Viewing nowGlimide 2mg Tablet (Glimepiride)
Glimepiride 2mg
Tablet · Prescription medication
Kuju Pharmaceutical Co., Ltd.

MFDS item code 201403417 · Approved 2014.07.25 · Insurance code 669804400
Improvement of blood sugar control in type 2 diabetes
This medication is used alongside dietary control and exercise therapy to assist in the blood sugar control of patients with type 2 diabetes. It can be used alone or in conjunction with insulin or other oral hypoglycemic agents if blood sugar control is insufficient. Particularly, when the effect of monotherapy with sulfonylureas or metformin is inadequate, it is administered together with metformin to improve blood sugar control. This medication effectively assists in improving blood sugar control in patients.
This medication is taken orally once a day. It should be taken before breakfast or just before the first meal. Start with an initial dose of 1 mg of glimepiride once a day. If necessary, the dose can be increased by 1 mg at 1 to 2-week intervals. Generally, once a dose exceeds 4 mg, additional effects are minimal; however, some patients may increase to 6 mg or 8 mg. Usually, a 4 mg dose per day is prescribed.
This medication should not be used in patients with insulin-dependent diabetes, diabetic ketoacidosis, or those in a coma. Additionally, patients who are allergic to this medication, sulfonylureas, or sulfonamides should not be administered this medication. There is no experience using this medication in patients with severe liver or kidney dysfunction, so transitioning to insulin therapy is recommended. This medication should also not be administered to pregnant women or those who may become pregnant, nor to breastfeeding women. Care must be taken in patients with severe infections, before and after surgery, or severe trauma, as insulin therapy may be required in these cases. Patients with gastrointestinal disorders, such as diarrhea or vomiting, may have impaired food absorption, increasing the risk of hypoglycemia. This medication contains lactose, so patients with lactose intolerance or specific genetic metabolic disorders should avoid taking it. During the first week of administration, the risk of hypoglycemia is high, so it is crucial to closely monitor blood sugar status. Elderly patients, those with poor nutritional status or irregular eating habits, and patients with an imbalance of exercise and carbohydrate intake should be particularly cautious if there is a change in eating patterns. Patients who frequently consume alcohol or have weakened liver or kidney function may also be at increased risk of hypoglycemia. Patients who overdose on this medication or have certain endocrine disorders, as well as those taking other medications simultaneously, must be cautious about blood sugar fluctuations. This medication can cause hypoglycemia, with symptoms such as headache, severe hunger, nausea, fatigue, anxiety, confusion, drowsiness, and decreased consciousness. Hypoglycemia can be quickly controlled by consuming sugar, so patients should always carry glucose with them. Additionally, gastrointestinal symptoms such as blurred vision, nausea, vomiting, and abdominal pain may also occur, and rare occurrences of liver dysfunction or blood abnormalities, as well as allergic reactions, can arise. If severe allergic reactions occur, medical attention should be sought immediately. This medication requires regular administration along with dietary management, exercise therapy, and, if necessary, weight management for optimal blood sugar control. It is important to adequately educate patients and their families about the symptoms and risks of hypoglycemia, as well as how to respond appropriately when it occurs. During stressful situations, such as trauma, surgery, or infections, blood sugar control may become challenging, thus temporarily transitioning to insulin therapy may be warranted. This medication is metabolized and excreted through the liver and kidneys, so dose adjustments may be needed for elderly patients with decreased renal or hepatic function. If taken with other medications, it can affect blood sugar control, so all medications being taken should be disclosed to a physician or pharmacist. Care should particularly be taken regarding interactions with beta-blockers, antibiotics, and steroids. In the case of overdose, severe hypoglycemia may occur, so immediate medical attention is required, including emergency measures such as inducing vomiting, administering activated charcoal, or glucose injection. Finally, the safety and efficacy of this medication in children have not been established, and it should not be used by pregnant or breastfeeding women. Medications should be stored out of the reach of children and kept in their original containers for safety.
Not everyone experiences these, and they can vary from person to person.
This medication is sensitive to air and moisture, so it must be stored in a tightly sealed container. It is important to maintain storage temperatures between 1 degree and 30 degrees Celsius.
Green oblong tablet
30 tablets/bottle, 300 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.