Medication info
Glycita Tablet 50 mg (Sitagliptin Hydrochloride Hydrate)

Glycita Tablet 50 mg (Sitagliptin Hydrochloride Hydrate)

Prescription medicationTablet
Ingredient · strength
Sitagliptin Hydrochloride Hydrate›56.7mg / 1 tablet
Manufacturer / importer
(주)동구바이오제약
Appearance
Light apricot colored, biconvex, round, film-coated tablets
Packaging
28 tablets/box [14 tablets/PTPX2]
Approval status
Active

MFDS item code 202102395 · Approved 2021.03.17 · Insurance code 657308540

Summary

Main use
Improvement of blood sugar control in type 2 diabetes
Who uses it
Adults
Adult dosage
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 can be taken without regard to meals. For patients with renal impairment, dose adjustment is necessary according to kidney function. 1. For mild renal impairment (eGFR 60-90 mL/min/1.73 m2), no dose adjustment is necessary. 2. For moderate renal impairment (eGFR 45-60 mL/min/1.73 m2), dose adjustment is not required.

Ingredients

Manufacturer
(주)동구바이오제약

Efficacy & effects

Improvement of blood sugar control in type 2 diabetes

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

This medication is used to control blood sugar in patients with type 2 diabetes. Initially, it can be administered alone in conjunction with dietary and exercise therapy. If blood sugar control is insufficient, it can be used in combination with metformin. Additionally, if controlling blood sugar remains difficult despite using other diabetes medications such as sulfonylureas, thiazolidinediones, and insulin, this medication may be added to the treatment regimen. This helps improve blood sugar control.

Dosage and Administration

Adult dosage

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 can be taken without regard to meals. For patients with renal impairment, dose adjustment is necessary according to kidney function. 1. For mild renal impairment (eGFR 60-90 mL/min/1.73 m2), no dose adjustment is necessary. 2. For moderate renal impairment (eGFR 45-60 mL/min/1.73 m2), dose adjustment is not required.

Precautions

This medication may cause severe hypersensitivity reactions after administration, so if allergy symptoms are suspected, use should be discontinued immediately. Symptoms of serious pancreatic issues such as acute pancreatitis may appear, so caution is advised for symptoms such as abdominal pain or vomiting. This medication should not be used in patients with type 1 diabetes or diabetic ketoacidosis, nor should it be administered to patients allergic to this medication or any of its ingredients. Dose adjustment is necessary for patients with reduced kidney function, so regular kidney function tests should be conducted. Reported side effects in clinical trials include upper respiratory infections, headaches, nasopharyngitis, dyspepsia, diarrhea, and hypoglycemic symptoms may also occur. When taken with other blood sugar lowering agents, especially insulin or sulfonylureas, there is an increased risk of hypoglycemia, so caution is required. Severe adverse reactions such as serious joint pain or skin blisters may occur, and if these symptoms appear, immediate consultation with healthcare professionals is necessary. It is preferable for women who are pregnant or breastfeeding not to take this medication, and the safety of this medication for children and adolescents under 18 years of age has not been established. In the case of overdose, general treatment should be administered, and if necessary, hemodialysis can be performed to remove the drug. This medication does not pose safety concerns regarding cardiovascular effects, and it can be used relatively safely in elderly individuals, although kidney function status should be monitored regularly.

Side effects and when to seek care immediately

Serious side effects

Urticaria, severe hypersensitivity reaction (anaphylaxis, angioedema), Stevens-Johnson syndrome, cutaneous vasculitis, severe skin adverse reactions (rash, exfoliative skin disease), acute pancreatitis (fatal/non-fatal hemorrhagic or necrotizing), acute renal failure, severe and disabling arthralgia, bullous pemphigoid, rhabdomyolysis, anaphylaxis, angioedema, chest tightness, difficulty breathing, cold sweat, pallor, high fever accompanied by severe

Mild side effects

  • Nasopharyngitis
  • upper respiratory infection
  • headache
  • constipation
  • vomiting
  • myalgia
  • limb pain
  • back pain
  • pruritus
  • thrombocytopenia
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  • diarrhea
  • abdominal pain
  • nausea
  • dyspepsia
  • dizziness
  • increased serum triglycerides
  • gastritis
  • 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 sealed container to prevent air exposure and maintained at a temperature between 1 to 30 degrees Celsius for safety. Storing it this way will help maintain the medication's effectiveness.

Appearance and packaging

Appearance

Light apricot colored, biconvex, round, film-coated tablets

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.

Questions about this medicine

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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.