Medication info
DuoGly Tablet

DuoGly Tablet

Prescription medicationTablet
Ingredient · strength
Sitagliptin Hydrochloride Hydrate›113.4mg / 1 tabletDapagliflozin citric acid›14.7mg / 1 tablet
Manufacturer / importer
대한뉴팜(주)
Appearance
Yellow rectangular film-coated tablet
Packaging
28 tablets/box [7 tablets/PTP × 4], 30 tablets/box [10 tablets/PTP × 3]
Approval status
Active

MFDS item code 202200497 · Approved 2022.01.28 · Insurance code 669908260

Summary

Main use
Improvement of blood sugar control in type 2 diabetes
Who uses it
Adults
Adult dosage
This medication can be taken by patients receiving 100 mg of sitagliptin and 10 mg of dapagliflozin, at a dose of 1 tablet once daily, regardless of meals. The tablet should be swallowed whole.

Ingredients

Manufacturer
대한뉴팜(주)

Efficacy & effects

Improvement of blood sugar control in type 2 diabetes

View approved original text

This medication is used to complement diet and exercise regimens to improve blood sugar control in patients with type 2 diabetes. It is particularly effective for patients suitable for combination therapy with sitagliptin and dapagliflozin. It helps maintain a healthy lifestyle by managing blood sugar levels more stably.

Dosage and Administration

Adult dosage

This medication can be taken by patients receiving 100 mg of sitagliptin and 10 mg of dapagliflozin, at a dose of 1 tablet once daily, regardless of meals. The tablet should be swallowed whole.

Precautions

This medication may cause hypersensitivity reactions, so if any allergic symptoms or skin conditions occur within the first 3 months, usage should be discontinued immediately. Acute pancreatitis may occur; if abdominal pain or symptoms of pancreatitis such as vomiting appear, consult a doctor immediately. Patients with hypersensitivity to any of the active ingredients or additives, as well as those with type 1 diabetes, diabetic ketoacidosis, certain genetic lactase deficiency disorders, and those undergoing dialysis, should not use this medication. Patients with renal impairment or elderly patients at risk of decreased fluid volume, as well as those on diuretics, should assess renal function and fluid status before taking this medication and should monitor periodically during treatment. Side effects such as genital infections, urinary tract infections, hypoglycemia, decreased fluid volume, headache, dry mouth, and constipation may occur while taking this medication, so if any symptoms arise, inform healthcare professionals and receive appropriate treatment. Especially since this medication has a blood sugar-lowering effect, the risk of hypoglycemia increases when taken with other hypoglycemic agents such as insulin or sulfonylureas, thus dosage adjustment may be necessary. Women who are pregnant or breastfeeding should avoid using this medication and discontinue its use immediately upon confirmation of pregnancy. For children under 18 years of age, the safety and efficacy of this medication have not been established, so it should not be used. In case of overdose, there is no specific antidote; visit a healthcare facility immediately for treatment according to symptoms, and dialysis may be considered if needed. This medication does not significantly affect driving or machinery operation, but caution is advised due to the possibility of hypoglycemic symptoms.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweats, pallor, anaphylaxis, angioedema, Stevens-Johnson syndrome, acute pancreatitis, hemorrhagic or necrotizing pancreatitis, severe skin adverse reactions, severe and disabling arthralgia, blistering similar to pemphigus, worsening renal function, acute renal failure, neurological abnormalities (severe headache, lightning headache, seizures, confusion, vision changes, paralysis), perineum

Mild side effects

  • Headache
  • upper respiratory tract infection
  • nasopharyngitis
  • constipation
  • nausea
  • diarrhea
  • dry mouth
  • back pain
  • dysuria
  • genital itching
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  • hair loss
  • dermatitis
  • itching
  • cold sweats
  • fatigue
  • pain
  • hunger
  • palpitations
  • insomnia
  • decreased appetite
  • drowsiness
  • indigestion
  • nausea
  • vomiting
  • urinary retention
  • taste disturbance
  • drowsiness
  • tension headache
  • fainting
  • tremor
  • arthralgia
  • musculoskeletal pain
  • limb pain
  • myalgia
  • osteoarthritis
  • ligament sprains
  • dry eye
  • eye pain
  • vision changes

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

Storage

This medication is sensitive to air and moisture, so it must be stored in a tightly sealed container. It is important to maintain storage temperature between 1 and 30 degrees Celsius. Avoid storing in excessively hot or cold places.

Appearance and packaging

Appearance

Yellow rectangular film-coated tablet

Package unit

28 tablets/box [7 tablets/PTP × 4], 30 tablets/box [10 tablets/PTP × 3]

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

No questions yet.

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.