Medication info
Tenegreen Duo Extended-Release Tablet 10/500mg

Tenegreen Duo Extended-Release Tablet 10/500mg

Prescription medicationTablet경구
Ingredient · strength
Teneligliptin Hydrochloride Hydrate›13mg / 1 tabletMetformin Hydrochloride›500mg / 1 tablet
Manufacturer / importer
진양제약(주)
Appearance
Orange, egg-shaped extended-release film-coated tablet
Packaging
30 tablets per bottle
Approval status
Active

MFDS item code 202201440 · Approved 2022.04.04 · Insurance code 650304310

Summary

Main use
Improvement in blood glucose control for type 2 diabetes
Who takes it
Adults
Adult dose
The medication is typically administered once daily with dinner, and the dosage is adjusted gradually. The 20/1000mg extended-release tablet is taken once daily, one tablet at a time. The 10/750mg or 10/500mg extended-release tablets are taken once daily, two tablets together at a time. The initial dosage is teneligliptin 20mg once daily along with the patient's existing metformin dosage. The maximum recommended daily dosage is teneligliptin 20mg.

Ingredients

Manufacturer
진양제약(주)

Efficacy & effects

Improvement in blood glucose control for type 2 diabetes

View approved original text

This medication helps patients with type 2 diabetes achieve better blood glucose control when taken along with diet and exercise. The combination of teneligliptin and metformin works together to stabilize blood sugar levels and assists in overall diabetes management. Consistent use and lifestyle improvements can lead to healthy blood glucose control.

How to take

Adult dose

The medication is typically administered once daily with dinner, and the dosage is adjusted gradually. The 20/1000mg extended-release tablet is taken once daily, one tablet at a time. The 10/750mg or 10/500mg extended-release tablets are taken once daily, two tablets together at a time. The initial dosage is teneligliptin 20mg once daily along with the patient's existing metformin dosage. The maximum recommended daily dosage is teneligliptin 20mg.

Precautions

This medication is used to assist in controlling blood sugar levels for diabetic patients. However, it should not be administered to patients with moderately reduced kidney function or those with severe heart disease or poor liver function. Additionally, patients scheduled for tests using radiocontrast iodine should discontinue this medication 48 hours prior to the test and only resume after confirming normal kidney function post-testing. Women who are pregnant or may become pregnant should avoid taking this medication. Caution should be exercised as taking this medication with other diabetes treatments can result in hypoglycemia, and patients should be well-informed about the symptoms and management of hypoglycemia. Rarely, lactic acidosis may occur during treatment, which can start with symptoms such as muscle pain, weakness, difficulty breathing, and abdominal pain, and can be life-threatening in severe cases, so immediate consultation with healthcare personnel is advised if suspected symptoms arise. Regular monitoring of liver and kidney function is important during treatment, particularly for elderly patients who may have reduced kidney function. Moreover, alcohol consumption can increase the risk of lactic acidosis, hence it is advisable to avoid drinking during treatment. Vitamin B12 levels may decrease during the course of the treatment, thus regular blood tests are recommended. If undergoing surgery or experiencing severe infection, trauma or other conditions affecting overall health, this medication should be temporarily discontinued until recovery. This medication should be stored out of reach of children, and any unusual symptoms or suspected side effects during treatment must be discussed immediately with a physician.

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, skin peeling, pain in oral or ocular mucosa, shortness of breath or difficulty breathing, asthma attack, respiratory abnormalities accompanied by cough and fever, yellowing of the skin or eyes (jaundice), profound lethargy, sudden and extremely severe headache, thunderclap headache, seizures, altered consciousness, visual disturbances, paralysis, urinary changes

Mild side effects

  • Hypoglycemia
  • constipation
  • dizziness
  • headache
  • abdominal pain
  • stomatitis
  • cold sweat
  • itching
  • rash
  • malaise
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  • fatigue
  • diarrhea
  • indigestion
  • increased blood sugar
  • increased blood pressure
  • allergic rhinitis
  • arthralgia
  • abnormal sputum
  • increased serum creatinine
  • increased blood urea
  • elevated serum potassium levels
  • hives
  • shingles
  • nasopharyngitis
  • gastritis
  • gastroesophageal reflux disease
  • vomiting
  • chronic gastritis
  • upper abdominal pain
  • hunger
  • dehydration
  • weakness

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

Storage

This medication should be stored in a tightly sealed container to protect from air, and it is recommended to keep it at room temperature, between 1 to 30 degrees Celsius. Storing it this way helps maintain its effectiveness and safety.

Appearance and packaging

Appearance

Orange, egg-shaped extended-release film-coated tablet

Package unit

30 tablets per 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.