Beta Lactam Flashcards
Penicillin G
Penicillin
Penicillins
Penicillin G Penicillin V Benzathine penicillin Procaine penicillin Nafcillin Oxacillin Ampicillin Amoxicillin Ticarcillin Piperacillin
Penicillin V
Penicillin
Benzathine penicillin
Penicillin
Procaine penicillin
Penicillin
Nafcillin
Penicillin
Oxacillin
Penicillin
Ampicillin
Penicillin
Amoxicillin
Penicillin
Ticarcillin
Penicillin
Piperacillin
Penicillin
Penicillin V
Oral low systemic levels limit widespread use
Oral low systemic levels limit widespread use
Penicillin V
Benzathine penicillin
Intramuscular, long-acting formulations
Intramuscular, long-acting formulations
Benzathine penicillin
Procaine penicillin
Procaine penicillin
Intramuscular, long-acting formulations
Intramuscular, long-acting formulations
Procaine penicillin
Benzathine penicillin
Nafcillin
Intravenous, added stability to staphylococcal beta lactamase, billiary clearance
Intravenous, added stability to staphylococcal beta lactamase, billiary clearance
Nafcillin
Oxacillin
Oxacillin
Intravenous, added stability to staphylococcal beta lactamase, billiary clearance
Intravenous, added stability to staphylococcal beta lactamase, billiary clearance
Oxacillin
Nafcillin
Ampicillin, amoxicillin, ticarcillin, piperacillin
Greater activity versus gram-negative bacteria; addition of beta lactamase inhibitor restores activity against many beta lactamase-producing bacteria
Greater activity versus gram-negative bacteria; addition of beta lactamase inhibitor restores activity against many beta lactamase-producing bacteria
Ampicillin, amoxicillin, ticarcillin, piperacillin
Penicillin G
Mechanism of action
Prevents bacterial cell wall synthesis by binding to and inhibiting cell wall transpeptidases
Prevents bacterial cell wall synthesis by binding to and inhibiting cell wall transpeptidases
Penicillin G
Mechanism of action
Penicillin G
Effects
Rapid bactericidal activity against susceptible bacteria
Rapid bactericidal activity against susceptible bacteria
Penicillin G
Effects
Penicillin G
Clinical applications
Streptococcal infections
Meningococcal infections
Neurosyphilis
Streptococcal infections, meningococcal infections, neurosyphilis
Penicillin G
Clinical applications
Penicillin G
Pharmacokinetics, toxicities, interactions
IV administation
Rapid renal clearance (half-life 30 min, so requires frequent dosing (every 4)
Toxicity: Immediate hypersensitivity, rash, seizures
IV administation
Rapid renal clearance (half-life 30 min, so requires frequent dosing (every 4)
Toxicity: Immediate hypersensitivity, rash, seizures
Penicillin G
Pharmacokinetics, toxicities, interactions
Cephalosporins
Cefazolin Cephalexin Cefuroxime Cefotetan Cefoxitin Ceftriaxone Cefotaxime Ceftazidime Cefepime
Cefazolin
Cephalosporin
Cephalexin
Cephalosporin
Cefuroxime
Cephalosporin
Cefotetan
Cephalosporin
Cefoxitin
Cephalosporin
Ceftriaxone
Cephalosporin
Cefotaxime
Cephalosporin
Ceftazidime
Cephalosporin
Cefepime
Cephalosporin
Cefazolin
Mechanism of action
Preventa bacterial cell wall synthesis by binding to and inhibiting cell wall transpeptidases
Prevents bacterial cell wall synthesis by binding to and inhibiting cell wall transpeptidases
Cefazolin
Mechanism of action
Cefazolin
Effects
Rapid bactericidal activity against susceptible bacteria
Rapid bactericidal activity against susceptible bacteria
Cefazolin
Effects
Cefazolin
Clinical applications
Skin and soft tissue infections
Urinary tract infections
Surgical prophylaxis
Skin and soft tissue infections
Urinary tract infections
Surgical prophylaxis
Cefazolin
Clinical applications
Cefazolin
Pharmacokinetics, toxicities, interactions
IV administration Renal clearance (half-life 1.5 h) Dosed every 8 h Poor penetration into the CNS Toxicity: rash, drug fever
IV administration Renal clearance (half-life 1.5 h) Dosed every 8 h Poor penetration into the CNS Toxicity: rash, drug fever
Cefazolin
Pharmacokinetics, toxicities, interactions
Caphalexin
Oral, first generation drug, used for treating skin and soft tissue infections and urinary tract infections
Oral, first generation drug, used for treating skin and soft tissue infections and urinary tract infections
Cephalexin
Cefuroxime
Oral and intravenous, second generation drug, improved activity versus Pneumococcus and Haemophilus Influenzae
