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46 Cards in this Set

  • Front
  • Back
Narrow spectrum penicillins
-Benzyl penicillins
-Penicillin V
Broad spectrum penicillins
-Ampicillin
-Amoxicillin
Anti-Staph Penicillins
-flucoxacillin
-methicillin
-oxacillin
Anti Pseud. penicillins
-ticarcillin
-piperacillin
Penicillin given orally
-penicilllin V
-ampicillin and flucoxacillin
Penicillin given IV
-penicillin G
-all others apart from ampicillin and flucoxacillin and penicillin V
Competes for tubular secretion in kidney with penicillin
Probenecid
Cefuroxime
2nd class (injectable) of cephalosporins used against gram positive bact such as e.coli and some proteus species
Cefotaxime
3rd class, newer injectable cephalosporin, used against gram -ve bact and strep
ceftriaxone
3rd class, newer injectable cephalosporin, used against gram -ve bact and strep
ceftazidime
5th class, antipseudomonal (broad spectrum)
imiperem
-carbapenems
-antipseudomonal effects
-broad spectrum inc. anti anearobes
-given IV
monoperum
-carbapenems
-antipseudomonal effects
-broad spectrum inc. anti anearobes
-given IV
carbapenems
-broad spectrum inc. anti anearobes
-given IV
-eg. ertapenem, doripenem
monobactems
-broad spectrum inc. anti anearobes
-given IV
-eg. aztreonam
gentamicin
-aminoglycoside
-used against many bact infections but esp. gram -ve bact but not: n. gonorrhea or menigitidis and legionella pneumophilia
aminoglycosides
-life saving
-toxic to kidney and 8th cranial nerve at high levels
-prevent translation of mRNA into protiens
gentamicin combinatoral use for endocarditis: gentamicin+....
-strep=penicillin
-staph=flucoxacillin
-enterococcal=amoxicillin
aminoglycosides examples
-streptomycin (derived from streptomyces)
-tobramycin
-netimicin
-amikacin
-neomycin
-spectriomycin
macrolides active against:

used for:
-gram +ve cocci, mycoplasma, anaerobes (NOT bacteriodes), chlamydia
-1st line of defence against pneaumonia
-instead of penicillin for: URTI and skin and soft tissue infections
erythromycin
-macrolide:
-crosses placenta, binds to 50s ribosome to interfere with protein synthesis, concentrated in macrophages, polymorphs and liver
macrolides: absorption and excretion
-oral absorption, distributed in total body water
-excreted in bile
clarithromycin
-macrolide:
-crosses placenta, binds to 50s ribosome to interfere with protein synthesis, concentrated in macrophages, polymorphs and liver
azithromycin
-macrolide:
-crosses placenta, binds to 50s ribosome to interfere with protein synthesis, concentrated in macrophages, polymorphs and liver
clindamycin
-lincosamide:
-interferes with protein synthesis and blocks M protein production that leads to an inflam response so can be used in TSS
-used against staph and strep
lincomycin
-lincosamide:
-interferes with protein synthesis and blocks M protein production that leads to an inflam response so can be used in TSS
-used against staph and strep
How to take tetracyclines
-on an empty stomach as the bind to dairy products so cant be absorbed
tetracyclines active against:
-many gram +ves
-some gram -ves: treponemes, mycoplasma, rickettsia, chlamydia
tetracycline distribution
-liver, lungs, kidney, brain and resp tract
-concentrated in bile
tetracycline mechanism
-locks tRNA and mRNA affecting protein synthesis
group 1 tetracycline
-tetracycline
-oxytetracycline
group 2 tetracycline
-methacycline
-demeclocycline
group 3 tetracycline
-doxycycline
-minocycline
Quinolones
-inhibit DNA gyrase
-well absorbed orally
-widely distributed and can penetrate cell walls
quinolones used against:
-gram +ve agents such as strep pneumoniae, mycobacterium TB
4th generation quinolones
trovafloxacin
moxifloxacin
vancomycin
-glycopeptide
-essential MRSA bacteraemia and device infection treatment
-resistance rare in enterococcus faecalis
-potential nephrotoxicity and otoxicity
-antibiotic monitoring essential
teicoplanin
-glycopeptide
-outpatient therapy for joint and bone infections
-device related infections
glycopeptides administration and excretion
-administered IV or peritoneally
-excreted by kidneys
-crosses BBB if inflammed
glycopeptides action mechanism
-inhibits peptidoglycan cross linking in gram +ve organisms only
trimethoprim
-micellaneous agent
-used in treatment of malaria
-inhibits tetrahydrofolate synthesis
metrodiazole mechanism of action
-micellaneous agent
-accepts e- under anaerobic conditions and forms toxic metabolites that damage bact DNA
-used against anaerobes
metrodiazole administration and excretion
-orally or parenterally
-met. by liver and excreted by kidney
-crosses BBB so can penetrate abscesses
oxazolidinones
-linezolid
-gram +ve bact.
-inhibit protein synthesis at 50s ribosome
lipopeptides
-disrupts cell membrane of gram +ve bacteria
treatment for bact menigitis
-alert authrorities
-IV cefotaxime
-IV ceftriaxone