Medication info

New Glipfield M Tablet

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

MFDS item code 201603557 · Approved 2016.06.17

Summary

Main use
Improvement in blood sugar control for type 2 diabetes
Who takes it
Adults
Adult dose
This medication is administered 1-2 times a day just before or with meals. The initial dosage is glimepiride/metformin hydrochloride 2mg/500mg, and it can be gradually increased up to 8mg/2000mg based on blood glucose monitoring results. Generally, single-agent glimepiride shows minimal additional effects when doses beyond 4mg per day are used, although some patients may increase the dosage up to 6mg (or 8mg).

Ingredients

Manufacturer
안국뉴팜(주)

Efficacy & effects

Improvement in blood sugar control for type 2 diabetes

View approved original text

This medication is used to assist in the blood sugar control of patients with type 2 diabetes by using glimepiride and metformin together. Taking this medication alongside dietary management and exercise can effectively manage blood sugar levels. This helps in the treatment of diabetes and enhances the patient's health management.

How to take

Adult dose

This medication is administered 1-2 times a day just before or with meals. The initial dosage is glimepiride/metformin hydrochloride 2mg/500mg, and it can be gradually increased up to 8mg/2000mg based on blood glucose monitoring results. Generally, single-agent glimepiride shows minimal additional effects when doses beyond 4mg per day are used, although some patients may increase the dosage up to 6mg (or 8mg).

Precautions

This medication can cause severe lactic acidosis or hypoglycemia, so it should be temporarily discontinued, especially when there is a rapid decline in kidney function or dehydration. It is contraindicated in patients with a renal function of less than 45 mL/min/1.73m², and elderly patients or those in situations where renal function may worsen should have their renal function regularly assessed. The risk of cardiovascular disease may increase during the administration of this medication, so it is essential to thoroughly explain the benefits and risks of treatment to the patient and observe them carefully. It should not be used in patients with insulin-dependent diabetes, acute metabolic acidosis, severe liver dysfunction, pregnant or breastfeeding women, and patients with severe renal impairment. Patients at high risk for hypoglycemia, such as those with poor nutritional status, irregular eating habits, the elderly, and those with liver dysfunction, require special precautions while taking this medication. In the initial stages of treatment, gastrointestinal symptoms (diarrhea, nausea, vomiting, etc.) may appear, which are mostly temporary, but if symptoms are severe, consultation with a physician is necessary. Allergic reactions, hematological abnormalities, and symptoms of vitamin B12 deficiency may occur, so regular blood tests and monitoring of vitamin B12 levels are recommended. This medication may interact with other drugs, so patients must inform healthcare professionals of any medications they are taking, particularly medications that may affect renal function. If pregnant or planning to become pregnant, it is safer to switch to insulin therapy instead of using this medication. In cases of overdose, hypoglycemia or lactic acidosis may occur, requiring immediate emergency treatment, and, if necessary, drug removal by hemodialysis may be needed. Care should be taken when driving or operating machinery as hypoglycemia or impaired agility may occur. The safety and efficacy of this medication have not been established in children and adolescents, so it is advisable not to use it in children under 10 years old. During storage, keep it in a tightly sealed container away from the reach of children, and do not transfer it to other containers.

Side effects and when to seek care immediately

Serious side effects

Urticaria, dyspnea, severe edema, chest tightness, hypotension, severe allergic reactions, severe lactic acidosis, acute renal failure, jaundice due to liver dysfunction, liver failure, severe skin adverse reactions (severe rash, blisters, skin peeling, pain in oral/eye mucosa), cardiovascular abnormalities (history of cardiac arrest, myocardial infarction), severe hypoglycemia (cerebral seizures, consciousness confusion, coma), paralysis, visual disturbances, severe neurological symptoms.

Mild side effects

Gastrointestinal symptoms (diarrhea, nausea, vomiting, abdominal bloating, anorexia, dyspepsia, constipation, abdominal pain), taste disorders, temporary visual impairment due to changes in blood sugar levels, thrombocytopenia, leukopenia, hemolytic anemia, erythrocytopenia, granulocytopenia, agranulocytosis, pancytopenia, vitamin B12 decrease and deficiency, increased liver enzymes, liver function impairment, hepatitis, allergic vasculitis, skin photosensitivity, decreased serum sodium concentration.

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

Storage

This medication should be stored in a sealed container that prevents air or moisture from entering. Additionally, it is best to store the medication at room temperature, avoiding extremes of heat or cold, specifically between 1°C and 30°C.

Appearance and packaging

Appearance

White rectangular film-coated tablets

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.

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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.