Our combination contains voglibose and metformin is an alpha-glucosidase inhibitor used for lowering post-prandial blood glucose levels in people with diabetes mellitus. Voglibose delays the absorption of glucose thereby reduces the risk of macrovascular complications.
Metformin is an oral antidiabetic drug in the biguanide class. It is the first-line drug of choice for the treatment of type 2 diabetes, in particular, in overweight and obese people and those with normal kidney function.
For the treatment of diabetes. It is specifically used for lowering post-prandial blood glucose levels thereby reducing the risk of macrovascular complications.
Rationale of Combination:
âMetformin is the only antidiabetic drug that has been conclusively shown to prevent the cardiovascular complications of diabetes. It helps reduce LDL cholesterol and triglyceride levels, and is not associated with weight gain.
âIt is also used in the treatment of polycystic ovary syndrome, and has been investigated for other diseases where insulin resistance may be an important factor.
When voglibose is used in combination with derivative(s) of sulfonylamide, sulfonylurea or biguanide, or with insulin, hypoglycemic symptoms may occur. Therefore, when used in combination with any of these drugs, care should be taken, such as starting the administration at a low dose.
When voglibose is administered concomitantly with drugs that enhance or diminish the hypoglycemic action of antidiabetic drugs, caution should be taken as this might additionally delay the action of voglibose on the absorption of carbohydrates. Examples of drugs enhancing the hypoglycemic action of antidiabetic drugs: Î²blockers, salicylic acid preparations, monoamine oxidase inhibitors and fibrate derivatives. Examples of drugs diminishing the hypoglycemic action of antidiabetic drugs: epinephrine, adrenocortical hormone, and thyroid hormone.
The following medicines may interact with Metformin hydrochloride:
âiodinated contrast media
âother oral antidiabetics
Mechanism of Action:
Voglibose is an alpha-glucosidase inhibitor which reduces intestinal absorption of starch, dextrin, and disaccharides by inhibiting the action of Î±-glucosidase in the intestinal brush border. Inhibition of this enzyme halts the decomposition of disaccharides into monosaccharides and slows the digestion and absorption of carbohydrates; the postprandial rise in plasma glucose is blunted in both normal and diabetic subjects resulting in improvement of post-prandial hyperglycemia and various disorders caused by hyperglycemia. Î±-glucosidase inhibitors do not stimulate insulin release and therefore do not result in hypoglycemia.
Metformin is a biguanide with antihyperglycemic effects, lowering both basal and postprandial plasma glucose. It does not stimulate insulin secretion and therefore does not produce hypoglycemia. Metformin may act via 3 mechanisms:
âBy reducing hepatic glucose production through inhibition of gluconeogenesis and glycogenolysis.
âBy increasing insulin sensitivity in muscle, improving peripheral glucose uptake and utilization.
âBy delaying intestinal glucose absorption.
Absorption: Voglibose is poorly absorbed after oral dosing. Plasma concentrations after oral doses have usually been undetectable.
Distribution: After ingestion of voglibose (and other glucosidase inhibitors), the majority of active unchanged drug remains in the lumen of the gastrointestinal tract to exert its pharmacological activity.
Metabolism: Voglibose is metabolized by intestinal enzymes and by the microbial flora.
Elimination: Voglibose is excreted in the urine and feces.
Absorption: After an oral dose of metformin, time to peak plasma concentration (Tmax) is reached in 2.5 hours. Absolute bioavailability of a 500 mg metformin tablet is approximately 50% to 60% in healthy subjects. Food decreases the extent of absorption and slightly delays absorption.
Distribution: Plasma protein binding is negligible. Metformin partitions into erythrocytes. The blood peak is lower than the plasma peak and appears approximately the same time. The red blood cells most likely represent a secondary compartment of distribution. The mean Vd ranges between 63 to 276 L.
Metabolism: Metformin is excreted unchanged in urine. No metabolites have been identified in humans.
Elimination: Renal clearance of metformin is >400 ml/min, indicating that metformin is eliminated by glomerular filtration and tubular secretion. Following an oral dose, the apparent terminal elimination half-life is approximately 6.5 hours. When renal function is impaired, renal clearance is decreased in proportion to that of creatinine and thus the elimination half-life is prolonged, leading to increased levels of metformin in plasma.
Common Side Effects:
Gastrointestinal disorders such as, abdominal pain, constipation, anorexia, nausea, vomiting, diarrhea, and loss of appetite.
â Hypersensitivity to metformin, voglibose, or to any of the excipients
âDiabetic ketoacidosis, diabetic pre-coma
âSevere infection, before and after operation or with serious trauma
âGastrointestinal obstruction or predisposed to it
âRenal failure or renal dysfunction (creatinine clearance Ë 60 ml/min)
âAcute conditions with the potential to alter renal function such as:
intravascular administration of iodinated contrast agents
âAcute or chronic disease which may cause tissue hypoxia such as:
cardiac or respiratory failure
recent myocardial infarction
Hepatic insufficiency, acute alcohol intoxication, alcoholism
In Pregnancy and Lactation: To date, no relevant epidemiological data are available. Animal studies do not indicate harmful effects with respect to pregnancy, embryonal or fetal development, parturition or post natal development, therefore the drug should be given to pregnant women or women suspected of being pregnant only when the potential benefits outweigh the possible hazards.
Store in a cool, dry place.
Protect from light.
Keep the medicine out of reach of children.