High performance antibiotic medicine composition
A technology of antibacterial drugs and compositions, which is applied in the field of high-efficiency antibacterial drug compositions, can solve the problems of no azlocillin sodium and tazobactam, achieve good chemical stability, be easy to popularize and apply, and enhance the effect of antibacterial activity
Patent Information
- Authority / Receiving Office
- CN · China
- Current Assignee / Owner
- Publication Date
- 2005-03-02
- Estimated Expiration
- Not applicable · inactive patent
Abstract
Description
Technical field
[0001] The present invention relates to a high-efficiency antibacterial pharmaceutical composition, and more specifically to a high-efficiency antibacterial pharmaceutical composition containing azlocillin sodium and tazobactam. Background technique
[0002] As we all know, due to the long-term and large-scale use of antibiotics in clinical practice, bacteria have become more and more resistant to antibiotics. For example, bacterial meningitis, otitis media, sepsis and pneumonia caused by Streptococcus pneumoniae are important pathogens. , Is the main pathogenic bacteria of children's out-of-hospital infections, and the first pathogenic bacteria for community infections in adults, especially the elderly. Because Streptococcus pneumoniae has developed resistance to penicillin and other β-lactam antibiotics, the 1990s Since penicillin-resistant Streptococcus pneumoniae has spread widely around the world, the therapeutic effect of the drug ...
Examples
Embodiment 1
[0029] Take 1.0 g of azlocillin sodium and 10.0000 g of tazobactam, mix them, and pack them in a 100-grade clean area with a relative humidity below 45% and meet the requirements of GMP.
Embodiment 2
[0031] Take 2.0 g of azlocillin sodium and 0.2000 g of tazobactam, mix them, and pack them in a 100-class clean area with a relative humidity of 45% or less and meeting GMP requirements.
Embodiment 3
[0033] Take 1.0 g of azlocillin sodium and 1.0000 g of tazobactam, mix them, and pack them in a 100-class clean area with a relative humidity of 45% or less and meeting GMP requirements.