This product is a blood lipid regulating drug of clofibric acid derivatives. Its mechanism of lowering blood lipids is not yet fully understood. It may reduce the cAMP content in liver microsomes, increase the activity of lipoprotein esterase, and decompose lipids in lipoproteins. Experimental and clinical studies have shown that this product reduces blood cholesterol and triglycerides and increases blood high-density lipoprotein. In addition, this product also has anti-platelet aggregation and anti-thrombotic effects and reduces blood uric acid.

It is a diuretic, diuretic, and jaundice-relieving drug.

Clears away heat and dries dampness, promotes dampness and reduces jaundice, while rhubarb and mirabilite are laxatives and laxatives. They are both assistant drugs

Clears away heat and dries dampness, promotes dampness and reduces jaundice, while rhubarb and mirabilite are laxatives and laxatives. They are both assistant drugs

It has laxative effect and is a ministerial drug.

It has laxative effect and is a ministerial drug.

Soothes the liver and gallbladder, promotes qi and relieves pain. Betel nut promotes qi and diuresis and is also an adjuvant

Soothes the liver and gallbladder, promotes qi and relieves pain. Betel nut promotes qi and diuresis and is also an adjuvant

Soothes the liver and gallbladder, promotes qi and relieves pain. Betel nut promotes qi and diuresis and is also an adjuvant

Soothes the liver and gallbladder, promotes qi and relieves pain. Betel nut promotes qi and diuresis and is also an adjuvant

It is also an assistant to promote qi and diuresis

This product is a replacement product of the macrolide antibiotic erythromycin. Its mechanism of action is to bind to the 70 ribosome 50 subunit of the bacterial cell, hindering the synthesis of bacterial protein, thereby inhibiting the bacteriostasis, and has excellent broad-spectrum antibacterial efficacy. This product is particularly sensitive to Gram-positive bacteria and effective against penicillin-resistant bacteria. It is used for infections such as beta-hemolytic streptococci, Staphylococcus aureus, pneumococcus, influenza bacilli, Listeria, diphtheria bacilli, and pertussis bacilli. It has a good bactericidal effect on some pathogens that are ineffective against penicillins and cephalosporins, such as Legionella, Chlamydia, Mycoplasma and other atypical pathogens.

This product is an antiviral drug. It has an inhibitory effect on herpes simplex virus, varicella zoster virus, cytomegalovirus, etc. in vitro. After entering the cells infected by herpes virus, this product competes with deoxynucleoside for viral thymidine kinase or cell kinase, and the drug is phosphorylated into activated acyclovir triphosphate, and then inhibits viral replication in two ways: ① Interfering with viral DNA polymerase and inhibiting viral replication; ② Under the action of DNA polymerase, it binds to the growing DNA chain, causing the extension of the DNA chain to be interrupted. This product has a special affinity for viruses, but has low toxicity to mammalian host cells.