Medication info

Glitinaduo Tablet 2.5/1000 mg

Prescription medicationTablet경구Expired
Ingredient · strength
Linagliptin›2.5mg / 1 tabletMetformin Hydrochloride›1000mg / 1 tablet
Manufacturer / importer
삼익제약(주)
Appearance
Light pink, oblong, biconvex film-coated tablet
Packaging
PTP - 60 tablets/PTP [10 tablets/PTP X 6]
Approval status
Expired

MFDS item code 201906454 · Approved 2019.09.16

This product's status changed to Expired on 2024.09.16. 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 treated with metformin: Take this medication 2.5/500 mg twice daily, 1 tablet each time, and may increase up to 2.5/1000 mg, 1 tablet twice daily. 2. If sufficient blood sugar control cannot be achieved with metformin monotherapy: Administer linagliptin 2.5 mg twice daily and existing metformin dosage.

Ingredients

Manufacturer
삼익제약(주)

Efficacy & effects

Improvement of blood sugar control in adults with type 2 diabetes

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

This medication is used to assist blood sugar control in adults with type 2 diabetes. It is administered to patients who have not been previously treated for diabetes or have difficulty controlling blood sugar with monotherapy. It is also used when sufficient blood sugar control has not been achieved with metformin monotherapy or a combination of linagliptin and metformin. In cases where blood sugar control is difficult with the maximum dose of metformin in combination with sulfonylureas, insulin, or empagliflozin, this medication can be added to enhance therapeutic effect. Thus, this medication is used at various treatment stages to complement existing therapies and improve blood sugar control.

How to take

Adult dose

This medication is administered twice daily with meals. 1. If currently not treated with metformin: Take this medication 2.5/500 mg twice daily, 1 tablet each time, and may increase up to 2.5/1000 mg, 1 tablet twice daily. 2. If sufficient blood sugar control cannot be achieved with metformin monotherapy: Administer linagliptin 2.5 mg twice daily and existing metformin dosage.

Precautions

This medication may cause a rare but serious side effect known as lactic acidosis, so it should not be used by patients with impaired kidney function or liver dysfunction. It should not be administered to patients who are allergic to the active ingredients or have certain heart and kidney conditions such as type 1 diabetes, diabetic ketoacidosis, or acute myocardial infarction. Due to the risk of hypoglycemia, blood sugar levels should be closely monitored and dosages adjusted when used in conjunction with other hypoglycemic agents such as insulin or sulfonylureas. Elderly patients with decreased kidney function or those taking medications that affect kidney function should undergo regular kidney function tests, and this medication should be temporarily discontinued in situations where kidney function may rapidly decline. Skin conditions such as acute pancreatitis or bullous pemphigoid may occur, so if persistent, severe abdominal pain or skin rash develops during treatment, consult a physician immediately. It is advisable to avoid using this medication in pregnant women or nursing mothers, and if planning a pregnancy, alternative treatment options should be discussed with a physician. Safety and efficacy in children and adolescents have not been established, thus usage is not recommended for children under 10 years of age. Alcohol consumption should be avoided during treatment, as the risk of lactic acidosis may increase, especially in cases of acute alcohol intoxication. If administration of radiologic iodinated contrast agents is required, this medication should be discontinued for a certain period before and after the examination, and kidney function should be reassessed. In cases of overdose, the risk of lactic acidosis is increased, thus immediate hospital treatment is necessary, which may include blood dialysis. Store this medication in a place out of reach of children, avoid moisture, and do not transfer to another container.

Side effects and when to seek care immediately

Serious side effects

  • Urticaria
  • angioedema
  • lactic acidosis
  • pancreatitis
  • bullous pemphigoid
  • liver abnormalities (including jaundice)
  • severe allergic reactions
  • severe neurological symptoms
  • severe edema
  • acute myocardial infarction
Show 6 more
  • shock
  • sepsis
  • acute renal failure
  • congestive heart failure
  • acute pancreatitis
  • severe joint pain with disability

Mild side effects

Nasopharyngitis, taste disturbance, cough, decreased appetite, diarrhea, constipation, nausea, vomiting, abdominal pain, pruritus, rash, decreased blood B12, mouth ulcer formation, abnormal liver function tests, hepatitis, erythema, joint pain without severe or disabling symptoms, increased lipase, increased amylase, increased triglycerides in the blood, dizziness, insomnia, depression, anxiety, itching, decreased hemoglobin, increased blood pressure, musculoskeletal pain, fatigue, runny nose

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

Storage

This medication is sensitive to air and moisture, thus it should be stored in a sealed container. It is important to maintain storage temperature between 1 degree and 30 degrees Celsius. This helps ensure the medication's effectiveness and maintain quality.

Appearance and packaging

Appearance

Light pink, oblong, biconvex film-coated tablet

Package unit

PTP - 60 tablets/PTP [10 tablets/PTP X 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.

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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.