Medication info

Janusita Tablet 50 mg (Sitagliptin Phosphate)

Prescription medicationTablet경구Expired
Ingredient · strength
Sitagliptin Phosphate›62.04mg / 1 tablet
Manufacturer / importer
제일약품(주)
Appearance
Bright beige, bilaterally convex, round film-coated tablet
Packaging
30 tablets/box [10 tablets/PTPX3 units]
Approval status
Expired

MFDS item code 201503269 · Approved 2015.05.28

This product's status changed to Expired on 2025.05.28. 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 at a dose of 100 mg once daily, whether used alone or in combination, with a maximum daily dose of 100 mg. It can be taken regardless of meals. Dosage adjustment based on kidney function is necessary. - No dosage adjustment is needed for patients with mild renal impairment. - For patients with moderate renal impairment (glomerular filtration rate of 30–45 mL/min/1.73 m2), administer 50 mg once daily. - For severe renal impairment (glomerular filtration rate of

Ingredients

Manufacturer
제일약품(주)

Efficacy & effects

Improvement of blood sugar control in type 2 diabetes

  • Type 2 diabetes
  • difficulty in blood sugar control
View approved original text

This medication is used to aid in blood sugar control for patients with type 2 diabetes. Initially, it can be administered alone in combination with dietary and exercise therapy. If sufficient blood sugar control is difficult with monotherapy, it can be used in conjunction with metformin. Additionally, it can be administered in combination with other antidiabetic medications such as sulfonylureas, metformin, thiazolidinediones, and insulin. When blood sugar control is challenging with multiple drug combination therapy, this medication can be added to improve blood sugar control. This medication enhances blood sugar management in patients with type 2 diabetes at various treatment stages.

How to take

Adult dose

This medication is administered at a dose of 100 mg once daily, whether used alone or in combination, with a maximum daily dose of 100 mg. It can be taken regardless of meals. Dosage adjustment based on kidney function is necessary. - No dosage adjustment is needed for patients with mild renal impairment. - For patients with moderate renal impairment (glomerular filtration rate of 30–45 mL/min/1.73 m2), administer 50 mg once daily. - For severe renal impairment (glomerular filtration rate of

Precautions

This medication may cause severe hypersensitivity reactions, so if symptoms such as skin rash, angioedema, or difficulty breathing occur within 3 months after administration, usage should be immediately discontinued and medical attention sought. Acute pancreatitis may occur during the use of this drug; therefore, if symptoms such as abdominal pain, vomiting, or persistent abdominal discomfort appear, medical personnel should be informed immediately. This drug should not be used in patients with type 1 diabetes or diabetic ketoacidosis. Patients with hypersensitivity to this drug or its components should not take it. Patients with decreased kidney function may need dosage adjustment; it is important to perform kidney function tests before administration. Hypoglycemia symptoms may occur while taking this drug, so blood sugar should be monitored regularly, especially when taken with insulin or sulfonylureas. Severe joint pain or blistering skin conditions may arise; consult a physician immediately if such symptoms occur. It is safer for pregnant or breastfeeding women not to take this drug. Elderly patients may have reduced kidney function, requiring dosage adjustments and kidney function testing. In case of overdose, immediate hospital visit for appropriate treatment is necessary; this drug can be partially removed by hemodialysis. Due to the potential for drug interactions, inform your doctor or pharmacist if you are currently taking any medications.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, anaphylaxis, angioedema, severe allergic reactions, severe rash with fever, blisters, skin peeling, mucosal pain in mouth/eyes, Stevens-Johnson syndrome, severe skin adverse reactions, shortness of breath or difficulty breathing, asthma attack, respiratory issues accompanied by cough and fever, liver abnormalities (jaundice), yellowing of skin or eyes, extreme fatigue

Mild side effects

  • Upper respiratory tract infection
  • nasopharyngitis
  • constipation
  • vomiting
  • headache
  • myalgia
  • limb pain
  • back pain
  • pruritus
  • thrombocytopenia
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  • dyspepsia
  • dizziness
  • diarrhea
  • nausea
  • increase in blood triglycerides
  • increase in low-density lipoprotein
  • hyperglycemia
  • weight loss
  • hypernatremia
  • erectile dysfunction

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

Storage

This medication should be stored in an airtight closed container, kept at room temperature between 1 degree and 30 degrees Celsius. Proper storage will help maintain the effectiveness of the drug.

Appearance and packaging

Appearance

Bright beige, bilaterally convex, round film-coated tablet

Package unit

30 tablets/box [10 tablets/PTPX3 units]

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.