Medication info

Lotra Tablets (Glimipiride)

Prescription medicationTablet경구Approval withdrawn
Ingredient · strength
Glimepiride›2mg / 1 tablet
Manufacturer / importer
에스케이케미칼(주)
Appearance
Green rectangular tablet
Packaging
30 tablets/bottle, 200 tablets/bottle
Approval status
Approval withdrawn

MFDS item code 200402453 · Notified 2004.02.06 · Insurance code 644700410

This product's status changed to Approval withdrawn on 2025.12.03. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Improves blood sugar control in type 2 diabetes
Who takes it
Adults
Adult dose
Individually adjusted for each patient. Swallow without chewing with more than 1/2 cup of water. Administer 1 time a day orally. It should be taken before breakfast or immediately before the first meal. Initial dosage for monotherapy: Start with a daily dose of 1 mg of Glimepiride, increasing by 1 mg at 1- to 2-week intervals, generally, doses exceeding 4 mg offer minimal additional effect, but a maximum of 6 mg may be considered.

Ingredients

Manufacturer
에스케이케미칼(주)

Efficacy & effects

Improves blood sugar control in type 2 diabetes

View approved original text

This medication is used to improve blood sugar control in patients with type 2 diabetes in conjunction with dietary and exercise regimens. It can be administered alone and is also effective when used in combination with oral hypoglycemic agents or insulin in cases where blood sugar control is difficult. Particularly in cases where sulfonylureas or metformin therapy is insufficient, it is used in combination with metformin to enhance blood sugar control. This medication plays a crucial role in comprehensive blood sugar management and diabetes treatment.

How to take

Adult dose

Individually adjusted for each patient. Swallow without chewing with more than 1/2 cup of water. Administer 1 time a day orally. It should be taken before breakfast or immediately before the first meal. Initial dosage for monotherapy: Start with a daily dose of 1 mg of Glimepiride, increasing by 1 mg at 1- to 2-week intervals, generally, doses exceeding 4 mg offer minimal additional effect, but a maximum of 6 mg may be considered.

Precautions

This medication should not be used in patients with insulin-dependent diabetes or those in diabetic ketoacidosis or coma. Patients who have had allergic reactions to this medication or its components, as well as others in the same class, should avoid use. It is recommended to switch to insulin treatment for patients with severely impaired liver or kidney function. It is also advisable for women who are pregnant or may become pregnant, as well as nursing mothers, to avoid using this medication. Insulin treatment may be more appropriate for patients with severe infections, perioperative status, or significant trauma. Caution is advised if gastrointestinal disturbances may hinder food absorption, increasing the risk of hypoglycemia. During the first week of starting this medication, the risk of hypoglycemia is heightened, and blood sugar levels should be closely monitored. Particular precautions should be taken for the elderly, individuals with poor nutritional status or irregular eating habits, imbalances in exercise and diet, changes in eating patterns, and frequent alcohol consumption. Patients with compromised kidney or liver function may also respond more sensitively to this medication, necessitating dose adjustments. Furthermore, those with other endocrine disorders or taking multiple medications should consult a doctor, as the risk of hypoglycemia may increase. When using this medication, one should be aware of possible hypoglycemic symptoms such as headaches, severe hunger, nausea, fatigue, confusion, dizziness, drowsiness, and decreased consciousness. It is critical to consume carbohydrate-containing foods immediately if hypoglycemic symptoms occur. Some patients may experience temporary blurred vision or gastrointestinal symptoms, as well as abnormalities in liver function, blood changes, or allergic reactions. Serious allergic reactions such as urticaria or difficulty breathing require immediate medical attention. This medication must be used alongside dietary and exercise regimens for blood sugar control and should be taken regularly. To prevent hypoglycemic symptoms, it is advised to always carry carbohydrates and ensure that family members are aware of hypoglycemia symptoms and treatment methods. In stressful situations or after surgery or infections where blood sugar control becomes challenging, transitioning to insulin therapy may be necessary. This medication can interact with other medications, so it is essential to inform your doctor or pharmacist of any other drugs being taken. Particularly, changes in blood sugar levels may occur when taken with certain antibiotics, antifungals, antihypertensives, anticoagulants, and beta-blockers. It is safest for pregnant or nursing women to avoid this medication, and insulin treatment should be considered if necessary. In cases of overdose, severe hypoglycemia can occur, necessitating immediate medical assistance and observation in a hospital until blood sugar levels are fully restored. This medication should be kept out of the reach of children, stored in its original container, and taken precisely as directed by a physician.

Side effects and when to seek care immediately

Serious side effects

  • Urticaria
  • severe swelling (edema)
  • chest tightness
  • difficulty breathing
  • cold sweat
  • pallor
  • severe rash with fever
  • blisters
  • peeling skin
  • pain in mucous membranes of mouth/eyes
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  • jaundice of skin or eyes
  • extreme lethargy
  • sudden and severe headache
  • thunderclap headache
  • seizures
  • confusion of consciousness
  • visual disturbances
  • paralysis
  • significantly decreased urine output
  • extensive systemic edema
  • increased blood pressure
  • thrombocytopenia
  • leukopenia
  • hemolytic anemia.

Mild side effects

  • Headache
  • severe hunger
  • nausea
  • vomiting
  • fatigue
  • sleep disturbances
  • anxiety
  • aggression
  • decreased concentration
  • decreased agility or motivation
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  • depression
  • confusion
  • speech disturbances
  • aphasia
  • visual disturbances
  • tremors
  • incomplete paralysis
  • sensory disturbances
  • dizziness
  • weakness
  • loss of self-control
  • temporary mental confusion
  • drowsiness
  • shallow breathing
  • bradycardia
  • sweating
  • cold and damp skin
  • tachycardia
  • hypertension
  • palpitations
  • angina
  • deep vein thrombosis
  • blurred vision
  • abdominal discomfort.

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

Storage

This medication must be stored in a tightly sealed container to avoid exposure to air or moisture. It is best to store it at room temperature, ideally between 1 and 30 degrees Celsius.

Appearance and packaging

Appearance

Green rectangular tablet

Package unit

30 tablets/bottle, 200 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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For anything that needs medical judgment, consult a doctor or pharmacist.

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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.