Medication info
Janshiga S Tablets 10/100 mg (Dapagliflozin, Sitagliptin)

Janshiga S Tablets 10/100 mg (Dapagliflozin, Sitagliptin)

Prescription medicationTablet
Ingredient · strength
Dapagliflozin Propanediol Hydrate›12.3mg / 1 tabletSitagliptin Phosphate Hydrate›128.5mg / 1 tablet
Manufacturer / importer
알보젠코리아(주)
Appearance
Yellow to orange, double-sided, convex round film-coated tablets
Packaging
Box) 28 tablets/box (7 tablets/(Alu-Alu) x 4)
Approval status
Active

MFDS item code 202300072 · Approved 2023.01.06 · Insurance code 652607180

Summary

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

Ingredients

Manufacturer
알보젠코리아(주)

Efficacy & effects

Improvement of blood sugar control in type 2 diabetes

View approved original text

This medication is used to effectively improve blood sugar control in patients with type 2 diabetes who take sitagliptin and dapagliflozin together, in conjunction with diet and exercise therapy.

Dosage and Administration

Adult dosage

This medication can be administered to patients taking sitagliptin 100 mg and dapagliflozin 10 mg, at a dosage of 1 tablet once daily, regardless of meals. The tablet should be swallowed whole.

Precautions

This medication may cause severe allergic reactions due to the sitagliptin component; if symptoms such as skin rash or difficulty breathing occur within 3 months of administration, discontinue use immediately and consult a physician. There is a risk of acute pancreatitis; inform medical staff immediately if there are severe abdominal pain or vomiting. This medication should not be used in patients with type 1 diabetes, diabetic ketoacidosis, or those on dialysis. Patients with impaired kidney function or depleted fluid volume may experience a decrease in blood pressure or worsening kidney function when using this medication; therefore, kidney function and fluid status should be monitored periodically before and during administration. As this medication lowers blood sugar, the risk of hypoglycemia may increase when used with insulin or sulfonylureas, and dosage adjustments may be necessary. This medication may increase the risk of genital infections and urinary tract infections; if infection symptoms occur, immediate treatment is required, and patients with a history of infections should be particularly cautious. Elderly patients or those with impaired liver function may be more affected by this medication, so careful monitoring during use is necessary. Pregnant or breastfeeding women should avoid using this medication and discontinue it immediately if pregnancy is confirmed. This medication does not significantly affect driving or operating machinery, but caution is required as hypoglycemic symptoms may occur. There is no specific antidote for overdose; appropriate treatment based on symptoms should be provided, and dialysis may be considered in severe cases. The safety and efficacy of this medication in children have not been established, so it is recommended not to use it. During treatment, be vigilant for adverse symptoms like fluid volume depletion, hypotension, ketoacidosis, and deterioration of kidney function, and consult medical staff immediately if such symptoms occur.

Side effects and when to seek care immediately

Serious side effects

Urticaria, severe swelling (edema), anaphylaxis, angioedema, Stevens-Johnson syndrome, severe allergic reactions, severe rash with high fever, blisters, skin peeling, painful mucous membranes in the mouth/eyes, severe skin adverse reactions, shortness of breath or difficulty breathing, asthma attacks, respiratory abnormalities with cough and fever, respiratory issues, yellowing of the skin or eyes (jaundice), extreme lethargy, liver abnormalities (jaundice), sudden and

Mild side effects

  • Headache
  • nasopharyngitis
  • upper respiratory tract infection
  • urinary tract infection
  • genital itching
  • dry mouth
  • constipation
  • back pain
  • dysuria
  • polyuria
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  • nocturia
  • increased serum creatinine
  • dyslipidemia
  • weight loss
  • myalgia
  • limb pain
  • back pain
  • dyspepsia
  • nausea
  • diarrhea
  • vomiting
  • paresthesia
  • palpitations
  • insomnia
  • itching
  • cold sweat
  • weakness
  • hunger
  • vaginal discharge
  • irregular menstruation
  • fever
  • foreign body sensation
  • facial pain
  • facial swelling
  • allergy

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

Storage

This medication is sensitive to air and moisture, so it should be stored in a tightly sealed container. The storage temperature should ideally be between 1 and 30 degrees Celsius.

Appearance and packaging

Appearance

Yellow to orange, double-sided, convex round film-coated tablets

Package unit

Box) 28 tablets/box (7 tablets/(Alu-Alu) x 4)

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.