Viewing nowMetformin Tablets 500mg (Metformin Hydrochloride)
Metformin Hydrochloride 500mg
Tablet · Prescription medication
KMS Pharmaceutical Co., Ltd.

MFDS item code 201500640 · Approved 2015.02.06 · Insurance code 654701580
Improvement of Type 2 Diabetes (blood sugar control)
This medication is used for the treatment of patients with Type 2 diabetes whose blood sugar control is not adequately managed with diet and exercise alone. It is particularly effective in overweight adult diabetic patients and can be used alone or in combination with other oral hypoglycemic agents or insulin. Additionally, it can also be used as monotherapy or in combination with insulin in children over the age of 10 and adolescents. This helps improve blood sugar control and maintain health.
The dosage must be determined individually based on the drug's efficacy and tolerance, and should not exceed the recommended maximum daily dose. This medication should always be started at a low dose to reduce gastrointestinal side effects and to determine the minimum effective dose for proper blood sugar control, and should be taken 500mg during meals 2-3 times a day. The dosage should be gradually increased by 500mg each week, reaching a total of 20
Children over 10 years or adolescents are administered 500mg once daily during or after meals. Blood sugar levels should be measured after one week to adjust the dosage, and gastrointestinal side effects may gradually improve.
This medication may cause serious side effects such as severe lactic acidosis or hypoglycemia, so caution is needed. It should not be given to patients with moderate to severe renal impairment or those in acute conditions such as dehydration, severe infections, or acute myocardial infarction. In patients with acute and unstable heart failure, as well as before and after examinations using iodine contrast agents, this medication should be discontinued, and re-administration can only occur after kidney function has recovered to normal. It is not to be used in patients who have had allergic reactions to this medication or similar drugs, in type 1 diabetes patients, or in patients with a history of lactic acidosis or diabetic ketoacidosis. It should be used with caution in patients with severe infections, severe trauma, pre- and post-surgery, malnutrition, or liver or lung dysfunction, and administration should be temporarily stopped if necessary. This medication contains lactose, so it should not be given to patients with lactose intolerance or related genetic conditions. Caution is also required in cases of irregular meals, excessive exercise, or interactions with other medications, which may increase the risk of hypoglycemia or lactic acidosis. Lactic acidosis, though rare, can be fatal, so any symptoms such as malaise, muscle pain, shortness of breath, or abdominal pain should be immediately reported to medical personnel. Gastrointestinal disturbances are common at the initiation of treatment but are usually temporary and can be alleviated by taking the medication with meals or gradually increasing the dosage. Blood sugar control status should be regularly monitored, and kidney function and hematological values should be consistently monitored. Alcohol may increase the risk of side effects from this medication, so excessive drinking should be avoided. During pregnancy, it may affect the fetus, so it is essential to consult a physician if planning to become pregnant or during pregnancy, and it should not be administered if there is a risk of placental insufficiency or preeclampsia. During breastfeeding, as this medication may be secreted in breast milk, careful consideration should be given to whether to continue nursing or stop medication. In elderly patients, kidney function may decline, so dose adjustment and regular kidney function tests are necessary, and it is advisable not to administer the maximum dosage. In cases of overdose, the drug can be removed through hemodialysis, so if overdose occurs, medical attention should be sought immediately. This medication may interact with other hypoglycemic agents or multiple medications, so it is essential to inform medical personnel of any concurrent medications and closely monitor blood sugar and the patient's condition. Finally, this medication should be kept out of reach of children, and care should be taken not to transfer it to other containers as this may affect its quality.
Lactic acidosis, severe allergic reactions (rash), hypoglycemia, liver abnormalities (possible liver function impairment)
Gastrointestinal symptoms (diarrhea, nausea, vomiting, abdominal bloating, loss of appetite, indigestion, constipation, abdominal pain), metallic taste, anemia, leukopenia, thrombocytopenia, vitamin B12 deficiency, liver function abnormalities, severe delayed hypoglycemia
Not everyone experiences these, and they can vary from person to person.
This medication may be sensitive to air or moisture, so it must be stored in a tightly sealed container. Additionally, it is important to store it at room temperature, specifically between 1 degree and 30 degrees Celsius, to maintain its effectiveness.
White round film-coated tablets
30 tablets/bottle, 500 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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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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For anything that needs medical judgment, consult a doctor or pharmacist.
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.