Medication info
Jadis Duo Tablets 5/500 mg (Empagliflozin, Metformin)

Jadis Duo Tablets 5/500 mg (Empagliflozin, Metformin)

Prescription medicationTablet경구
Ingredient · strength
Empagliflozin›5mg / 1 tabletMetformin Hydrochloride›500mg / 1 tablet
Manufacturer / importer
하나제약(주)
Appearance
Orange-yellow, biconvex, oval film-coated tablet
Packaging
10 tablets/box [10 tablets/PTP x 1], 30 tablets/bottle, 60 tablets/box [10 tablets/PTP x 6], 60 tablets/bottle
Approval status
Active

MFDS item code 202201353 · Approved 2022.04.04 · Insurance code 657808280

Summary

Main use
Effectiveness in controlling blood sugar in type 2 diabetes and preventing cardiovascular events
Who takes it
Adults
Adult dose
The recommended dose of this drug is 1 tablet, twice a day. For patients who do not achieve adequate blood glucose control with metformin alone or in combination with other medications such as insulin, empagliflozin 5 mg should be taken twice daily (total of 10 mg), and if tolerability is good, the dosage can be increased to 10 mg to 25 mg. Patients using a combination therapy of empagliflozin and metformin should administer their existing dosage. This drug is for use with meals.

Ingredients

Manufacturer
하나제약(주)

Efficacy & effects

Effectiveness in controlling blood sugar in type 2 diabetes and preventing cardiovascular events

View approved original text

This drug is used to effectively improve blood sugar levels in adults with type 2 diabetes who cannot achieve proper control with diet and exercise alone, through the combined action of empagliflozin and metformin. It is particularly suitable for patients whose blood sugar is not sufficiently controlled, and can also be administered to patients with type 2 diabetes who have cardiovascular disease. However, risks associated with cardiovascular events should be referred to professional guidelines. This drug contributes to safely controlling blood sugar and assisting in diabetes management.

How to take

Adult dose

The recommended dose of this drug is 1 tablet, twice a day. For patients who do not achieve adequate blood glucose control with metformin alone or in combination with other medications such as insulin, empagliflozin 5 mg should be taken twice daily (total of 10 mg), and if tolerability is good, the dosage can be increased to 10 mg to 25 mg. Patients using a combination therapy of empagliflozin and metformin should administer their existing dosage. This drug is for use with meals.

Precautions

This drug can cause severe lactic acidosis, so it should not be used in patients with poor kidney function, severe infection, or dehydration. Additionally, caution should be taken as there is a risk of hypoglycemia when taken with insulin or sulfonylureas. This drug is not administered to patients with moderate to severe kidney dysfunction or in situations where acute kidney injury is anticipated. Patients with acute heart disease, heart failure, liver dysfunction, pregnant or breastfeeding women should also avoid this drug. Regular kidney function tests should be conducted before and during use of this drug, especially in elderly patients or those with diminished kidney function. This drug can influence body fluid volume and carries a risk of dehydration or low blood pressure, so caution should be exercised in patients with dehydration symptoms or low blood pressure. During treatment, patients must be alert to symptoms of hypoglycemia resulting from excessively low blood sugar, and should be cautious about irregular meals or excessive exercise as these may increase risks. Genital and urinary infections may occur, so if related symptoms arise, consultation with a doctor should be sought immediately. Women who are pregnant or planning to become pregnant should not use this drug, and breastfeeding women are also advised to avoid it. If surgery is planned or diagnostic tests using iodinated contrast agents are to be conducted, this drug should be temporarily discontinued, and it should only be resumed after confirming that kidney function is normal. In cases of overdose, serious side effects such as lactic acidosis may occur, so immediate medical attention is required. This drug has not been established as safe and effective in children, so it should not be used in individuals under 18 years of age. Elderly patients carry a higher risk of kidney dysfunction and fluid loss, thus requiring dosage adjustments and monitoring of kidney function. Alcohol consumption may increase the risk of lactic acidosis, so it is advisable to avoid it while taking this medication. During the use of this drug, it is important to consult with a healthcare professional if abnormal symptoms occur, and to regularly check for any side effects.

Side effects and when to seek care immediately

Serious side effects

  • Severe lactic acidosis
  • lactic acidosis
  • ketoacidosis
  • urticaria
  • angioedema
  • severe rash with high fever
  • blisters
  • skin peeling
  • oral/eye mucosal pain
  • perineal necrosis
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  • urosepsis
  • pyelonephritis
  • pneumonia
  • sepsis
  • severe allergic reaction
  • liver abnormalities (jaundice)
  • sudden and very severe headache
  • stroke
  • concussion
  • cerebral infarction
  • intracranial aneurysm
  • seizures
  • confusion
  • visual disturbances
  • paralysis
  • severe swelling
  • or urinary issues

Mild side effects

  • Hypoglycemia
  • urinary tract infection
  • genital infection
  • increased urination
  • nausea
  • vomiting
  • diarrhea
  • abdominal pain
  • loss of appetite
  • constipation
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  • abnormal liver function tests
  • hepatitis
  • taste disturbance
  • itching
  • rash
  • erythema
  • urticaria
  • angioedema
  • increased serum creatinine
  • increased serum lipids
  • decreased fluid volume
  • thirst
  • abnormal diagnostic tests
  • decreased and deficiency of vitamin B12
  • headache
  • dizziness
  • drowsiness
  • weakness
  • insomnia
  • anxiety
  • fatigue
  • chest discomfort
  • chest pain

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

Storage

This drug should be stored in a tightly closed container to avoid exposure to air or moisture, ideally at room temperature between 1 and 30 degrees Celsius. Taking these precautions will help maintain the drug's effectiveness.

Appearance and packaging

Appearance

Orange-yellow, biconvex, oval film-coated tablet

Package unit

10 tablets/box [10 tablets/PTP x 1], 30 tablets/bottle, 60 tablets/box [10 tablets/PTP x 6], 60 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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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.