Medication info
Bearyl M Tablet 2/500mg (Glibenclamide, Metformin Hydrochloride)

Bearyl M Tablet 2/500mg (Glibenclamide, Metformin Hydrochloride)

Prescription medicationTablet경구
Ingredient · strength
Metformin Hydrochloride›500mg / 1 tabletGlimepiride›2mg / 1 tablet
Manufacturer / importer
대웅바이오(주)
Appearance
White oblong film-coated tablet
Packaging
30 tablets/bottle, 100 tablets/bottle
Approval status
Active

MFDS item code 201301375 · Approved 2013.01.15 · Insurance code 694000490

Summary

Main use
Improvement of blood sugar control in type 2 diabetes
Who takes it
Adults
Adult dose
This medication is administered 1-2 times a day before meals or with meals. The dosage can be adjusted considering the patient’s current treatment regimen, efficacy, and tolerability, with appropriate blood sugar monitoring. Treatment usually begins at a low dose, and the dosage can be adjusted based on the patient’s current medications and blood sugar levels. In clinical trials, the initial daily dosage was Glibenclamide/Metformin Hydrochloride 2mg/

Ingredients

Manufacturer
대웅바이오(주)

Efficacy & effects

Improvement of blood sugar control in type 2 diabetes

View approved original text

This medication is used to assist diet and exercise for the control of blood sugar in patients with type 2 diabetes. It contains Glibenclamide and Metformin to effectively lower blood sugar levels. Therefore, it is used to improve diabetes symptoms through blood sugar management.

How to take

Adult dose

This medication is administered 1-2 times a day before meals or with meals. The dosage can be adjusted considering the patient’s current treatment regimen, efficacy, and tolerability, with appropriate blood sugar monitoring. Treatment usually begins at a low dose, and the dosage can be adjusted based on the patient’s current medications and blood sugar levels. In clinical trials, the initial daily dosage was Glibenclamide/Metformin Hydrochloride 2mg/

Precautions

This medication can cause severe lactic acidosis or hypoglycemia, so it should be discontinued if renal function rapidly declines. It is important to temporarily stop taking this medication and consult a doctor if there are symptoms of dehydration. Caution should be exercised when taking this medication together with other drugs that can cause acute renal failure. Excessive alcohol consumption, liver dysfunction, and poorly controlled diabetes can also increase the risk of side effects with this medication. Patients and caregivers must be thoroughly educated about the risks and symptoms of lactic acidosis, and if symptoms occur, they should immediately stop taking the medication and seek emergency care. Renal function should be evaluated before starting treatment and regularly thereafter; this medication is not used in patients with reduced kidney function. This medication should not be administered to patients with insulin-dependent diabetes, acute metabolic acidosis, severe liver dysfunction, pregnant or breastfeeding women, or those with severe kidney impairment. Patients at high risk for hypoglycemia, those in a state of malnutrition, elderly patients, and patients with liver dysfunction should use this medication with caution and carefully monitor for symptoms of hypoglycemia. This medication may cause gastrointestinal disturbances, allergic reactions, hematological abnormalities, vitamin B12 deficiency, and other side effects, so consult a doctor immediately if abnormal symptoms occur. Regularly check blood sugar control status and be cautious about potential interactions with other medications. In particular, when used in combination with drugs that affect renal function, kidney function should be monitored, and treatment should be temporarily suspended in cases of acute illness or surgery. Patients who are pregnant or planning to become pregnant should switch to insulin therapy instead of this medication, and breastfeeding women should avoid administration as well. Dosing and administration for children and elderly individuals should be determined cautiously, with special attention to reduced kidney function in the elderly. In case of overdose, hypoglycemia or lactic acidosis may occur, so inform medical personnel immediately and receive appropriate treatment. While taking this medication, it is important to maintain a regular diet and exercise regimen, as well as consistently perform blood sugar and kidney function tests. Special care is needed while driving or operating machinery due to the risk of accidents from hypoglycemia or hyperglycemia. Keep this medication out of reach of children and do not transfer it to another container.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), cardiac arrest, headaches, seizures, confusion, visual disturbances, paralysis, platelet count below 10,000/μL and thrombocytopenic purpura, yellowing of the skin or eyes (jaundice), liver failure, lactic acidosis, severe hypoglycemia, difficulty breathing, respiratory distress, asthma attacks, breathing difficulties accompanied by coughing and fever, markedly reduced urine output, severe systemic edema, elevated blood pressure

Mild side effects

  • Nausea
  • vomiting
  • abdominal distension
  • loss of appetite
  • indigestion
  • constipation
  • abdominal pain
  • taste disorders
  • thrombocytopenia
  • leukopenia
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  • hemolytic anemia
  • anemia
  • granulocytopenia
  • agranulocytosis
  • pancytopenia
  • vitamin B12 reduction
  • increased liver enzymes
  • liver function impairment
  • hepatitis
  • allergic vasculitis
  • photosensitivity
  • decreased serum sodium concentration
  • hypothyroidism
  • magnesium deficiency in diarrhea
  • encephalopathy
  • hair loss
  • weight change

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 and moisture from entering. The appropriate storage temperature is between 1 to 30 degrees Celsius at room temperature. By storing this medication in this manner, its effectiveness can be maintained for a long time.

Appearance and packaging

Appearance

White oblong 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.