This product is an acidic polysaccharide drug with strong dispersing and emulsifying properties, improving the viscoelasticity of blood rheology; its anticoagulant effect is equivalent to 1/3 to 1/2 of heparin, and can prevent platelet adhesion to collagen and inhibit platelet aggregation; it has a significant effect on lowering blood lipids, and can reduce cholesterol, triglycerides, low-density lipoprotein and very low-density lipoprotein, while increasing high-density lipoprotein levels; it inhibits the occurrence and development of atherosclerotic lesions; it has the effects of dilating peripheral blood vessels, improving microcirculation, and inhibiting thrombosis in arteries and veins; it also has multiple functions such as lowering blood sugar and blood pressure.

Cephalexin is a first-generation cephalosporin with an antibacterial spectrum similar to that of cephalothin, but its antibacterial activity is poorer than that of the latter. Except for Enterococcus and methicillin-resistant Staphylococci, most strains of Streptococcus pneumoniae, hemolytic Streptococcus, and Staphylococcus aureus that produces or does not produce penicillinase are sensitive to this product. This product has a good antibacterial effect on Neisseria, but Haemophilus influenzae is less sensitive to this product; this product has a certain antibacterial effect on some Escherichia coli, Proteus mirabilis, Salmonella and Shigella. The remaining Enterobacteriaceae, Acinetobacter, Pseudomonas aeruginosa, and Bacteroides fragilis are resistant to this product. Fusobacterium and Veillonella are generally sensitive to this product, and anaerobic Gram-positive cocci are moderately sensitive to this product.

This product can inhibit viral DNA and RNA polymerase, thereby inhibiting viral reproduction. On human embryonic kidney cells, 1% concentration has a significant inhibitory effect on DNA viruses (adenovirus, herpes virus) and RNA viruses (echovirus), and has an inhibitory effect on all stages of the viral proliferation cycle. It has no direct effect on free viral particles.

It can inhibit the synthesis of prostaglandins and has antipyretic and analgesic effects

It is a central nervous system stimulant that can enhance the antipyretic and analgesic effects of acetaminophen and reduce central nervous system inhibitory effects such as drowsiness and dizziness caused by other drugs.

It is an antihistamine that can relieve runny nose, nasal congestion, and sneezing symptoms.

It has antipyretic and sedative effects

This product can directly penetrate the cell membrane into the body cells, activate pyruvate oxidase, so that cells in a low-energy and hypoxic state can continue to metabolize smoothly, and participate in the energy metabolism and protein synthesis of the human body.

This product can directly penetrate the cell membrane into the body cells, activate pyruvate target=_blank oxidase, so that the cells in the low-energy hypoxia state can continue to metabolize smoothly, and participate in the energy metabolism and protein synthesis of the human body.

This product can directly penetrate the cell membrane into the body cells, activate pyruvate target=_blank oxidase, so that the cells in the low-energy hypoxia state can continue to metabolize smoothly, and participate in the energy metabolism and protein synthesis of the human body.

This product can directly penetrate the cell membrane into the body cells, activate pyruvate target=_blank oxidase, so that the cells in the low-energy hypoxia state can continue to metabolize smoothly, and participate in the energy metabolism and protein synthesis of the human body.

This product can directly penetrate the cell membrane into the body cells, activate pyruvate target=_blank oxidase, so that the cells in the low-energy hypoxia state can continue to metabolize smoothly, and participate in the energy metabolism and protein synthesis of the human body.