Medication info

Sitava Tablet 25 mg (Sitagliptin Hydrochloride Monohydrate)

Prescription medicationTablet경구Expired
Ingredient · strength
Sitagliptin Hydrochloride Hydrate›28.35mg / 1 tablet
Manufacturer / importer
(주)에이프로젠바이오로직스
Appearance
Pink, round, double convex film-coated tablet
Packaging
28 tablets) 14 tablets/PTP(x2), 30 tablets) 10 tablets/PTP(x3)
Approval status
Expired

MFDS item code 202004106 · Approved 2020.05.29

This product's status changed to Expired on 2025.05.29. 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
The recommended dose is 100 mg once daily, either as monotherapy or as part of combination therapy, with a maximum daily dose of 100 mg. It can be taken regardless of meals. For patients with renal impairment, dose adjustment is necessary. - Mild renal impairment (eGFR 60-90 mL/min/1.73 m2): No dose adjustment needed. - Moderate renal impairment (eGFR 45-60 mL/min/1.73 m2):

Ingredients

Manufacturer
(주)에이프로젠바이오로직스

Efficacy & effects

Improvement of blood sugar control in type 2 diabetes

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

This medication is used to help control blood sugar levels in patients with type 2 diabetes. It can be administered alone or in combination with dietary and exercise therapy, and if the monotherapy is insufficient during initial treatment, it is combined with metformin. Additionally, it can be used to enhance effectiveness in patients having difficulty with blood sugar control, whether administered alone or in combination with other diabetes medications such as sulfonylureas, thiazolidinediones, and insulin. This combination therapy helps to further improve blood sugar control.

How to take

Adult dose

The recommended dose is 100 mg once daily, either as monotherapy or as part of combination therapy, with a maximum daily dose of 100 mg. It can be taken regardless of meals. For patients with renal impairment, dose adjustment is necessary. - Mild renal impairment (eGFR 60-90 mL/min/1.73 m2): No dose adjustment needed. - Moderate renal impairment (eGFR 45-60 mL/min/1.73 m2):

Precautions

This medication can rarely cause serious allergic reactions. Such reactions may appear within the first 3 months after starting the medication, so if symptoms like skin rash or difficulty breathing occur, it is important to stop taking the drug immediately and consult a doctor. This medication can cause a disease known as pancreatitis, which is inflammation of the pancreas, so if symptoms like abdominal pain or vomiting occur, alert healthcare personnel immediately. This medication should not be used in patients with type 1 diabetes, diabetic ketoacidosis, or those allergic to this drug or its components. Patients with impaired kidney function may require a dose adjustment, and it is important to undergo regular kidney function tests. During treatment with this medication, symptoms similar to a cold, headache, indigestion, diarrhea may occur. Additionally, symptoms of hypoglycemia may appear, especially when taken with insulin or sulfonylureas, so caution is needed. The risk of hypoglycemia may increase when this medication is taken with other hypoglycemic agents; therefore, adjusting the doses of other medications may be necessary. Rarely, symptoms like arthralgia or blisters on the skin have been reported, so if these symptoms appear, consult a physician immediately. This medication is not recommended for use during pregnancy or breastfeeding, and its safety for children under 18 years old has not been established. In cases of overdose, general supportive care and, if necessary, blood dialysis may be considered. This medication is known not to significantly affect cardiovascular safety; however, if any abnormal symptoms occur during treatment, consult a healthcare provider immediately.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (angioedema), chest tightness, difficulty breathing, severe hypersensitivity reactions (anaphylaxis), severe skin reactions (Stevens-Johnson syndrome, exfoliative skin disease), acute pancreatitis, worsening kidney function (acute renal failure), severe joint pain with disability, bullous pemphigoid, severe allergic reactions, significant swelling, liver abnormalities (elevated liver enzymes), angioedema, severe neurological symptoms (including cardiac arrest)

Mild side effects

  • Headache
  • upper respiratory infection
  • nasopharyngitis
  • diarrhea
  • nausea
  • abdominal pain
  • constipation
  • vomiting
  • pruritus
  • myalgia
Show 12 more
  • limb pain
  • back pain
  • thrombocytopenia
  • indigestion
  • dizziness
  • increased blood triglycerides
  • increased low-density lipoprotein
  • hyperglycemia
  • weight loss
  • hypertension
  • hypernatremia
  • erectile dysfunction

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

Storage

This medication should be stored in a tightly closed container to protect it from air or moisture, and it is best to keep it at room temperature between 1 and 30 degrees Celsius. Storing it this way helps maintain the effectiveness of the medication for a longer time.

Appearance and packaging

Appearance

Pink, round, double convex film-coated tablet

Package unit

28 tablets) 14 tablets/PTP(x2), 30 tablets) 10 tablets/PTP(x3)

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.