Примери за използване на Aeruginosa на Английски и техните преводи на Български
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helps to differentiate the organism from P. aeruginosa.
Colobreathe is used to manage long-term lung infection caused by the bacteria Pseudomonas aeruginosa in patients aged six years
This is of a direct concern of Gram-negative non-fermenters facing Acinetobacter baumannii and Pseudomonas aeruginosa.
Phenotypic and genetic characteristics of antibiotic resistance to carbapenems in Acinetobacter baumannii and Pseudomonas aeruginosa- Medical Review(Medicinski pregled), 52, 2016,№ 2, 5-14.
Colobreathe is indicated for the management of chronic pulmonary infections due to Pseudomonas aeruginosa in patients with cystic fibrosis(CF)
Cayston is indicated for the suppressive therapy of chronic pulmonary infections due to Pseudomonas aeruginosa in patients with cystic fibrosis(CF)
Concomitant use of an aminoglycoside may be indicated when Pseudomonas aeruginosa infections are suspected or proven to be involved in the approved indications(see section 4.1).
chronic pseudomonas aeruginosa infection.
Concomitant use of an aminoglycoside may be indicated when Pseudomonas aeruginosa infections are suspected or proven to be involved in the approved indications(see section 4.1).”.
Almost 95% of MOE cases reported in the literature are attributed to Pseudomonas aeruginosaBovo et al.
Because the number of patients with cystic fibrosis and P. aeruginosa bacterial lung infection is low,
while for the treatment of complicated UTI due to Pseudomonas aeruginosa at least a dose of 500 mg bid of ciprofloxacin is needed(equivalent to 400 mg intravenous twice daily).
more subsets of the paediatric population in cystic fibrosis patients with Pseudomonas aeruginosa pulmonary infection/colonisation(see section 4.2 for information on paediatric use).
biofilms are present in the chronic Pseudomonas aeruginosa and Burkholderia cenocepacia infections characteristic of cystic fibrosis.[21].
increases were observed in the MIC90 for all P. aeruginosa isolates as well as in the percentages of patients with P. aeruginosa resistant(MIC above the parenteral breakpoint)
more subsets of the paediatric population in Pseudomonas aeruginosa pulmonary infection/colonisation in patients with cystic fibrosis(see section 4.2 for information on paediatric use).
Pseudomonas aeruginosa: Negative to test.
Aeruginosa is a frequent cause of infections in cystic fibrosis patients.
Most often the causative agent of this disease is Pseudomonas aeruginosa.
Bacterial lung infection with P. aeruginosa is frequent in cystic fibrosis patients.