oxazolidinones and fusidic acid Flashcards
what is the moa of oxazolidinones
they inhibit protein synthesis
by binding 23S of 50S thus preventing formation of 70S initiation complex thats imp for translation process
lindezolid is bacteriostatic against Enterococci and staphylcocci
and is bactericidal against streptococci
whats something special about tedizolid
its inactive until its in vivo and dephospharlayted
its structure allows it for tighter binding to the ribosome thus higher potency
antibacterial spec of oxazolidinones
1) Gram +ve cocci
Streptococci , staphylcocci (MRSA), enterococci (VRE)
2) Gram +VE rods
-L. monocytogenes , Bacillus , corynebacterium
3) M. tuberculosis
indications of oxazolidinones
linezolid:
- empiric therapy or due to MRSA or VRE
- Bacteraemia
- pneumonia
-diabetic foot infection
-complicated UTI
-Skin and soft tissue infection (both drugs)
indications of oxazolidinones
linezolid:
- empiric therapy or due to MRSA or VRE
- Bacteraemia
- pneumonia
-diabetic foot infection
-complicated UTI
-Skin and soft tissue infection (both drugs)
AE of oxazolidinones
GI effects , headache , rash
anemia , leukopenia and thromocytopenia
fusidic acid
natural antibitoic that has a steroidal structure doesnt posses any steroidal activity
merely has high penetration power due to steroidal nature
FA mOA
It has bacteriostatic and bactericidal activity mainly against Gram +ve
inhibits protein synthesis by blocking aminoacyl-tRNA transfer to protein
FA antibacterial spec
S. aureus
Gram +ve anaerobes
-C.diff , M. leparae
Streptococci are resistant
indications of FA
Staphylococcal infections (not used as mono therpay but combined with other antistaph agents or else resistance occurs)
Skin and eye infections ( topical )