Harbin Pharmaceutical Group Co., Ltd. GENERAL Pharm. FACTORY

It is a third-generation cephalosporin antibiotic with strong activity against Enterobacteriaceae, and has a strong antibacterial effect on Escherichia coli, Klebsiella pneumoniae, Enterobacter aerogenes, etc. It has a strong antibacterial effect on Haemophilus influenzae, Neisseria gonorrhoeae and Neisseria meningitidis, and also has a good effect on hemolytic streptococci and pneumococci; the MIC for Staphylococcus aureus is 2-4 mg/L, methicillin-resistant Staphylococci and enterococci are resistant to this product, and most Bacteroides fragilis are resistant to this product.

It works by inhibiting the biosynthesis of cell wall mucopolypeptides and is effective against Gram-positive aerobic microorganisms (such as faecal streptococci, Staphylococci, Streptococcus pneumoniae, Streptococci) and some Gram-negative aerobic microorganisms.

It can inhibit the beta-lactamase produced by most bacteria and restore the sensitivity of bacteria to amoxicillin.

It is a bactericidal broad-spectrum antibiotic. When used in combination with sulbactam sodium, it can be protected from destruction by β-lactamase and has a bactericidal effect on a variety of Gram-positive and Gram-negative bacteria.

Irreversible broad-spectrum β-lactamase inhibitor that protects amoxicillin from destruction by β-lactamases and enhances its effectiveness against enzyme-producing resistant bacteria.

Amoxicillin is a bactericidal broad-spectrum antibiotic. Due to the presence of sulbactam sodium, amoxicillin can be protected from the destruction of β-lactamase, thus making it sensitive to bacteria that are resistant to amoxicillin and produce β-lactamase. This product is a bactericidal antibiotic that can kill a variety of Gram-positive and Gram-negative bacteria in clinical practice.

Sulbactam sodium is an irreversible broad-spectrum β-lactamase, which can make amoxicillin lose its antibacterial activity. By inhibiting β-lactamase, sulbactam sodium protects amoxicillin from being destroyed and enhances its antibacterial effect, especially against drug-resistant bacteria that produce β-lactamase.

This product is an acetanilide antipyretic analgesic. It inhibits the prostaglandin synthase in the hypothalamic temperature regulation center, reduces the synthesis and release of prostaglandin PGE1, causes peripheral vasodilation and sweating, and achieves an antipyretic effect. Its antipyretic effect is similar to that of aspirin; it inhibits the synthesis and release of prostaglandin PGE1, bradykinin and histamine, increases the pain threshold and has an analgesic effect. It is a peripheral analgesic, weaker than aspirin, and is only effective for mild and moderate pain. This product has no obvious anti-inflammatory effect.