Oral, first generation drug, used for treating skin and soft tissue infections and urinary tract infections
Cefuroxime
Cefotetan, cefoxitin
Intravenous, second generation drugs, activity versus Bacteroides fragilis allows for use in abdominal/pelvic infections
Intravenous, second generation drugs, activity versus Bacteroides fragilis allows for use in abdominal/pelvic infections
Cefotetan, cefoxitin
Ceftriaxone
Intravenous, third generation drug, mixed clearance with long half-life (6 hours), good CNS penetration, many uses including pneumonia, meningitis, pyelonephritis, and gonorrhea
Intravenous, third generation drug, mixed clearance with long half-life (6 hours), good CNS penetration, many uses including pneumonia, meningitis, pyelonephritis, and gonorrhea
Ceftriaxone
Cefotaxime
Intravenous, third generation, similar to ceftriaxone; however, clearance is renal and half-life is 1 hour
Intravenous, third generation, similar to ceftriaxone; however, clearance is renal and half-life is 1 hour
Cefotaxime
Ceftazidime
Intravenous, third generation drug, poor gram positive avtivity, good activity versus Pseudomonas
Intravenous, third generation drug, poor gram positive avtivity, good activity versus Pseudomonas
Ceftazidime
Cefepime
Intravenous, fourth generation drug, broad activity with improved stability to chromosomal beta lactamase
Intravenous, fourth generation drug, broad activity with improved stability to chromosomal beta lactamase
Cefepime
Carbapenems
Imipenem-cilastatin
Meropenem
Doripenem
Ertapenem
Imipenem-cilastatin
Carbapenem
Meropenem
Carbapenem
Doripenem
Carbapenem
Ertapenem
Carbapenem
Imipenem-cilastatin
Mechanism of action
Prevents bacterial cell wall synthesis by binding to and inhibting cell wall transpeptidases
Prevents bacterial cell wall synthesis by binding to and inhibting cell wall transpeptidases
Imipenem-cilastatin
Mechanism of action
Imipenem-cilastatin
Effects
Rapid bactericidal activity against susceptible bacteria
Rapid bactericidal activity against susceptible bacteria
Imipenem-cilastatin
Effects
Imipenem-cilastatin
Clinical applications
Serious infections such as pneumonia and sepsis
Serious infections such as pneumonia and sepsis
Imipenem-cilastatin
Clinical application
Imipenem-cilastatin
Pharmacokinetics, toxicities, interactions
IV administration Renal clearance (half-life 1 h), dosed every 6-8 h, cilastatin added to prevent hydrolysis by renal dehydropeptidase Toxicity: Seizures especially in renal failure or wih high doses (> 2 g/d)
IV administration Renal clearance (half-life 1 h), dosed every 6-8 h, cilastatin added to prevent hydrolysis by renal dehydropeptidase Toxicity: Seizures especially in renal failure or wih high doses (> 2 g/d)
Imipenem-cilastatin
Pharmacokinetics, toxicities, interactions
Meropenem, doripenem
Intravenous, similar activity to imipenem; stable to renal dehydropeptidase, lower incidence serizures
Intravenous, similar activity to imipenem; stable to renal dehydropeptidase, lower incidence serizures
Meropenem, doripenem
Ertapenem
Intravenous, longer half-life allows for once daily dosing, lacks activity versus pseudomonas and acinetobacter
Intravenous, longer half-life allows for once daily dosing, lacks activity versus pseudomonas and acinetobacter
Ertapenem
Monobactams
Aztreonam
Aztreonam
Monobactam
Aztreonam
Mechanism of action
Prevents bacterial cell wall synthesis by binding to and inhibiting cell wall transpeptidases
Prevents bacterial cell wall synthesis by binding to and inhibiting cell wall transpeptidases
Aztreonam
Mechanism of action
Aztreonam
Effects
Rapid bactericidal activity against susceptible bacteria
Rapid bactericidal activity against susceptible bacteria
Aztreonam
Effects
Aztreonam
Clinical applications
Infections caused by aerobic, gram-negative bacteria in patients with immediate hypersensitivty to penicillins
Infections caused by aerobic, gram-negative bacteria in patients with immediate hypersensitivty to penicillins
Aztreonam
Clinical applications
Aztreonam
Pharmacokinetics, toxicities, interactions
IV administration
Renal clearance half-life 1.5 h
Dosed every 8 h
Toxicity: no crossallergenicity with penicillins
IV administration
Renal clearance half-life 1.5 h
Dosed every 8 h
Toxicity: no crossallergenicity with penicillins
Aztreonam
Pharmacokinetics, toxicities, interactions