Medication info
Dabist Tablet (Metformin Hydrochloride)

Dabist Tablet (Metformin Hydrochloride)

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

MFDS item code 202002163 · Approved 2020.03.27 · Insurance code 648508010

Summary

Main use
Improvement of type 2 diabetes (blood sugar control)
Who uses it
Adults · Children
Adult dosage
The dosage should be determined based on individual drug efficacy and tolerance, without exceeding the recommended maximum daily dose. This medication should be started at a low dose to minimize gastrointestinal adverse reactions while confirming the minimum effective dose needed for adequate blood sugar control, administered 2-3 times daily, with 500 mg taken with meals. Doses can be gradually increased by 500 mg weekly until reaching 20
Children's dosage
This medication can be used in children over 10 years old or adolescents during growth. The general initial dosage is 500 mg once daily, administered during or after meals. After one week, measure blood sugar levels

Ingredients

Manufacturer
신풍제약(주)

Efficacy & effects

Improvement of type 2 diabetes (blood sugar control)

  • Patients with type 2 diabetes
  • overweight diabetes patients
View approved original text

This medication is used for the treatment of type 2 diabetes patients who have difficulty controlling blood sugar with diet and exercise alone. It can be used alone or in combination with other oral hypoglycemics or insulin, particularly in overweight adult patients. It also helps in blood sugar control in children over 10 years old and adolescents during growth, either as monotherapy or in combination with insulin. This medication is effectively used across various age groups to control blood sugar in diabetes treatment.

Dosage and Administration

Adult dosage

The dosage should be determined based on individual drug efficacy and tolerance, without exceeding the recommended maximum daily dose. This medication should be started at a low dose to minimize gastrointestinal adverse reactions while confirming the minimum effective dose needed for adequate blood sugar control, administered 2-3 times daily, with 500 mg taken with meals. Doses can be gradually increased by 500 mg weekly until reaching 20

Children's dosage

This medication can be used in children over 10 years old or adolescents during growth. The general initial dosage is 500 mg once daily, administered during or after meals. After one week, measure blood sugar levels

Precautions

This medication may cause severe lactic acidosis or hypoglycemia, requiring caution. It should not be administered to patients with moderate to severe renal impairment or acute conditions such as dehydration, severe infections, cardiovascular collapse, acute myocardial infarction, or sepsis. Patients with acute heart failure or those receiving intravenous radiographic iodine contrast agents should also not use this medication, and administration should be paused for a certain period before and after contrast testing. Use is prohibited for patients with allergic reactions to this medication or biguanide drugs, or a history of type 1 diabetes, lactic acidosis, or diabetic ketoacidosis. In patients with severe infections, serious traumatic systemic disorders, pre- and post-surgery, malnutrition, liver dysfunction, pulmonary embolism, or severe pulmonary dysfunction, administration should be temporarily halted or avoided. Caution is required in patients with irregular meals, inadequate food intake, vigorous exercise, or taking interacting drugs, as there is a risk of lactic acidosis and hypoglycemia. Lactic acidosis is very rare but can be fatal, so if symptoms occur, immediately discontinue use and consult healthcare professionals. Gastrointestinal symptoms such as diarrhea, nausea, and vomiting may commonly occur during initial treatment, but they usually disappear over time. This medication is primarily excreted through the kidneys; therefore, regular kidney function tests should be performed, and if renal function declines, discontinuation or dose adjustment may be necessary. Alcohol can affect the metabolism of this medication; excessive alcohol consumption should be avoided. Vitamin B12 deficiency may occur, so regular blood tests are recommended. During pregnancy, since it crosses the placenta, fetal growth monitoring is necessary, and use should be avoided in certain pregnancy conditions. If breastfeeding, this medication is excreted in breast milk, so careful consideration regarding the continuation of breastfeeding or treatment is required. Elderly patients may have a risk of decreased renal function, thus dose adjustment and regular monitoring of renal function are necessary. This medication may interact with various drugs; therefore, consultation with healthcare professionals regarding concomitant medications is advised. In cases of overdose, blood dialysis may be beneficial, so seek immediate medical attention. This medication does not cause weight gain, thus favorably assisting in weight management, and may help in blood sugar control and reduction of diabetes-related complications with long-term use. Store out of reach of children, and avoid transferring to another container.

Side effects and when to seek care immediately

Serious side effects

Lactic acidosis (acute renal function deterioration, metabolic complications associated with cardiopulmonary diseases, sepsis), severe allergic reactions (such as rash), serious neurological symptoms (severe headache, confusion), liver abnormalities (possible jaundice due to liver dysfunction), hypoglycemia (severe delayed hypoglycemia), significant edema and urinary abnormalities (severe swelling, decreased renal function), respiratory problems (if shortness of breath occurs)

Mild side effects

Gastrointestinal symptoms (diarrhea, nausea, vomiting, abdominal distension, loss of appetite, indigestion, constipation, abdominal pain), unpleasant or metallic taste, rash, anemia, leukopenia, thrombocytopenia, vitamin B12 deficiency, abnormal liver function, hypoglycemia, failure to control blood sugar, etc.

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

Storage

This medication should be stored in a sealed container to prevent air or moisture ingress. It is recommended to keep the medication at room temperature, between 1°C and 30°C, not too hot or too cold.

Appearance and packaging

Appearance

White round film-coated tablets

Package unit

500 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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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.