Medication info

Dibet Tablet (Bogligibose)

Prescription medicationApproval withdrawn
Ingredient · strength
Voglibose›Strength being verified
Manufacturer / importer
Daehwa Pharmaceutical Co., Ltd.
Appearance
White to light yellow round tablet
Packaging
Domestic use - 30 tablets/bottle, Domestic use - 300 tablets/bottle, Export use - 90 tablets/box [(10 tablets/blister x 9)]
Approval status
Approval withdrawn

MFDS item code 200503335 · Approved 2005.11.01

This product's status changed to Approval withdrawn on 2023.06.08. It may no longer be sold, so consult a doctor or pharmacist before taking it.

Summary

Main use
Improvement of postprandial hyperglycemia in diabetes mellitus
Who uses it
Adults
Adult dosage
The response and tolerability vary among patients, so the physician must determine the dose according to the patient's condition. The usual dosage is as follows. Adults are generally administered voglibose 0.2mg per dose orally 3 times daily before each meal. If the effect is insufficient, the dose per administration may be increased to 0.3mg while carefully monitoring the patient's progress.

Ingredients

Manufacturer
Daehwa Pharmaceutical Co., Ltd.

Efficacy & effects

Improvement of postprandial hyperglycemia in diabetes mellitus

  • Diabetes
  • postprandial hyperglycemia
View approved original text

This medication is used for patients with diabetes who have difficulty controlling post-meal blood sugar levels despite following dietary and exercise regimens. It is also administered as an additional treatment for patients who are already on oral hypoglycemics or insulin therapy when blood sugar improvement is insufficient, effectively managing postprandial hyperglycemia. This helps to stabilize blood sugar levels and aids in the prevention of complications related to diabetes.

Dosage and Administration

Adult dosage

The response and tolerability vary among patients, so the physician must determine the dose according to the patient's condition. The usual dosage is as follows. Adults are generally administered voglibose 0.2mg per dose orally 3 times daily before each meal. If the effect is insufficient, the dose per administration may be increased to 0.3mg while carefully monitoring the patient's progress.

Precautions

This medication should not be used in patients with severe conditions such as severe ketoacidosis or diabetic coma. It is also advisable not to administer this drug to patients with severe infections or those undergoing surgery, or to patients who have sustained severe trauma. Patients with allergies to any component of this medication should avoid using it. This medication contains lactose; therefore, it should not be administered to patients with lactose intolerance or galactose metabolism disorders. Patients with gastrointestinal issues or chronic intestinal diseases should use this medication cautiously as symptoms may worsen. Patients experiencing increased intestinal gas may need to be monitored closely, particularly those with a history of abdominal surgery or conditions like bowel obstruction or colonic stricture. Caution is required when administering this drug to patients with severely impaired liver or kidney function as drug metabolism may be affected. Older adults may have reduced bodily functions; therefore, treatment should start at a lower dose, with careful monitoring of their condition. When used in conjunction with other hypoglycemic agents, there is a risk of hypoglycemia; hence, treatment should begin at a lower dose while closely observing symptoms. If hypoglycemic symptoms occur during use, administering glucose instead of sugar is effective; in severe cases, proper treatment should be sought in a medical facility. Symptoms such as abdominal distension, increased flatulence, and, rarely, bowel obstruction may occur; drug use should be discontinued immediately if symptoms worsen. If symptoms of liver dysfunction or jaundice arise, use should be stopped immediately and consultation with healthcare providers is necessary. In patients with liver cirrhosis, constipation can lead to elevated ammonia levels and altered mental status, so bowel habits should be monitored carefully. Gastrointestinal symptoms such as diarrhea, abdominal pain, nausea, and vomiting may occur, as well as allergic reactions such as skin rash or itching. Neurological symptoms, including headaches, dizziness, and drowsiness, can occur; hence caution is needed when driving or operating machinery. Blood abnormalities such as anemia or thrombocytopenia have also been reported, so any unusual symptoms should be reported to healthcare providers. Women who are pregnant or may become pregnant should only use this medication if absolutely necessary due to uncertain safety. It is advisable for breastfeeding women to avoid using this medication if possible. The safety of this medication in pediatric patients has not been established, so its use is not recommended. Older adults may have declining physiological functions, hence treatment should begin at a lower dose, with careful monitoring of blood sugar and gastrointestinal symptoms. Regular blood sugar checks and monitoring of therapeutic effects and side effects should be conducted during the use of this medication. Additionally, patients should inform healthcare providers of any other medications they are taking that may affect blood sugar control.

Side effects

  • Hypoglycemia
  • abdominal distension
  • increased flatulence
  • intestinal obstruction
  • acute hepatitis
  • increased AST
  • increased ALT
  • severe hepatic impairment
  • jaundice
  • worsening hyperammonemia
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  • altered consciousness
  • diarrhea
  • loose stools
  • abdominal cramping
  • abdominal pain
  • constipation
  • loss of appetite
  • nausea
  • vomiting
  • heartburn
  • indigestion
  • stomatitis
  • thirst
  • taste disturbance
  • intestinal cystic pneumatosis
  • feeling of incomplete bowel movement
  • gastritis
  • rash
  • itching
  • photosensitivity
  • increased AST
  • increased ALT
  • increased LDH
  • increased γ-GTP
  • increased ALP
  • headache
  • dizziness
  • unsteadiness
  • drowsiness
  • anemia
  • thrombocytopenia
  • tingling
  • facial swelling
  • blurred vision
  • flushing
  • lethargy
  • weakness
  • hyperkalemia
  • increased serum amylase
  • decreased HDL cholesterol
  • sweating
  • hair loss
  • glossitis

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

Storage

This medication should be stored in a tightly sealed container to prevent exposure to air, preferably at room temperature between 1 and 30 degrees Celsius. Proper storage can help maintain the medication's effectiveness and prevent deterioration.

Appearance and packaging

Appearance

White to light yellow round tablet

Package unit

Domestic use - 30 tablets/bottle, Domestic use - 300 tablets/bottle, Export use - 90 tablets/box [(10 tablets/blister x 9)]

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.