Medication info
Tenelia M Sustained Release Tablet 20/1000 mg

Tenelia M Sustained Release Tablet 20/1000 mg

Prescription medicationTablet경구
Ingredient · strength
Metformin Hydrochloride›1000mg / 1 tabletTeneligliptin Hydrobromide Hydrate›31mg / 1 tablet
Manufacturer / importer
(주)한독
Appearance
Pink egg-shaped sustained release film-coated tablet
Packaging
30 tablets/bottle
Approval status
Active

MFDS item code 201501700 · Approved 2015.03.31 · Insurance code 652105480

Summary

Main use
Improvement in blood sugar control in type 2 diabetes
Who takes it
Adults
Adult dose
This medication is generally taken once daily with the evening meal, specifically 1 tablet of the 20/1000 mg sustained release tablet. For the 10/750 mg or 10/500 mg sustained release tablets, 2 tablets are taken simultaneously once daily. The initial dose should consist of 20 mg of Teneligliptin once daily along with the patient's existing dosage of Metformin. The maximum recommended daily dose is 20 mg of Teneligliptin and 2000 mg of sustained release Metformin.

Ingredients

Manufacturer
(주)한독

Efficacy & effects

Improvement in blood sugar control in type 2 diabetes

View approved original text

This medication is used in conjunction with diet control and exercise therapy to help patients with type 2 diabetes who need to take Teneligliptin and Metformin together manage their blood sugar levels.

How to take

Adult dose

This medication is generally taken once daily with the evening meal, specifically 1 tablet of the 20/1000 mg sustained release tablet. For the 10/750 mg or 10/500 mg sustained release tablets, 2 tablets are taken simultaneously once daily. The initial dose should consist of 20 mg of Teneligliptin once daily along with the patient's existing dosage of Metformin. The maximum recommended daily dose is 20 mg of Teneligliptin and 2000 mg of sustained release Metformin.

Precautions

This medication helps to control blood sugar levels, and there are several precautions to consider when using it. First, it can rarely cause a serious condition known as lactic acidosis, so patients with impaired kidney function, heart disease, or compromised liver function should avoid using this medication. Additionally, symptoms of hypoglycemia may occur when used with insulin or other diabetes medications, so it is important to know the symptoms of hypoglycemia and take appropriate measures immediately if they occur. This medication should not be administered to patients with reduced kidney function, and those scheduled for surgery or radiologic contrast examinations should stop taking it at least 48 hours prior and resume only after confirming normal kidney function. Women who are pregnant or may become pregnant, patients with severe infections, trauma, or malnutrition should also avoid using this medication. Regular monitoring of liver and kidney function is necessary while taking this medication, and it is advisable to avoid alcohol consumption. This medication may lower vitamin B12 levels, so it is important to check vitamin B12 levels with long-term use. Moreover, if severe sudden abdominal pain, vomiting, or difficulty breathing occurs during the course of this medication, consult a physician immediately. Elderly patients or those with reduced kidney function require dosage adjustments and regular function tests, and care should be taken when performing tasks requiring concentration, such as driving or working at heights, considering the risk of hypoglycemia and lactic acidosis. Finally, safety and efficacy in children have not been established, so this medication is not used for children.

Side effects and when to seek care immediately

Serious side effects

Lactic acidosis (severe lactic acidosis), liver dysfunction (interstitial pneumonia, liver dysfunction, toxic hepatitis), bullous pemphigoid (pemphigoid), acute pancreatitis, severe neurological symptoms (cerebral infarction, hepatic coma, peripheral neuropathy, facial paralysis, sciatica, orthostatic dizziness), severe allergic reactions (severe urticaria, severe edema), respiratory issues (difficulty breathing, asthma attacks, stridor)

Mild side effects

  • Hypoglycemia
  • constipation
  • dizziness
  • headache
  • nausea
  • abdominal pain
  • diarrhea
  • decreased appetite
  • itching
  • allergic dermatitis
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  • joint pain
  • malaise
  • allergic rhinitis
  • elevated serum uric acid
  • peripheral edema
  • upper abdominal pain
  • gastritis
  • viral upper respiratory infection
  • fatigue
  • trembling
  • weakness
  • hunger
  • facial edema
  • dyspepsia
  • nausea
  • sweating
  • diabetic retinopathy
  • vision decline
  • cough
  • pulmonary congestion
  • difficulty breathing
  • drug overdose
  • benign prostatic hyperplasia

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

Storage

Store this medication in a sealed container to prevent air or moisture from entering, and it is best to keep it at room temperature between 1 to 30 degrees Celsius. Storing it this way helps maintain the effectiveness of the medication and ensures safe use.

Appearance and packaging

Appearance

Pink egg-shaped 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.