Medication info
Trip Em Duo Tablet 2.5/850 mg (Linagliptin, Metformin)

Trip Em Duo Tablet 2.5/850 mg (Linagliptin, Metformin)

Prescription medicationTablet경구
Ingredient · strength
Linagliptin Besylate›3.34mg / 1 tabletMetformin Hydrochloride›850mg / 1 tablet
Manufacturer / importer
(주)마더스제약
Appearance
Orange, biconvex, oval, film-coated tablet
Packaging
30 tablets/bottle, 60 tablets/bottle
Approval status
Active

MFDS item code 202401056 · Approved 2024.04.30

Summary

Main use
Improvement of blood sugar control in type 2 diabetes
Who takes it
Adults
Adult dose
The dosage of this drug is determined considering the current treatment regimen, efficacy, and tolerability of each patient, not exceeding the maximum recommended dosage of Linagliptin 2.5 mg (Linagliptin besilate 3.34 mg) and Metformin 1000 mg, administered twice daily. This drug is taken twice daily with meals. 1. If currently not treated with Metformin: Initial dosage of this drug is 2.5/500 mg.

Ingredients

Manufacturer
(주)마더스제약

Efficacy & effects

Improvement of blood sugar control in type 2 diabetes

View approved original text

This drug is used to assist in the blood sugar control of patients with type 2 diabetes by using Linagliptin and Metformin together. It helps manage blood sugar levels effectively while following a dietary regimen and exercise. This contributes to the prevention of complications related to diabetes and maintaining a healthy life. Therefore, this drug is used to improve blood sugar control in conjunction with dietary and exercise therapy.

How to take

Adult dose

The dosage of this drug is determined considering the current treatment regimen, efficacy, and tolerability of each patient, not exceeding the maximum recommended dosage of Linagliptin 2.5 mg (Linagliptin besilate 3.34 mg) and Metformin 1000 mg, administered twice daily. This drug is taken twice daily with meals. 1. If currently not treated with Metformin: Initial dosage of this drug is 2.5/500 mg.

Precautions

This drug is used for the treatment of diabetes. However, it should not be administered to patients with poor kidney function or severe liver dysfunction. Rare but serious side effects such as lactic acidosis may occur, so kidney and liver function should be checked periodically. Also, patients with unstable heart function or cardiovascular diseases such as acute myocardial infarction should avoid using this drug. Pregnant or breastfeeding women should not take this drug. This drug has a risk of hypoglycemia, so when used in conjunction with insulin or sulfonylurea class medications, blood sugar conditions should be carefully monitored. If symptoms such as abdominal pain, severe muscle pain, difficulty breathing, or weakness occur during use, consult a doctor immediately. Rare side effects such as acute pancreatitis or bullous pemphigoid with skin blisters may occur, so if such symptoms arise, discontinue the medication and consult a specialist. This drug may lower vitamin B12 levels, so regular testing of vitamin B12 levels is necessary during long-term use. Furthermore, caution should be taken when taken with other medications that can affect kidney function, and dosage adjustment may be required as needed. In special situations such as surgery or radiation examinations, the use of this drug should be temporarily suspended, and resumption should occur only after kidney function stabilizes. Elderly patients are at higher risk of reduced kidney function, so kidney function should be monitored frequently, and appropriate dosage adjustments should be made when using this drug. The safety and efficacy of this drug in children have not been fully established, thus it is not recommended for children under 10 years old. Lastly, this drug should be stored out of reach of children and kept away from moisture.

Side effects and when to seek care immediately

Serious side effects

Urticaria, angioedema, lactic acidosis, pancreatitis, bullous pemphigoid, liver dysfunction (abnormal liver function tests, hepatitis), angina, acute myocardial infarction, unstable angina, congestive heart failure, cardiac arrest, pneumonia, difficulty breathing, asthma, acute kidney injury, end-stage renal disease, acute cholangitis, acute cholecystitis, cholangitis, erythema, severe allergic reactions, severe skin adverse reactions, respiratory problems, liver impairment (jaundice), serious neurological.

Mild side effects

  • Nasopharyngitis
  • hypersensitivity
  • angioedema
  • hypoglycemia
  • taste disorder
  • cough
  • decreased appetite
  • diarrhea
  • constipation
  • nausea
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  • vomiting
  • abdominal pain
  • mouth ulcer formation
  • abnormal liver function tests
  • hepatitis
  • pruritus
  • erythema
  • rash
  • severe and disabling arthralgia
  • rhabdomyolysis
  • increased lipase
  • increased amylase
  • decreased and deficiency of vitamin B12
  • nosebleed
  • oropharyngeal pain
  • speech disorder
  • wet cough
  • runny nose
  • anxiety
  • insomnia.

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

Storage

This drug may be sensitive to air or moisture, so it must be stored in a tightly sealed container. It is advisable to maintain a storage temperature between 1 to 30 degrees Celsius (room temperature). This will help maintain the effectiveness and safety of the drug for an extended period.

Appearance and packaging

Appearance

Orange, biconvex, oval, 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.

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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.