Medication info
Sitagliptin 50 mg (Sitagliptin Hydrochloride Monohydrate) Tablet

Sitagliptin 50 mg (Sitagliptin Hydrochloride Monohydrate) Tablet

Prescription medicationTablet경구
Ingredient · strength
Sitagliptin Hydrochloride Hydrate›56.69mg / 1 tablet
Manufacturer / importer
신풍제약(주)
Appearance
Bright yellow-orange round film-coated tablet
Packaging
30 tablets/bottle, 100 tablets/bottle
Approval status
Active

MFDS item code 202102483 · Approved 2021.03.22 · Insurance code 648508090

Summary

Main use
Improves blood sugar control in type 2 diabetes
Who takes it
Adults
Adult dose
This medication is administered once a day at a dose of 100 mg for monotherapy or combination therapy, with a maximum allowable dose of 100 mg per day. It can be taken regardless of meals. In patients with renal impairment: - For mild to moderate renal impairment (eGFR ≥ 45 mL/min/1.73 m2), no dosage adjustment is necessary. - For moderate renal impairment (eGFR ≥ 30 and < 45 mL/min/1.73 m2), the dosage is 1

Ingredients

Manufacturer
신풍제약(주)

Efficacy & effects

Improves 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 combination with diet and exercise to enhance blood sugar control in patients with type 2 diabetes. It can be administered alone for those starting treatment for the first time, and if blood sugar is not adequately controlled with monotherapy, it is used in conjunction with metformin. Additionally, if blood sugar control is difficult with other diabetes medications such as sulfonylureas, metformin, thiazolidinediones, or insulin, this medication can be added. Even when using multiple medications, this drug can be used to enhance therapeutic effects if blood sugar control is insufficient. In summary, this medication plays an important role in aiding blood sugar control at various stages of diabetes treatment and can be used either alone or in combination based on the patient's condition to improve blood sugar management.

How to take

Adult dose

This medication is administered once a day at a dose of 100 mg for monotherapy or combination therapy, with a maximum allowable dose of 100 mg per day. It can be taken regardless of meals. In patients with renal impairment: - For mild to moderate renal impairment (eGFR ≥ 45 mL/min/1.73 m2), no dosage adjustment is necessary. - For moderate renal impairment (eGFR ≥ 30 and < 45 mL/min/1.73 m2), the dosage is 1

Precautions

This medication may cause serious allergic reactions after administration, so if symptoms such as rash or difficulty breathing occur, discontinue use immediately and consult a physician. There is also a risk of serious inflammation of the pancreas known as pancreatitis, so if symptoms like abdominal pain or vomiting arise, inform medical personnel promptly. This medication should not be used by patients with type 1 diabetes or diabetic ketoacidosis, nor in cases of hypersensitivity to this medication or its components. Patients with decreased renal function should have their dosage adjusted, hence regular renal function tests are necessary. During the course of this medication, hypoglycemic symptoms may occur, especially when taken with insulin or sulfonylureas, so blood sugar levels should be closely monitored. If severe joint pain or blisters on the skin occurs, notify a doctor immediately and discontinue the medication. Pregnant or nursing women are advised to avoid using this medication, and safety in children and adolescents under 18 years has not been established. Elderly individuals may have decreased renal function, so dosage adjustment and renal function testing is required. Be aware that interactions may occur when taken with other medications, so inform healthcare providers of any concurrent medications being taken. In the case of overdose, visit a hospital immediately for appropriate treatment, and this medication can be partially removed by dialysis.

Side effects and when to seek care immediately

Serious side effects

Urticaria, severe swelling (angioedema), chest tightness, difficulty breathing, anaphylaxis, severe hypersensitivity reactions, Stevens-Johnson syndrome (severe skin reactions), acute pancreatitis (life-threatening/non-life threatening hemorrhagic or necrotizing), dyspnea or difficulty breathing, asthma attack, yellowing of skin or eyes (jaundice), sudden and severe headache, seizures, consciousness disturbance, visual disturbances, paralysis, markedly reduced urine output

Mild side effects

  • Upper respiratory infection
  • nasopharyngitis
  • headache
  • diarrhea
  • abdominal pain
  • nausea
  • constipation
  • myalgia
  • limb pain
  • back pain
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  • pruritis
  • thrombocytopenia
  • dyspepsia
  • dizziness
  • increased plasma 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 closed container to prevent air or moisture exposure and kept at room temperature between 1 and 30 degrees Celsius. Proper storage will maintain the medication's effectiveness and ensure safe use.

Appearance and packaging

Appearance

Bright yellow-orange round film-coated tablet

Package unit

30 tablets/bottle, 100 tablets/bottle

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.