Medication info
Janumet 25 mg (Sitagliptin Hydrochloride Monohydrate)

Janumet 25 mg (Sitagliptin Hydrochloride Monohydrate)

Prescription medicationTablet
Ingredient · strength
Sitagliptin Hydrochloride Hydrate›28.35mg / 1 tablet
Manufacturer / importer
에이치엘비제약(주)
Appearance
Pink, round, biconvex, film-coated tablet
Packaging
28 tablets/box [14 tablets/PTP×2]
Approval status
Active

MFDS item code 202101226 · Approved 2021.02.10 · Insurance code 647304470

Summary

Main use
Improvement of blood sugar control in type 2 diabetes
Who uses it
Adults
Adult dosage
The recommended dose is 100 mg once daily for either monotherapy or in combination therapy, with a maximum daily dose of 100 mg. For patients with moderate renal impairment (glomerular filtration rate [eGFR] 30–45 mL/min/1.73 m2), the dose is reduced to 50 mg once daily. For patients with severe renal impairment (glomerular filtration rate [eGFR] 15–30 mL/min/1.73 m2) or end-stage renal disease (glomerular filtration rate [eGFR] < 15 mL/min/1.73 m2), additional dose adjustments are made.

Ingredients

Manufacturer
에이치엘비제약(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 to improve blood sugar control in patients with type 2 diabetes. It is primarily administered in conjunction with dietary modifications and exercise, and can also be used as monotherapy. If there is no prior experience with diabetes treatment and blood sugar control is difficult with monotherapy, it is used in combination with metformin. Additionally, when the blood sugar control is insufficient with any one of sulfonylureas, metformin, thiazolidinediones, or insulin, this medication is added. In cases where blood sugar control is difficult even with various combination therapies, this medication is used to enhance treatment efficacy. Thus, it effectively improves blood sugar control in various situations.

Dosage and Administration

Adult dosage

The recommended dose is 100 mg once daily for either monotherapy or in combination therapy, with a maximum daily dose of 100 mg. For patients with moderate renal impairment (glomerular filtration rate [eGFR] 30–45 mL/min/1.73 m2), the dose is reduced to 50 mg once daily. For patients with severe renal impairment (glomerular filtration rate [eGFR] 15–30 mL/min/1.73 m2) or end-stage renal disease (glomerular filtration rate [eGFR] < 15 mL/min/1.73 m2), additional dose adjustments are made.

Precautions

This medication may cause serious allergic reactions such as skin rash, anaphylaxis, and angioedema, so caution is needed. If symptoms of pancreatitis, such as abdominal pain, vomiting, or persistent abdominal discomfort occur during the use of this medication, consult a healthcare professional immediately. It should not be used by patients with type 1 diabetes, diabetic ketoacidosis, or those with hypersensitivity to this medication or its components. Patients with impaired kidney function should have their dosage adjusted, and regular monitoring of kidney function is important. Low blood sugar symptoms may occur while using this medication; therefore, glucose levels should be carefully monitored, especially when taken with insulin or sulfonylureas. This medication may cause side effects such as headache, upper respiratory tract infections, nasopharyngitis, diarrhea, nausea, etc., so report to a healthcare professional if symptoms are severe. If severe joint pain or symptoms resembling bullous pemphigoid occurs, immediately discontinue use and consult a healthcare professional. Pregnant or nursing women should avoid taking this medication, and safety in children and adolescents under 18 years of age has not been established. In the event of overdose, seek appropriate treatment at a hospital immediately, as this medication can be partially removed through hemodialysis. This medication has minimal drug interactions, but consult a healthcare professional when used in conjunction with specific medications. Elderly patients may have a reduced kidney function, so dosage adjustments and regular kidney function assessments are necessary.

Side effects and when to seek care immediately

Serious side effects

Urticaria, severe swelling (angioedema), anaphylaxis, rash, severe skin reactions (Stevens-Johnson syndrome, exfoliative skin disease), acute pancreatitis, difficulty breathing, severe hypoglycemia, severe joint pain, bullous pemphigoid, liver abnormalities (increased liver enzymes, jaundice), acute renal failure, severe neurological symptoms (including cardiac arrest)

Mild side effects

  • Upper respiratory infection
  • nasopharyngitis
  • constipation
  • vomiting
  • headache
  • muscle pain
  • limb pain
  • back pain
  • pruritus
  • thrombocytopenia
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  • diarrhea
  • abdominal pain
  • nausea
  • dyspepsia
  • dizziness
  • increased serum triglycerides
  • hypertension
  • weight loss
  • hypernatremia
  • erectile dysfunction

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

Storage

Store this medication in a tightly sealed container to prevent air exposure and keep it at room temperature between 1 and 30 degrees Celsius. Storing it this way helps maintain the drug's efficacy for a longer time.

Appearance and packaging

Appearance

Pink, round, biconvex, film-coated tablet

Package unit

28 tablets/box [14 tablets/PTP×2]

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.