Medication info

Januritin ES Tablet 100 mg (Sitagliptin Phosphate Hydrate)

Prescription medicationTablet경구Expired
Ingredient · strength
Sitagliptin Phosphate Hydrate›128.5mg / 1 tablet
Manufacturer / importer
대원제약(주)
Appearance
Beige colored, round, biconvex film-coated tablet
Packaging
28 tablets/box [(14 tablets/PTPX2)]
Approval status
Expired

MFDS item code 201502304 · Approved 2015.04.16

This product's status changed to Expired on 2025.04.16. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Improvement of blood sugar control in type 2 diabetes
Who takes it
Adults
Adult dose
This medication is administered once daily at a dose of 100 mg either as monotherapy or in combination therapy, with a maximum daily dose of 100 mg. It may be taken regardless of meals. For patients with renal impairment, dose adjustments are needed based on kidney function. Patients with mild to moderate renal impairment (eGFR 45 to less than 90) do not require dose adjustments. Patients with moderate renal impairment (eGFR 30 to less than 45) should take 50 mg once daily.

Ingredients

Manufacturer
대원제약(주)

Efficacy & effects

Improvement of blood sugar control in type 2 diabetes

  • Difficulty in blood sugar control in patients with type 2 diabetes
View approved original text

This medication is used in conjunction with diet and exercise to improve blood sugar control in patients with type 2 diabetes. It may be initiated as monotherapy but can be used with metformin if blood sugar control is difficult in patients who have not previously received diabetes medication. This drug can also be administered to enhance the effectiveness when adequate control cannot be achieved with monotherapy using sulfonylureas, metformin, thiazolidinediones, or insulin. It is added in combination therapy when difficulties with blood sugar control are present. This versatility helps to improve blood sugar control.

How to take

Adult dose

This medication is administered once daily at a dose of 100 mg either as monotherapy or in combination therapy, with a maximum daily dose of 100 mg. It may be taken regardless of meals. For patients with renal impairment, dose adjustments are needed based on kidney function. Patients with mild to moderate renal impairment (eGFR 45 to less than 90) do not require dose adjustments. Patients with moderate renal impairment (eGFR 30 to less than 45) should take 50 mg once daily.

Precautions

This medication may rarely cause severe allergic reactions after administration. If symptoms such as skin rash or difficulty breathing occur, discontinue use immediately and consult a physician. Acute pancreatitis may occur during treatment with this medication, so notify healthcare personnel immediately if symptoms such as abdominal pain, nausea, or vomiting arise. This medication should not be used in patients with type 1 diabetes or diabetic ketoacidosis, nor in patients who are allergic to this medication or its components. Patients with impaired kidney function may need dose adjustments and should undergo regular kidney function tests. This medication may be used alone or in conjunction with other diabetes treatments, but caution is advised as the risk of hypoglycemia may increase when used with insulin or sulfonylureas. During treatment, symptoms such as headache, upper respiratory infection, nasopharyngitis, dyspepsia, diarrhea, and muscle aches may occur; if these persist or worsen, consult a physician. This medication is not recommended for use in pregnant or breastfeeding women, nor in children and adolescents under 18 years old, as safety and efficacy have not been established. Due to the potential for decreased renal function in older adults, dose adjustments and monitoring of kidney function are necessary. In case of overdose, seek medical attention immediately for appropriate treatment, as some may be removed by dialysis. If skin blisters or soreness occur during treatment, consult a physician immediately for treatment, and consider stopping the medication if severe or persistent joint pain occurs. There is a possibility of drug interactions when taken with other medications, so always inform healthcare personnel about other medications being taken, especially when used with cyclosporine or digoxin, as caution is needed.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (angioedema), anaphylaxis, exfoliative skin conditions (including Stevens-Johnson syndrome), acute pancreatitis, acute kidney failure, severe hypoglycemia, blistering pemphigoid, jaundice (liver dysfunction), cardiac arrest, pneumonia, diabetes complications, metabolic acidosis, severe neurological symptoms (confusion, seizures, etc.)

Mild side effects

  • Nasopharyngitis
  • upper respiratory infection
  • headache
  • diarrhea
  • dyspepsia
  • nausea
  • muscle pain
  • limb pain
  • back pain
  • pruritus
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  • thrombocytopenia
  • dizziness
  • elevated blood triglycerides
  • increased low-density lipoprotein
  • hyperglycemia
  • constipation
  • vomiting
  • severe and debilitating joint pain.

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

Storage

This medication should be stored in a tightly closed container to prevent air and moisture from entering, at room temperature between 1 and 30 degrees Celsius. Proper storage will help maintain the drug's effectiveness and prevent degradation.

Appearance and packaging

Appearance

Beige colored, round, biconvex film-coated tablet

Package unit

28 tablets/box [(14 tablets/PTPX2)]

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.

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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.