Medication info
Miarilem Tablets 2/500 mg

Miarilem Tablets 2/500 mg

Prescription medicationTablet경구
Ingredient · strength
Metformin Hydrochloride›500mg / 1 tabletGlimepiride›2mg / 1 tablet
Manufacturer / importer
진양제약(주)
Appearance
White elongated film-coated tablet
Packaging
30 tablets per bottle, 300 tablets per bottle
Approval status
Active

MFDS item code 201107201 · Approved 2011.09.27 · Insurance code 650302810

Summary

Main use
Improvement of blood sugar control in type 2 diabetes
Who takes it
Adults
Adult dose
This medication should be taken once or twice a day before meals or with meals. The dosage may be adjusted considering each patient's current treatment regimen, efficacy, and tolerance, necessitating appropriate blood sugar monitoring. Typically, treatment starts at a low dose, and adjustments can be made considering the patient's current medications and blood sugar levels. In clinical trials, the initial daily dose was Glimepiride/Metformin Hydrochloride 2 mg/500 mg, and the dose has been gradually increased to Glimepiride/Metformin Hydrochloride 8 mg/2000 mg based on blood sugar monitoring results. The single-agent Glimepiride generally shows little additional effect at doses above 4 mg per day; however, some patients have shown better metabolic control with doses increased up to 6 mg (or 8 mg). When used as an alternative therapy in combination treatment, dosing should be based on the current regimen of Glimepiride and Metformin Hydrochloride. In case a dose is missed, do not exceed the prescribed dose at the next interval.

Ingredients

Manufacturer
진양제약(주)

Efficacy & effects

Improvement of blood sugar control in type 2 diabetes

View approved original text

This medication is used in conjunction with dietary management and exercise therapy to help control blood sugar levels in patients with type 2 diabetes. The combination administration of Glimepiride and Metformin allows for more effective management of blood sugar levels. This contributes to stabilizing blood sugar levels in patients and assists in diabetes treatment.

How to take

Adult dose

This medication should be taken once or twice a day before meals or with meals. The dosage may be adjusted considering each patient's current treatment regimen, efficacy, and tolerance, necessitating appropriate blood sugar monitoring. Typically, treatment starts at a low dose, and adjustments can be made considering the patient's current medications and blood sugar levels. In clinical trials, the initial daily dose was Glimepiride/Metformin Hydrochloride 2 mg/500 mg, and the dose has been gradually increased to Glimepiride/Metformin Hydrochloride 8 mg/2000 mg based on blood sugar monitoring results. The single-agent Glimepiride generally shows little additional effect at doses above 4 mg per day; however, some patients have shown better metabolic control with doses increased up to 6 mg (or 8 mg). When used as an alternative therapy in combination treatment, dosing should be based on the current regimen of Glimepiride and Metformin Hydrochloride. In case a dose is missed, do not exceed the prescribed dose at the next interval.

Precautions

This drug may cause severe lactic acidosis or hypoglycemia, so special care should be taken in situations where kidney function rapidly deteriorates. If symptoms of dehydration occur, it is advisable to temporarily discontinue this drug and consult a physician. When used with medications that can cause acute renal impairment, renal function should be closely monitored. In patients with cardiovascular diseases, the use of this drug may increase the risk of cardiovascular mortality, so caution is required. This drug is not to be administered to patients with insulin-dependent diabetes, acute metabolic acidosis, severe liver or kidney dysfunction, pregnant or breastfeeding women. Additionally, administration of this drug should be temporarily suspended before and after tests using radiographic contrast agents, and it should be resumed only after renal function has stabilized. Patients at high risk for hypoglycemia, malnutrition, and those with high alcohol intake require dosage adjustments and careful monitoring. Gastrointestinal side effects (such as diarrhea, nausea, vomiting, etc.) may occur initially but are mostly temporary and can be alleviated by taking the medication with food. Rarely, vitamin B12 deficiency may occur, so regular blood testing is recommended during long-term use. This drug may interact with other medications, so it is essential to inform a physician or pharmacist of any other medications being taken. Caution is needed when driving or operating machinery due to the potential for hypoglycemia or dexterity impairment. In case of overdose, symptoms of hypoglycemia may occur, and immediate medical attention should be sought. This drug requires careful observation and dosage adjustments when used in children or the elderly. It is important to regularly monitor blood sugar levels and renal function to confirm the efficacy and safety of treatment.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (edema), difficulty breathing, drop in blood pressure, shock, liver dysfunction (jaundice), hepatitis, liver failure, severe hypoglycemia, coma, loss of consciousness, severe allergic reaction, lactic acidosis, acute renal failure, serious thrombocytopenia with thrombocytopenic purpura, cardiac arrest, rectal cancer, encephalopathy, severe rash, blisters, skin peeling, pain in oral/ocular mucosa, headache, thunderclap headache, seizure, confusional state, visual disturbances

Mild side effects

Diarrhea, nausea, vomiting, abdominal bloating, loss of appetite, dyspepsia, constipation, abdominal pain, sensation of fullness or pressure in the upper abdomen, taste disorder, malaise, metallic taste, visual impairment, erythema, itching, rash, thrombocytopenia, leukopenia, hemolytic anemia, erythrocytopenia, agranulocytosis, pancytopenia, vitamin B12 reduction, increased liver enzymes, liver function impairment, hepatitis, allergic vasculitis, photosensitivity of the skin,

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

Storage

This drug should be stored in a tightly sealed container to prevent air entry, at room temperature between 1 degree and 30 degrees Celsius. This will help maintain the drug's efficacy for an extended period.

Appearance and packaging

Appearance

White elongated film-coated tablet

Package unit

30 tablets per bottle, 300 tablets per 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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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.