「Vancomycin」の共起表現(1語左で並び替え)

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共起表現

「Vancomycin」の共起表現一覧(1語左で並び替え)

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, ranitidine, triamterene, trimethoprim, and	vancomycin) and certain drugs tend to produce hyperglyc
e with the current “last defence” antibiotic	vancomycin.
ical drugs, including the natural antibiotic	vancomycin, the antihistamine loratadine (Claritin), th
coming resistant against such antibiotics as	vancomycin.
It belongs to the same class as	vancomycin, the most widely-used and one of the few tre
e natural glycopeptides currently available,	vancomycin and teicoplanin.
The original indication for	vancomycin was for the treatment of penicillin-resistan
Several derivatives of	vancomycin are currently being developed, including ori
use of cloxacillin may permit reduced use of	vancomycin.
istically non-inferior to the combination of	vancomycin and ceftazidime for the treatment of skin an
This binding of	vancomycin to the D-Ala-D-Ala prevents the incorporatio
residue has been replaced by a D-lactate, so	vancomycin cannot bind.
Possessing longer half-lives than	vancomycin, these newer candidates may demonstrate impr
etrating into leucocytes and phagocytes than	vancomycin.
It is more lipophillic than	vancomycin, as it has more fatty acid chains.
to be 50 to 100 times more lipophillic than	vancomycin.
It can be two to four times more active than	vancomycin, but it does depend upon the organism.
strates an inherent, low level resistance to	vancomycin.
lanin has an increased half life compared to	vancomycin, as well as having better tissue penetration
n-inferior efficacy against MRSA compared to	vancomycin and aztreonam Recently, ceftaroline has comp

共起表現

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「Vancomycin」の共起表現一覧(1語左で並び替え)