GLUMIN Tablet
ក្រុមហ៊ុនផលិតឱសថ:
PT Dexa Media, Indonesia
ក្រុមហ៊ុនចែកចាយឱសថនៅប្រទេសកម្ពុជា:
Dynamic Pharma
- សារធាតុសកម្ម
- ប្រសិទ្ធិភាពព្យាបាល និង កម្រិតប្រើប្រាស់
- ហាមប្រើ
- ផលរំខាន
- អន្តរប្រតិកម្ម
- ស្ត្រីមានផ្ទៃពោះ និង ស្ត្រីបំបៅដោះកូន
- ការប្រុងប្រយ័ត្នជាពិសេស បរិយាយប័ណ្ណឱសថ
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សារធាតុសកម្ម
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ប្រសិទ្ធិភាពព្យាបាល និង កម្រិតប្រើប្រាស់
Treatment for newly diagnosed maturity-onsel patients with or without overweight problem and failure of dietetic therapy.
-As a combination therapy for diabetics unresponsive to single therapy of sulfonylurea either primary or secondary.
-Adjuvant therapy to lower insulin dosage if required.
GLUMIN® should be taken in divided doses with meals or after meals.
Dosage :
Tablet 500mg: 500 mg tablet, 3 times daily
Tablet 850mg: initial dose 850mg tablets, 1 time daily (morning), Maintenance dose: 850mg tablets, twice daily (morning and night)
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ហាមប្រើ
Patients with cardiac failure, renal dysfunction, impaired hepatic function, dehydration and alcoholism, diabetic coma, ketoacidosis, myocardial infarction, chronic or acute diseases states associated with tissue hypoxia, diseases states associated with lactic acidosis such as shock, pulmonary insufficiency, lactic acidosis history.
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ផលរំខាន
GLUMIN® causes reversible gastrointestinal tract side effects including anorexia, abdominal disturbances, nausea, vomiting, metalic taste and diarrhea.
Lactic acidosis can occur but death incidences 10-15 times less than phenformin and less than hypoglycemia case caused by glibenclamide/sulfonylurea.
Lactic acidosis can be treated with sodium bicarbonate.
Individual case with metformin are megaloblastic anemia, pneumonitas, vasculitis.
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អន្តរប្រតិកម្ម
Acarbose a-glucosidase inhibitor decreases bioavailability and average maximum concentration plasma of metformin but the onset time is not changed.
-Guar gum can decrease absorption rate of metformin and decrease blood concentration of metformin.
-Cimetidine inhibits renal tubular secretion metformin competitively and increases area under plasma concentration of metformin vs time curve and decreases renal excretion of metformin.
- Oral anticoagulant phenprocoumon increases elimination of this drugs, increases hepatic blood flow and hepatic extraction as metformin effect at microsomal enzyme activity.
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ស្ត្រីមានផ្ទៃពោះ និង ស្ត្រីបំបៅដោះកូន
Although embryonic side effects do not occur on administration metformin in diabetic pregnant women, insulin better than oral anti hyperglycemia agent for hyperglycemia controlled in pregnancy.
-Not recommended for use in nursing mothers.
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ការប្រុងប្រយ័ត្នជាពិសេស
- Stimulating conditions of hypoxia and lactic accumulation may cause seriously lactic acidosis, GLUMIN should not be used in patients with cardiovascular diseases, renal dysfunction, impaired hepatic function, dehydration and alcoholism.
- Long-term therapy of GLUMIN, can causes failure absorption of vitamin B12 and folic acid in the gastrointestinal tract. Therefore, serum B12 levels should be checked every year.
- Although embryonic side effects do not occur on administration metformin in diabetic pregnant women, insulin better than oral anti hyperglycemia agent for hyperglycemia controlled in pregnancy.
- Not recommended for use in nursing mothers.
- The possibly of interactions between metformin with certain anticoagulants, dosage of anticoagulant may adjustment.
- In patient of elderly, serious infection and trauma conditions should be used with caution.
*ព័ត៌មានឱសថត្រូវបានរៀបរៀងដោយ អ៊ីម៉ាតុគឹ មេឌីក (ខេមបូឌា) ដោយផ្អែកលើប្រភពព័ត៌មានខាងក្រោម។ សម្រាប់ព័ត៌មានលម្អិត សូមស្វែងរកនៅក្នុងក្រដាសព័ត៌មាននៃឱសថនីមួយៗ ឬ សាកសួរទៅកាន់ក្រុមហ៊ុនឱសថឬតំណាងចែកចាយនៃឱសថនីមួយៗ។
ប្រភពព័ត៌មាន៖
- ក្រដាសព័ត៌មាននៃឱសថសម្រាប់អ្នកជំនាញវេជ្ជសាស្ត្រដែលប្រើប្រាស់នៅប្រទេសជប៉ុន (Pharmaceutical and Medical Devices Agency, Pmda): https://www.pmda.go.jp
- ព័ត៌មានសង្ខេបនៃឱសថសម្រាប់អ្នកជំងឺដែលប្រើប្រាស់នៅប្រទេសជប៉ុន: http://www.rad-ar.or.jp