Increase the sensitivity of peripheral tissues to insulin and increase insulin-mediated glucose utilization; increase the utilization of glucose by non-insulin-dependent tissues; inhibit hepatic gluconeogenesis and reduce hepatic glucose output; inhibit the uptake of glucose by intestinal wall cells; inhibit the biosynthesis and storage of cholesterol and reduce blood triglyceride and total cholesterol levels.

It can reduce fasting and postprandial hyperglycemia in patients with type 2 diabetes. Unlike insulin, it does not promote fat synthesis and has no obvious blood sugar lowering effect on normal people. It generally does not cause hypoglycemia when used alone in patients with type 2 diabetes.

Amlodipine is a calcium blocker (also known as a slow channel blocker or calcium ion antagonist) that blocks calcium ions from crossing the membrane into myocardial and vascular smooth muscle cells.

Calcium blockers (also known as slow channel blockers or calcium antagonists) block the entry of calcium ions across the membrane into myocardial and vascular smooth muscle cells.

Extract from the above information

This product is an oral selective histamine H1 receptor antagonist. It has no obvious anticholinergic and anti-5-hydroxytryptamine effects, and has a small central nervous system inhibitory effect.

This product is an oral selective histamine H1 receptor antagonist. It has no obvious anticholinergic and anti-5-hydroxytryptamine effects, and has a small central nervous system inhibitory effect.