Medication info
Tecligam Extended-Release Tablet 20/1000 mg

Tecligam Extended-Release Tablet 20/1000 mg

Prescription medicationTablet경구
Ingredient · strength
Teneligliptin Hydrochloride Hydrate›26mg / 1 tabletMetformin Hydrochloride›1000mg / 1 tablet
Manufacturer / importer
신일제약(주)
Appearance
Pink oval extended-release film-coated tablet
Packaging
30 tablets/bottle
Approval status
Active

MFDS item code 202201312 · Approved 2022.04.04 · Insurance code 653806030

Summary

Main use
Improvement of blood sugar control in type 2 diabetes
Who takes it
Adults
Adult dose
This medication is typically administered once daily with the evening meal, with the 20/1000 mg extended-release tablet taken as 1 tablet daily. Patients taking the 10/750 mg or 10/500 mg extended-release tablets should take 2 tablets simultaneously once a day. The initial dose of teneligliptin is 20 mg once daily, alongside the existing dose of metformin. The maximum recommended daily dose is 20 mg of teneligliptin.

Ingredients

Manufacturer
신일제약(주)

Efficacy & effects

Improvement of blood sugar control in type 2 diabetes

View approved original text

This medication helps control blood sugar levels in patients with type 2 diabetes by using teneligliptin and metformin together. It can improve blood sugar control as an adjunct when diet and exercise alone are insufficient for adequate blood sugar management. This aids in the stable management of blood sugar levels and contributes to diabetes treatment.

How to take

Adult dose

This medication is typically administered once daily with the evening meal, with the 20/1000 mg extended-release tablet taken as 1 tablet daily. Patients taking the 10/750 mg or 10/500 mg extended-release tablets should take 2 tablets simultaneously once a day. The initial dose of teneligliptin is 20 mg once daily, alongside the existing dose of metformin. The maximum recommended daily dose is 20 mg of teneligliptin.

Precautions

This medication is used to control blood sugar and caution is required due to the risk of a rare side effect called lactic acidosis. Lactic acidosis is a serious condition caused by excessive accumulation of lactate in the blood, with symptoms such as fatigue, muscle pain, shortness of breath, and abdominal pain. This medication should not be used in patients with severely impaired kidney function, heart failure, liver dysfunction, acute infections, trauma, or those scheduled for surgery. Additionally, it is safest not to administer this medication to women who are pregnant or may become pregnant. When using this medication with other diabetes treatments, the risk of hypoglycemia may increase, so it is essential to be well-informed about the symptoms of hypoglycemia and how to respond. During treatment, regular monitoring of kidney function and blood levels of vitamin B12 should be conducted to check for abnormalities. Alcohol consumption may increase the risk of lactic acidosis; therefore, it is advisable not to drink excessively during treatment. If undergoing surgery or contrast examinations, medication should be paused for a specific period, and treatment can resume once normal kidney function is confirmed. Some patients may experience side effects such as constipation, abdominal pain, and dizziness; if symptoms are severe, consult a physician. Elderly patients may commonly experience decreased kidney function, necessitating dose adjustments and regular testing. During the course of treatment, if sudden severe abdominal pain, vomiting, or the formation of blisters on the skin occurs, medical personnel should be notified immediately.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, peeling skin, pain in mucous membranes of the mouth/eyes, shortness of breath or difficulty breathing, asthma attacks, respiratory abnormalities accompanied by cough and fever, yellowing of the skin or eyes (jaundice), extreme fatigue, sudden and severe headaches, thunderclap headaches, seizures, confusion, visual disturbances, paralysis, urination issues

Mild side effects

  • Dizziness
  • constipation
  • abdominal discomfort
  • nausea
  • abdominal pain
  • bloating
  • stomatitis
  • gastric polyps
  • colon polyps
  • duodenal ulcers
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  • gastroesophageal reflux disease
  • diarrhea
  • decreased appetite
  • elevated amylase
  • elevated lipase
  • elevated AST (GOT)
  • elevated ALT (GPT)
  • elevated GGT
  • elevated ALP
  • proteinuria
  • ketonuria
  • potential hematuria
  • eczema
  • rash
  • itching
  • allergic skin reactions
  • arthralgia
  • elevated CK (CPK)
  • serum potassium elevation

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 air or moisture entry, and it is recommended to keep it at room temperature between 1 and 30 degrees Celsius. This way, the medication's efficacy can be maintained, and it can be used safely.

Appearance and packaging

Appearance

Pink oval extended-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.