TOLBUTAMIDE
It is classified as first generation sulfonylurea, sole significant action being lowering of blood glucose level in normal and non-insulin dependent diabetics, but not in insulin depedent diabetics. Its mechanism of action is like Glibenclamide.Non-insulin dependent diabetes mellitus (Type II, maturity onset diabetes) whenever dietary treatment alone proves inadequate.
1.0 gm a single daily dose before breakfast or the first substantial meal. If more than 1.0 gm daily is required, the rest can be taken before the evening meal. Max : 0.5-2 gm. daily.
Insulin dependent diabetes mellitus (Type 1, juvenile diabetes). diabetic coma diabetic metabolic decompensation (ketoacidosis), severe impairment of renal function, hypersensitivity.
Compliance to diet and regular medication are of utmost importance for success of treatment. Altered alertness and capacity to react may be impaired. Driving vehicle or to operate machinery. Alcohol might attenuate or potentiate effect of tolbutamide. Paediatrics: Should not be used. Pregnancy & Lactation: Should not be used. Elderly: Safe.
Nausea, sensation of gastric fullness, transient changes of haemotopoietic system. Hypersensitivity skin reactions.
Hypoglycaemic effect enhanced by dicoumarol, clofibrate, chloramphenicol & cyclophosphamide & effect reduced by corticosteroids, adrenaline, oral contraceptives & thiazide diuretics.
Brand Name | Manufactured by |
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Rastinon | SANOFI AVENTIS PHARMA LTD. |
Told | LOTUS PHARMACEUTICALS |