This product belongs to the third generation of cephalosporin, has a broad-spectrum antibacterial effect, and is stable to β-lactamase produced by most bacteria. This product is mainly effective against a variety of G and G- bacteria and anaerobic bacteria. It has an immunomodulatory effect, that is, it can be used as a biological response modifier (BRM) to increase CD4 in the body, thereby increasing the CD4/CD8 value and playing a synergistic bactericidal effect. The mechanism of action of this product is that this product achieves a bactericidal effect by inhibiting the biosynthesis of bacterial cell wall mucopeptides.

This product belongs to the third generation of cephalosporin, with a broad-spectrum antibacterial effect, and is stable to β-lactamase produced by most bacteria. This product is mainly effective against a variety of G+ and G- bacteria and anaerobic bacteria. It has an immunomodulatory effect, that is, it can be used as a biological response modifier (BRM) to increase CD4 in the body, thereby increasing the CD4/CD8 value and playing a synergistic bactericidal effect. This product is ineffective against Bacteroides, Acinetobacter, Enterococcus faecalis, Listeria, Mycoplasma, and Chlamydia. The mechanism of action of this product is that this product achieves a bactericidal effect by inhibiting the biosynthesis of bacterial cell wall mucopeptides.

Dispel wind and relieve pain, aromatic and clear the orifices, relieve itching and swelling

Dispel wind and relieve pain, aromatic and clear the orifices, relieve itching and swelling

Dispel wind and relieve pain, aromatic and clear the orifices, relieve itching and swelling

Dispel wind and relieve pain, aromatic and clear the orifices, relieve itching and swelling

Dispel wind and relieve pain, aromatic and clear the orifices, relieve itching and swelling

This product is a proton pump inhibitor of gastric parietal cells. It is rapidly activated under strong acidic conditions and can specifically inhibit the secretory microtubules and tubular vesicles in the cytoplasm of the parietal cell apical membrane, causing irreversible inhibition of the enzyme, thereby effectively inhibiting the secretion of gastric acid. It can not only non-competitively inhibit the gastric acid secretion caused by gastrin, histamine, and choline, but also inhibit some basic gastric acid secretions that are not affected by choline or H2 receptor blockers. This product is metabolized through the first system of the cytochrome P450 enzyme system in hepatocytes, and can also be metabolized through the second system, with the advantage of small drug interactions. It has no mutagenic, carcinogenic, and teratogenic effects.