Anti-Diabetic/OHA
 
  TeneBest


Each film coated tablet contains :

Teneligliptin 20 mg


About the drug : Teneligliptin belongs to a class of drugs called DPP-4 Inhibitors.

Teneligliptin has a “J” shaped or anchor hooked domain structure because of which it has more potent inhibition of DPP-4 enzyme as compared to Sitagliptin & Vildagliptin. Teneligliptin significantly controls Glycaemic parameters with safety & no dosages adjustment is required even in renallyimpared patients.

 
  Voglisis .2 & .3


Each film coated tablet contains :

Voglibose .2
Voglibose .3

About the drug :Voglisis is a Alpha-glucosidase inhibitors.

Alpha-glucosidase inhibitors are oral anti-diabetic drugs used for diabetes mellitus type 2 that work by preventing the digestion of carbohydrates (such as starch and table sugar).

Voglibose delays the absorption as well as digestion of dietary polysaccharides by reversibly inhibiting carbohydrate digestive enzymes like sucrose, maltose etc. This results in a reduction in PPHG. Voglibose has no inhibitory activity against lactase and so, it does not cause lactose intolerance and diarrhea.

 
  Glynova


Glynova-2

Each uncoated tablet contains :

Glimepiride 2 mg

Glynova-4

Each uncoated tablet contains :

Glimepiride 4 mg


About the Drug : Glimepiride is a medium- to long-acting sulfonylurea Antidiabetic drug. Glimepiride is indicated to treat type 2 diabetes mellitus; its mode of action is to increase insulin production by the pancreas.


Glynova-M1

Each uncoated bilayered tablet contains :

Glimepiride 1 mg


Metformin HCl 500 mg


(In sustained release form)



Glynova-M2

Each uncoated bilayered tablet contains :

Glimepiride 2 mg


Metformin HCl 500 mg


(In sustained release form)


About the Drug : This is an ideal combination for Type 2 DM as Glimepiride stimulates the insulin release from functioning pancreatic β-cells and inhibits gluconeogenesis at hepatic cells & also increases insulin sensitivity at peripheral target sites whereas Metformin decreases hepatic gluconeogenesis, decreases intestinal absorption of glucose and improves insulin sensitivity (increases peripheral glucose uptake and utilisation).


Glynova-MP1

Each uncoated bilayered tablet contains :

Pioglitazone Hydochloride 15 mg


Metformin HCl 500 mg


(In sustained release form)


Glimepiride 1 mg


Glynova-MP2

Each uncoated bilayered tablet contains :

Pioglitazone Hydochloride 15 mg


Metformin HCl 500 mg


(In sustained release form)


Glimepiride 2 mg


About the Drug : The combination of Glimepiride, Pioglitazone and Metformin sustained-release complements each other and provides better glycemic control in the management of Type-2 diabetes and probably in the prevention of its associated macrovascular and microvascular complications.

Glimepiride lowers blood glucose by stimulating the release of insulin from functioning pancreatic beta cells.

Pioglitazone selectively stimulates the nuclear receptor peroxisome proliferator activated receptor gamma (PPAR-γ) and to a lesser extent PPAR-GAMMA. It modulates the transcription of the insulin-sensitive genes involved in the control of glucose and lipid metabolism in the muscle, adipose tissue and the liver. As a result pioglitazone reduces insulin resistance in the liver and peripheral tissues; increases the expense of insulin-dependent glucose; decreases withdrawal of glucose from the liver; reduces quantity of glucose, insulin and glycated haemoglobin in the bloodstream. Metformin decreases hepatic glucose production, decreases intestinal absorption of glucose, and improves insulin sensitivity by increasing peripheral glucose uptake and utilization.

 
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