Antibacterial Agents III Flashcards
The three macrolides are ___________.
azithromycin, clarithromycin, and erythromycin
What are the important considerations for hepatically metabolized drugs?
(1) drug-drug interactions; (2) genetic differences in metabolism; and (3) potential for hepatotoxicity
All of the protein-synthesis inhibitors are bacteriostatic except __________.
the aminoglycosides, which irreversibly bind to the 30S subunit
The tetracyclines bind to the _________, as do aminoglycosides.
30S subunit
Chloramphenicol and the macrolides bind to the ____________.
50S subunit
Resistance to tetracycline is commonly accomplished by _________.
acquisition of DNA that expresses proteins for efflux pumps
Tetracycline absorption is impaired by _________.
milk products, Al3+, Ca2+, Mg2+, and Fe2+
Chemically, macrolides are __________.
weak bases that are more active at alkaline pHs
Drug inactivation does not occur with __________.
macrolides
Resistance to macrolides can occur by _________.
drug efflux or methylation of the 50S subunit
Which macrolide should be taken on an empty stomach?
Azithromycin
Azithromycin and erythromycin cannot reach the _______, but they can pass to the ________.
CSF; placenta
Which macrolide can be dosed once daily?
Azithromycin
Macrolides can kill ____________.
Gram-positive cocci (except enterococci), many Gram-negative bacteria (H. influenzae, Neisseria, Leionella, Bortadella), and atypical bacteria
What are the three ways bacteria become resistant to tetracyclines?
Decreased entry, increased efflux, and modified protein target (30S)