Medication info
Teneligliptin M Extended-Release Tablets 10/750 mg

Teneligliptin M Extended-Release Tablets 10/750 mg

Prescription medicationTablet경구
Ingredient · strength
Metformin Hydrochloride›750mg / 1 tabletTeneligliptin Ditosylate Dihydrate›18.92mg / 1 tablet
Manufacturer / importer
케이엠에스제약(주)
Appearance
Yellow oval-shaped extended-release film-coated tablet
Packaging
30 tablets/bottle
Approval status
Active

MFDS item code 202202734 · Approved 2022.07.01 · Insurance code 654702300

Summary

Main use
Improvement of blood sugar control in type 2 diabetes
Who takes it
Adults
Adult dose
Generally, this medication is taken once daily with the evening meal. The 20/1000mg extended-release tablet is taken once daily, 1 tablet at a time. Patients taking the 10/750mg or 10/500mg extended-release tablets should take 2 tablets simultaneously once a day. The initial dosage is 20mg of teneligliptin once daily along with the established dosage of metformin. The maximum recommended dosage per day is teneligliptin

Ingredients

Manufacturer
케이엠에스제약(주)

Efficacy & effects

Improvement of blood sugar control in type 2 diabetes

View approved original text

This medication is used to assist with blood sugar control in patients with type 2 diabetes by supplementing diet and exercise therapy, specifically helping to effectively manage blood glucose levels and support diabetes treatment.

How to take

Adult dose

Generally, this medication is taken once daily with the evening meal. The 20/1000mg extended-release tablet is taken once daily, 1 tablet at a time. Patients taking the 10/750mg or 10/500mg extended-release tablets should take 2 tablets simultaneously once a day. The initial dosage is 20mg of teneligliptin once daily along with the established dosage of metformin. The maximum recommended dosage per day is teneligliptin

Precautions

This medication is used for the treatment of diabetes and has a blood sugar-lowering effect. This medication should not be administered to patients with impaired kidney function, particularly in cases of moderate to severe renal impairment. In special circumstances such as weakened heart function, acute heart issues, severe infection, or perioperative conditions, the administration of this medication should be temporarily suspended. This medication can cause a rare but serious side effect known as lactic acidosis; thus, if symptoms such as shortness of breath, muscle pain, weakness, or abdominal pain occur, it is crucial to notify a doctor immediately. The risk of hypoglycemia may increase when this medication is used with other diabetes medications, so it is essential to be knowledgeable about hypoglycemia symptoms and how to manage them. Patients with liver impairment or those who drink excessively should avoid using this medication, and liver and kidney functions should be monitored regularly. It is advisable for pregnant women or those who may become pregnant to refrain from taking this medication. While on this medication, it is important to regularly check not only blood sugar levels but also liver function, kidney function, and vitamin B12 levels. Patients engaged in hazardous activities such as driving or working at heights should be particularly vigilant for signs of hypoglycemia or lactic acidosis. This medication may interact with other drugs, so it is imperative to inform healthcare providers of any concurrent medications. Use in children or the elderly may be restricted, and older adults should frequently monitor kidney function and adjust dosages accordingly. In cases of overdose, immediate medical attention should be sought, as blood dialysis may be required. This medication should be kept out of reach of children and transferred to a different container should be avoided.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe allergic reaction, fever accompanied by severe rash, blisters, skin peeling, pain in oral/ocular mucosa, severe skin adverse reactions, shortness of breath or difficulty breathing, asthma attacks, respiratory abnormalities accompanied by cough and fever, respiratory issues, yellowing of the skin or eyes (jaundice), profound lethargy, liver abnormalities (jaundice), sudden and

Mild side effects

  • Hypoglycemia
  • constipation
  • dizziness
  • abdominal bloating
  • abdominal discomfort
  • nausea
  • abdominal pain
  • flatulence
  • stomatitis
  • gastric polyps
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  • colon polyps
  • duodenal ulcers
  • gastroesophageal reflux disease
  • diarrhea
  • decreased appetite
  • increased amylase
  • increased lipase
  • increased AST (GOT)
  • increased ALT (GPT)
  • increased GGT
  • increased ALP
  • proteinuria
  • ketonuria
  • potential hematuria
  • eczema
  • rash
  • itching
  • allergic dermatitis
  • arthralgia
  • increased CK (CPK)

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, and it is recommended to keep it at room temperature ranging from 1 to 30 degrees Celsius. Storing it this way will help maintain the medication's efficacy and safety.

Appearance and packaging

Appearance

Yellow oval-shaped 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.