Medication info
Newmet 500 mg (Metformin Hydrochloride)

Newmet 500 mg (Metformin Hydrochloride)

Prescription medicationTablet
Ingredient · strength
Metformin Hydrochloride›500mg / 1 tablet
Manufacturer / importer
하나제약(주)
Appearance
White, round film-coated tablet
Packaging
300 tablets/bottle
Approval status
Active

MFDS item code 201901971 · Approved 2019.04.01 · Insurance code 657806480

Summary

Main use
Improvement of type 2 diabetes (blood sugar control)
Who uses it
Adults · Children
Adult dosage
The adult dosage should be determined based on individual drug effects and tolerability, and should not exceed the maximum dose per day. Administer 500 mg 2-3 times daily with meals. Dosage should be increased gradually by 500 mg weekly, and if administering up to 2000 mg, it should generally be divided into two doses in the morning and evening. If exceeding 2000 mg, it should be taken three times a day with meals, and the maximum dose is 2550 mg.
Children's dosage
Children aged 10 years and older and adolescents should be given 500 mg once daily during or after meals. After one week, blood sugar levels should be measured and the dosage adjusted, with the maximum daily dose being 2000 mg.

Ingredients

Manufacturer
하나제약(주)

Efficacy & effects

Improvement of type 2 diabetes (blood sugar control)

  • Type 2 diabetes
  • blood sugar control issues
  • overweight
View approved original text

This drug is used in patients with type 2 diabetes who are not adequately controlled by diet and exercise, particularly in overweight adults and children and adolescents aged 10 years or older. In adults, it can be used alone or in combination with other oral hypoglycemic agents and insulin. Children and adolescents may also use it alone or in combination with insulin for effective blood sugar control. This helps to stabilize blood sugar levels and aids in diabetes treatment.

Dosage and Administration

Adult dosage

The adult dosage should be determined based on individual drug effects and tolerability, and should not exceed the maximum dose per day. Administer 500 mg 2-3 times daily with meals. Dosage should be increased gradually by 500 mg weekly, and if administering up to 2000 mg, it should generally be divided into two doses in the morning and evening. If exceeding 2000 mg, it should be taken three times a day with meals, and the maximum dose is 2550 mg.

Children's dosage

Children aged 10 years and older and adolescents should be given 500 mg once daily during or after meals. After one week, blood sugar levels should be measured and the dosage adjusted, with the maximum daily dose being 2000 mg.

Precautions

This drug can cause severe lactic acidosis or hypoglycemia, so caution is required. It should not be administered to patients with moderate or severe renal impairment, or those in acute conditions such as dehydration, serious infections, or acute myocardial infarction. Patients with acute and unstable heart failure, those scheduled for tests using iodinated contrast agents, and patients with hypersensitivity to this drug or biguanide drugs should also avoid using it. Patients with type 1 diabetes or metabolic acidosis, severe infections, or trauma with systemic disorders should temporarily discontinue treatment, and administration should be paused for some time before and after surgery. Patients with liver dysfunction, excessive alcohol consumption, dehydration, gastrointestinal disturbances such as diarrhea or vomiting should avoid using this drug. The use of this drug is also not recommended for patients during pregnancy with placental insufficiency, preeclampsia, or risk of intrauterine growth retardation. Patients with lactose intolerance or genetic metabolic abnormalities should not take this drug. Caution should be exercised when there are irregular meals or insufficient food intake, vigorous exercise, or interactions with other drugs, as there is a risk of lactic acidosis and hypoglycemia. Gastrointestinal symptoms such as diarrhea, nausea, and vomiting are common but mostly temporary. Serious side effects such as lactic acidosis, anemia, blood cell reduction, liver dysfunction, hypoglycemia may occur rarely, so if symptoms appear, immediate consultation with a healthcare professional is required. Regularly monitor kidney function to prevent the accumulation of this drug and the risk of lactic acidosis, especially in elderly patients or those with reduced kidney function. Alcohol can affect the metabolism of this drug and increase the risk of lactic acidosis, so excessive drinking should be avoided during use. Continuously monitor blood sugar control and take appropriate measures if hypoglycemic symptoms occur. When used in conjunction with other hypoglycemic agents, the hypoglycemic effect can be enhanced or reduced, so it is essential to consult with a healthcare professional regarding concomitant medications. Blood sugar control is crucial during pregnancy, and since this drug crosses the placenta, patients planning to become pregnant or those who are pregnant should determine whether to take this drug after consulting with a healthcare professional. If breastfeeding, since this drug is excreted in breast milk, it is advisable to discuss whether to continue breastfeeding or discontinue medication with a healthcare professional. Elderly individuals commonly have reduced kidney function, so dose adjustment and monitoring of kidney function are essential. In cases of overdose, there is a risk of lactic acidosis, so if suspected, immediate medical attention should be sought for appropriate treatment such as blood dialysis. This drug aids in blood sugar control without causing weight gain, but caution is needed when used in children or adolescents. Finally, keep this drug in a safe place out of the reach of children and avoid transferring it to other containers.

Side effects and when to seek care immediately

Serious side effects

  • Lactic acidosis
  • severe lactic acidosis
  • hypoglycemia
  • severe allergic reactions
  • severe skin reactions
  • liver impairment (jaundice)
  • severe edema or urinary abnormalities

Mild side effects

  • Diarrhea
  • nausea
  • vomiting
  • abdominal bloating
  • loss of appetite
  • indigestion
  • constipation
  • abdominal pain
  • metallic taste
  • rash
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  • anemia
  • leukopenia
  • thrombocytopenia
  • vitamin B12 deficiency
  • liver dysfunction
  • hypoglycemia

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

Storage

This drug should be stored in a tightly sealed container that is not exposed to air, and it is recommended to store it at room temperature between 1 and 30 degrees Celsius. This storage condition helps maintain the drug's efficacy for a longer period.

Appearance and packaging

Appearance

White, round film-coated tablet

Package unit

300 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.