Medication info
Esriptin M Tablet 50/500 mg

Esriptin M Tablet 50/500 mg

Prescription medicationTablet경구
Ingredient · strength
Sitagliptin Hydrochloride Hydrate›56.7mg / 1 tabletMetformin Hydrochloride with Colloidal Anhydrous Silica›505mg / 1 tablet
Manufacturer / importer
위더스제약(주)
Appearance
Bright pink oval film-coated tablet
Packaging
30 tablets/box [10 tablets/PTP X 3]
Approval status
Active

MFDS item code 202200334 · Approved 2022.01.20 · Insurance code 660703810

Summary

Main use
Improvement of blood sugar control in type 2 diabetes
Who takes it
Adults
Adult dose
This medication is generally taken twice a day with food, and the dosage is gradually increased to reduce gastrointestinal side effects caused by metformin. 1. For patients not currently receiving treatment with metformin: Take this medication 50/500 mg twice a day, one tablet at a time; the dosage can be increased to 50/1000 mg twice a day, one tablet at a time. 2. For patients already on metformin treatment: Sitagliptin

Ingredients

Manufacturer
위더스제약(주)

Efficacy & effects

Improvement of blood sugar control in type 2 diabetes

  • Difficulty in blood glucose control 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 used as an alternative when blood sugar control is inadequate with monotherapy of metformin or sitagliptin, or when these two medications are used together. Additionally, it can be used alongside metformin in cases where blood sugar control is difficult in combination with sulfonylurea, or when combined with thiazolidinedione therapy with metformin. If combination therapy with insulin and metformin is not effective, this medication may also be used to enhance therapeutic effects. It is used to improve blood sugar control alongside dietary management and exercise.

How to take

Adult dose

This medication is generally taken twice a day with food, and the dosage is gradually increased to reduce gastrointestinal side effects caused by metformin. 1. For patients not currently receiving treatment with metformin: Take this medication 50/500 mg twice a day, one tablet at a time; the dosage can be increased to 50/1000 mg twice a day, one tablet at a time. 2. For patients already on metformin treatment: Sitagliptin

Precautions

This medication contains sitagliptin and metformin, and is primarily used for the treatment of type 2 diabetes. The sitagliptin component may cause severe hypersensitivity reactions, skin disorders, or acute pancreatitis in some patients, so if these symptoms occur within 3 months after starting treatment, consult a physician immediately. The metformin component can cause a rare yet potentially fatal side effect called lactic acidosis, and should not be used in patients with impaired kidney function or liver dysfunction. Especially, it should not be administered to patients with moderate to severe renal impairment, acute heart failure, or acute myocardial infarction, as well as to patients with severe infections or dehydration, and administration should also be discontinued around the time of diagnostic tests using iodine contrast agents. It is not recommended for use in pregnant women or those who may become pregnant, nursing mothers, or children under 18 years of age. While taking this medication, be cautious of hypoglycemic symptoms when using other medications that may cause blood sugar lowering, particularly when used in combination with insulin or sulfonylureas, as the risk of hypoglycemia may increase. Moreover, patients engaging in vigorous exercise or those with irregular eating habits or nutritional imbalances should be particularly cautious while taking this medication. Regular monitoring of kidney function and blood tests should be performed while taking this medication, and since vitamin B12 levels may decline, supplementation may be necessary if needed. Alcohol consumption may increase the risk of lactic acidosis, so excessive drinking should be avoided while taking this medication. In cases of undergoing surgery or when oral intake is restricted, this medication should be temporarily discontinued 48 hours prior to surgery and can be resumed only after confirming normal kidney function post-recovery. Patients taking this medication should immediately inform healthcare providers and discontinue use if they notice any unusual symptoms such as skin rash, hives, difficulty breathing, sudden joint pain, or blistering skin conditions. In the event of overdose, general symptomatic treatment may be provided along with dialysis if necessary. Although clinical trials have confirmed that this medication does not increase the risk of cardiovascular diseases, caution is warranted based on the patient’s condition. Therefore, this medication should be taken precisely according to the physician's prescription and instructions, and immediate consultation with healthcare providers should be sought if any unusual symptoms arise.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (angioedema), chest tightness, difficulty breathing, anaphylaxis, Stevens-Johnson syndrome, skin rash, skin peeling, pain in oral/ocular mucosa, acute pancreatitis, acute kidney failure, elevated liver enzymes, thrombocytopenia, severe neurological symptoms (severe headache, confusion, visual disturbances, paralysis), hypoglycemia (severe), lactic acidosis, respiratory distress, unstable angina, acute myocardial infarction, sepsis, acute heart failure,

Mild side effects

  • Diarrhea
  • upper respiratory infection
  • headache
  • nausea
  • vomiting
  • abdominal pain
  • constipation
  • nasopharyngitis
  • muscle pain
  • limb pain
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  • back pain
  • pruritus
  • thrombocytopenia
  • decreased appetite
  • itching
  • dizziness
  • decreased serum B12 levels
  • anemia
  • bullous pemphigoid
  • severe and disabling arthralgia

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

Storage

This medication should be stored in a tightly sealed container that is well-ventilated and kept at room temperature between 1 to 30 degrees Celsius. Proper storage helps maintain the medication's effectiveness for a longer period.

Appearance and packaging

Appearance

Bright pink oval film-coated tablet

Package unit

30 tablets/box [10 tablets/PTP X 3]

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.