2000 mg. It is taken once daily with the evening meal. For the 5/1000 mg extended-release tablet, take 1 tablet once daily. For the 2.5/1000 mg extended-release tablet, take 2 tablets once daily.

Precautions

This drug is used for the treatment of diabetes and helps lower blood sugar. However, it may rarely cause a serious condition called lactic acidosis, warranting caution. It should not be used in patients with poor kidney function, liver dysfunction, or in acute conditions such as acute myocardial infarction or severe infections. Patients with allergies to any component of this drug or those with type 1 diabetes should also avoid its use. There is a risk of hypoglycemia, so blood glucose changes must be carefully monitored when used with insulin or sulfonylureas. In situations where renal function is impaired, temporary discontinuation of this drug may be necessary. Additionally, acute pancreatitis or blistering skin conditions may develop, so consult a physician immediately if symptoms occur. This drug may lower vitamin B12 levels, necessitating regular blood tests during prolonged use. Alcohol consumption can increase the risk of lactic acidosis and should be avoided. Use during pregnancy or breastfeeding should be avoided, and patients planning pregnancy should consult a physician. Elderly patients have a higher risk of kidney function deterioration and require dosage adjustments and regular kidney function tests. In situations that could impact kidney function, such as surgery or radiological examinations, administration of this drug should be temporarily suspended. This medication must be swallowed whole and should not be chewed or crushed. Be aware that there may be drug interactions, so inform your physician or pharmacist of any other medications you are taking. Overdose may cause gastrointestinal disorders or lactic acidosis, requiring immediate medical attention. Store this medication away from children's reach, keep it in a dry place, and store it in the original container.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (angioedema), chest tightness, difficulty breathing, lactic acidosis, pancreatitis, bullous pemphigoid, abnormal liver function (including hepatitis and jaundice), acute myocardial infarction, angina, cardiac arrest, acute kidney injury, kidney transplant failure, severe allergic reactions, severe skin reactions, serious neurological symptoms (severe headache, seizures, confusion, visual disturbances, paralysis), severe edema or urination abnormalities (decreased urine output, systemic severe

Mild side effects

  • Pharyngitis
  • taste disturbance
  • cough
  • loss of appetite
  • diarrhea
  • constipation
  • nausea
  • vomiting
  • abdominal pain
  • oral ulcer
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  • abnormal liver function
  • hepatitis
  • itching
  • erythema
  • rash
  • severe arthralgia with disability
  • rhabdomyolysis
  • increased lipid-cleaving enzymes
  • increased amylase
  • abnormal vitamin B12 absorption test
  • angioedema
  • hypoglycemia
  • increased serum triglycerides
  • increased serum creatinine
  • increased serum potassium
  • decreased hemoglobin
  • fatty liver
  • hypertension

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

Storage

This drug is sensitive to air and moisture; therefore, it should be stored in a sealed container. It is crucial to maintain a storage temperature between 1 and 30 degrees Celsius. This helps ensure the drug's effectiveness is safely preserved for an extended period.

Appearance and packaging

Appearance

This drug is a yellow oval-shaped extended-release film-coated tablet.

Package unit

30 tablets/bottle, 60 tablets/bottle

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.