Medication info
Polminlina Sustained Release Tablet 2.5/1000 mg (Linagliptin, Metformin Hydrochloride)

Polminlina Sustained Release Tablet 2.5/1000 mg (Linagliptin, Metformin Hydrochloride)

Prescription medicationTablet경구
Ingredient · strength
Linagliptin Micronized›2.5mg / 1 tabletMetformin Hydrochloride›1000mg / 1 tablet
Manufacturer / importer
(주)녹십자
Appearance
White oval sustained release film-coated tablet
Packaging
30 tablets/bottle
Approval status
Active

MFDS item code 202400695 · Approved 2024.03.29 · Insurance code 643606680

Summary

Main use
Improvement of blood sugar control in type 2 diabetes
Who takes it
Adults
Adult dose
This medication is taken once daily with the evening meal. 5/1000 mg sustained release tablet is taken once a day, at a dose of 1 tablet at a time. 2.5/1000 mg sustained release tablet is taken once a day, at a dose of 2 tablets simultaneously. The initial dosage is Linagliptin 5 mg and Metformin Hydrochloride 1000 mg, and Metformin Hydrochloride can be gradually increased to a maximum recommended daily dose of 2000 mg. Currently, Metformin.

Ingredients

Manufacturer
(주)녹십자

Efficacy & effects

Improvement of blood sugar control in type 2 diabetes

View approved original text

This medication is used to assist patients with type 2 diabetes who need to take Linagliptin and Metformin together in controlling their blood sugar levels. It helps manage blood sugar effectively in conjunction with diet and exercise therapy. This assists in improving the health of patients who struggle with blood sugar control.

How to take

Adult dose

This medication is taken once daily with the evening meal. 5/1000 mg sustained release tablet is taken once a day, at a dose of 1 tablet at a time. 2.5/1000 mg sustained release tablet is taken once a day, at a dose of 2 tablets simultaneously. The initial dosage is Linagliptin 5 mg and Metformin Hydrochloride 1000 mg, and Metformin Hydrochloride can be gradually increased to a maximum recommended daily dose of 2000 mg. Currently, Metformin.

Precautions

This medication assists in controlling blood sugar levels. However, it may rarely cause a serious condition known as lactic acidosis, so caution is advised. It should not be used in individuals with allergies to its components or those with type 1 diabetes, severe renal impairment, acute cardiac conditions, liver dysfunction, etc. Also, it should be avoided in the presence of acute diseases such as dehydration, severe infections, or shock. Care must be taken for hypoglycemic symptoms when using this medication, especially when taken with other hypoglycemic agents. Patients with reduced renal function should undergo regular kidney function tests, and medication dosage adjustments may be necessary depending on their condition. Acute pancreatitis or blistering skin diseases may occur; therefore, if severe abdominal pain or skin abnormalities occur during treatment, inform a healthcare provider immediately. This medication should be swallowed whole and must not be broken, crushed, or chewed; the tablet coating may pass in the stool, which is normal. It is advisable to avoid using this medication during pregnancy or breastfeeding. Elderly patients should use this medication with increased caution due to a higher risk of renal impairment, with regular kidney function tests required. Additionally, this medication may pose risks when taken with alcohol, so it is better to avoid drinking. While receiving this medication, blood sugar levels and health status should be closely monitored, and if any abnormal symptoms appear, a healthcare provider should be consulted immediately.

Side effects and when to seek care immediately

Serious side effects

  • Urticaria
  • angioedema
  • lactic acidosis
  • angioedema
  • urticaria
  • angioedema
  • angioedema
  • angioedema
  • angioedema
  • urticaria
Show 17 more
  • angioedema
  • angioedema
  • angioedema
  • angioedema
  • angioedema
  • angioedema
  • angioedema
  • angioedema
  • angioedema
  • angioedema
  • angioedema
  • angioedema
  • angioedema
  • angioedema
  • angioedema
  • angioedema
  • angioedema.

Mild side effects

  • Pharyngitis
  • taste disturbance
  • cough
  • loss of appetite
  • diarrhea
  • constipation
  • nausea
  • vomiting
  • abdominal pain
  • oral ulceration
Show 19 more
  • itching
  • rash
  • increased serum triglycerides
  • increased amylase
  • abnormal vitamin B12 absorption test
  • abnormal liver function tests
  • hepatitis
  • erythema
  • severe and disabling arthralgia
  • rhabdomyolysis
  • angioedema
  • urticaria
  • similar to pemphigus
  • angioedema
  • itching
  • erythema
  • rash
  • severe and disabling arthralgia
  • rhabdomyolysis.

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

Storage

This medication should be stored in a tightly closed container to prevent exposure to air or moisture. It is best to store it at room temperature, between 1 to 30 degrees Celsius.

Appearance and packaging

Appearance

White oval sustained release film-coated tablet

Package unit

30 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.