Medication info
Tragliflozin Duo Tablet 2.5/850mg

Tragliflozin Duo Tablet 2.5/850mg

Prescription medicationTablet경구
Ingredient · strength
Linagliptin›2.5mg / 1 tabletMetformin Hydrochloride›850mg / 1 tablet
Manufacturer / importer
신일제약(주)
Appearance
Bright orange, bilaterally convex oval film-coated tablet
Packaging
10 tablets/bottle, 30 tablets/bottle, 60 tablets/bottle, 100 tablets/bottle, 200 tablets/bottle, 30 tablets/box (10 tablets/PTP x 3)
Approval status
Active

MFDS item code 201902170 · Approved 2019.04.09 · Insurance code 653806290

Summary

Main use
Improvement of blood sugar control in type 2 diabetes
Who takes it
Adults
Adult dose
This medication is administered twice daily with meals. To minimize gastrointestinal side effects associated with metformin, dose increases should be gradual. 1. For patients not currently treated with metformin: Start with an initial dose of this medication at 2.5/500 mg twice daily, one tablet per dose, with the option to increase to 2.5/1000 mg twice daily, one tablet per dose. 2. For metformin users:

Ingredients

Manufacturer
신일제약(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 combining linagliptin and metformin. It acts as an adjunct to diet and exercise therapy to effectively manage blood glucose levels. This contributes to the prevention of complications and the maintenance of a healthy life.

How to take

Adult dose

This medication is administered twice daily with meals. To minimize gastrointestinal side effects associated with metformin, dose increases should be gradual. 1. For patients not currently treated with metformin: Start with an initial dose of this medication at 2.5/500 mg twice daily, one tablet per dose, with the option to increase to 2.5/1000 mg twice daily, one tablet per dose. 2. For metformin users:

Precautions

This medication helps control blood sugar levels. However, during this treatment, there is a risk of serious side effects such as lactic acidosis. Lactic acidosis is a condition caused by excessive accumulation of lactate in the body, which can be life-threatening if not treated immediately. This medication should not be administered to patients with certain conditions. For example, individuals allergic to the components of this drug, those with type 1 diabetes, patients with severe renal impairment, acute heart diseases, liver dysfunction, pregnant or breastfeeding women should not take this medication. When using it in conjunction with other hypoglycemic agents that pose a risk of hypoglycemia, particular caution should be taken for symptoms of low blood sugar, and the dosages of other medications may need to be adjusted as necessary. Patients with decreased renal function should undergo regular kidney function tests, and the medication should not be taken if kidney function is severely compromised. Patients with unstable heart function or those with acute heart diseases should use this medication cautiously. In cases where iodinated contrast media is administered during radiological examinations, the use of this medication should be paused before and after the contrast agent administration until renal function stabilizes. For patients undergoing surgery, the medication should be discontinued 48 hours prior to the procedure and can be resumed after confirming normal recovery of kidney function. During the treatment with this medication, acute pancreatitis or skin blistering diseases may occur, so if symptoms such as abdominal pain or skin abnormalities appear, immediate consultation with a doctor is necessary. This medication may lower vitamin B12 levels, so regular checks for vitamin B12 deficiency are needed for long-term use. Pregnant women or those planning to conceive should avoid using this medication, and breastfeeding women are also advised against it. Safety in children and adolescents has not been established, so it should not be used in children under 10 years of age. Elderly patients commonly have decreased renal function; therefore, treatment should be conducted at the minimum dose while regularly monitoring renal function during usage. There is insufficient research on the effects of this medication on driving and operating machinery, so caution is required during use. In case of overdose, treatments such as removing the drug from the gastrointestinal tract or dialysis may be necessary. This medication should be stored in a tightly closed container, avoiding moisture and direct sunlight, and should not be transferred to another container.

Side effects and when to seek care immediately

Serious side effects

Urticaria, angioedema, lactic acidosis, pancreatitis, blistering dermatosis, abnormal liver function (abnormal liver function tests, hepatitis), angina pectoris, acute myocardial infarction, unstable angina, congestive heart failure, cardiac arrest, pneumonia, respiratory distress, asthma, acute kidney injury, end-stage renal disease, cerebral infarction, seizures, severe rash with fever, blistering, skin shedding, oral/ocular mucosal pain, chest tightness, difficulty breathing, cold sweat, paleness.

Mild side effects

  • Nasopharyngitis
  • hypersensitivity
  • hypoglycemia
  • taste disturbances
  • cough
  • decreased appetite
  • diarrhea
  • constipation
  • nausea
  • vomiting
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  • abdominal pain
  • pruritus
  • erythema
  • rash
  • oral ulceration
  • abnormal liver function tests
  • hepatitis
  • severe and disabling arthralgia
  • rhabdomyolysis
  • increased lipase
  • increased amylase
  • elevated triglycerides in the blood
  • decreased hemoglobin
  • increased potassium in the blood
  • increased creatinine in the blood
  • increased creatine phosphokinase level
  • ALT

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. Recommended storage temperature is between 1 and 30 degrees Celsius, to maintain the effectiveness of the drug for a longer period.

Appearance and packaging

Appearance

Bright orange, bilaterally convex oval film-coated tablet

Package unit

10 tablets/bottle, 30 tablets/bottle, 60 tablets/bottle, 100 tablets/bottle, 200 tablets/bottle, 30 tablets/box (10 tablets/PTP x 3)

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.