Medication info
Teddy-PM Extended Release Tablet 10/750 mg

Teddy-PM Extended Release Tablet 10/750 mg

Prescription medicationTablet경구
Ingredient · strength
Teneligliptin Hydrochloride Hydrate›13mg / 1 tabletMetformin Hydrochloride›750mg / 1 tablet
Manufacturer / importer
동광제약(주)
Appearance
Yellow oval extended release film-coated tablet
Packaging
30 tablets/bottle
Approval status
Active

MFDS item code 202201498 · Approved 2022.04.08 · Insurance code 645907310

Summary

Main use
Improvement of blood glucose control in type 2 diabetes
Who takes it
Adults
Adult dose
This medication is generally administered once daily with the evening meal, and the dosage is adjusted gradually to reduce gastrointestinal side effects associated with metformin. The 20/1000 mg extended release tablet is taken once daily, one tablet at a time. Patients on the 10/750 mg or 10/500 mg extended release tablets should take two tablets simultaneously once daily. Adequate blood glucose control should be achieved in patients treated with metformin monotherapy.

Ingredients

Manufacturer
동광제약(주)

Efficacy & effects

Improvement of blood glucose control in type 2 diabetes

View approved original text

This medication is used in conjunction with dietary therapy and exercise therapy to help control blood glucose levels in patients with type 2 diabetes. Teneligliptin and metformin work together to effectively lower blood glucose levels, providing assistance for blood glucose management. This can serve as a useful treatment option for patients who struggle with blood glucose control. Consistent use, along with healthy lifestyle habits, can contribute to improved blood glucose levels.

How to take

Adult dose

This medication is generally administered once daily with the evening meal, and the dosage is adjusted gradually to reduce gastrointestinal side effects associated with metformin. The 20/1000 mg extended release tablet is taken once daily, one tablet at a time. Patients on the 10/750 mg or 10/500 mg extended release tablets should take two tablets simultaneously once daily. Adequate blood glucose control should be achieved in patients treated with metformin monotherapy.

Precautions

This medication is used to treat diabetes and assist with blood glucose control. However, it should not be used in patients with poor kidney function or severe heart disease or liver dysfunction. In particular, in cases of decreased kidney function, the medication can accumulate in the body and cause lactic acidosis, which is a potentially dangerous condition, so caution is needed. Additionally, when used along with other diabetes medications, hypoglycemia may occur, so blood glucose levels should be closely monitored. Before and after surgery or radiographic tests involving contrast agents, medication use should be temporarily stopped and restarted only after confirming normal kidney function. Women who are pregnant or may become pregnant, as well as breastfeeding women, should avoid using this medication. Alcohol consumption should be avoided while taking this medication, and if symptoms such as dizziness, abdominal pain, or difficulty breathing occur, immediate consultation with medical personnel is necessary. Older adults may have decreased kidney function, so regular kidney function tests and appropriate dosage adjustments are required. Also, this medication may lower vitamin B12 levels, so periodic blood tests are needed for monitoring during long-term use. While taking this medication, sufficient knowledge of hypoglycemic symptoms and measures should be acquired, and caution is needed when driving or performing high-risk work. Furthermore, drug interactions may occur when used in combination with other medications, so any concurrent medications should be disclosed to medical personnel.

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 fever, blisters, skin peeling, pain in mouth/eye mucosa, shortness of breath or difficulty breathing, asthma attacks, respiratory abnormalities accompanied by cough and fever, yellowing of skin or eyes (jaundice), severe lethargy, sudden and severe headaches, thunderclap headaches, seizures, confusion of consciousness, visual disturbances, paralysis, urination

Mild side effects

  • Hypoglycemia
  • constipation
  • dizziness
  • headache
  • weakness
  • hunger
  • fatigue
  • facial swelling
  • diarrhea
  • indigestion
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  • nausea
  • itching
  • cough
  • rash
  • allergic dermatitis
  • joint pain
  • malaise
  • allergic rhinitis
  • elevated serum uric acid
  • peripheral edema
  • upper abdominal pain
  • gastritis
  • viral upper respiratory infection
  • shingles
  • nasopharyngitis
  • cold sweat
  • vision changes
  • pulmonary congestion
  • difficulty breathing
  • prostate enlargement
  • dizziness
  • tremor
  • headache
  • stomatitis

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

Storage

This medication should be stored in a tightly sealed container that is well-ventilated, and kept at a temperature between 1 and 30 degrees Celsius. Proper storage helps to maintain the medication's efficacy and prevent deterioration.

Appearance and packaging

Appearance

Yellow 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.