Doripenem hydrate is a parenteral, potent, and composed antibacterial adjoin a growthd
ambit of both Gram+ and Gram- bacilli including Pseudomonas aeruginosa with
MIC90 ethics of ≤ 0.5 µg/ml adjoin
methicillin-susceptible streptococci and staphylococci, 0.032-0.5 µg/ml adjoin
associates of the ancestors Enterobacteriaceae, Moraxella catarrhalis, and
Haemophilus influenza, and 8 µg/ml adjoin Pseudomonas aeruginosa.
Patients
with cystic fibrosis can be adulterated with several bacilli such as
Haemophilus influenzae, Staphylococcus aureus and P. aeruginosa, chronically.
By 18 years of age, 80% of cystic fibrosis patients are adulterated with P.
aeruginosa.
Doripenem
hydrate was almighty adjoin Staphylococcus aureus and Staphylococcus
epidermidis with the aforementioned MIC90 amount of 0.063 µg/ml. Doripenem
hydrate was 2-4 times added alive than added activated carbapenems adjoin S. aureus.
The action of doripenem hydrate adjoin S. pneumoniae was agnate to that of
imipenem but college than that of added activated agents. Doripenem hydrate was
almighty adjoin S. pneumonia with an action agnate to that of added activated
carbapenems (MIC90, 0.5 µg/ml). Doripenem hydrate had an action agnate to that
of cefpirome adjoin S. pneumoniae and S. pyogenes. Doripenem hydrate was added
alive adjoin Enterococcus faecalis than added activated agents except for
imipenem.
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