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Infectious Diseases
Bacteria and Antibacterial Drugs
β-Lactams
Cephalosporins
Pharmacology
Indications
First-generation cephalosporins
Second-generation cephalosporins and cephamycins
Third-generation cephalosporins
Fourth-generation cephalosporin
Fifth-generation cephalosporin
Contraindications
Use During Pregnancy and Breastfeeding
Adverse Effects
Contraindications
Penicillins
Pharmacology
Indications
Amoxicillin and ampicillin
Penicillinase-resistant penicillins
Broad-spectrum (antipseudomonal) penicillin
Contraindications
Use During Pregnancy and Breastfeeding
Adverse Effects
Hypersensitivity
Rashes
Other adverse effects
Dosing Considerations
Other β-Lactams
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β-Lactams

inShare0

β-Lactams are antibiotics that have a β-lactam ring nucleus. Subclasses include

  • Cephalosporins and cephamycins (cephems)
  • Carbacephems (loracarbef Some Trade Names
    LORABID

    )
  • Penicillins
  • Clavams
  • Carbapenems
  • Monobactams

All β-lactams bind to and inactivate enzymes required for bacterial cell wall synthesis.

Cephalosporins

Cephalosporins are bactericidal (Table 7: Cephalosporins*Tables). They inhibit enzymes in the cell wall of susceptible bacteria, disrupting cell synthesis.

Table 7

PrintOpen table Open table in new window
Cephalosporins*

Drug

Route

1st Generation

Cefadroxil Some Trade Names
DURICEF
Click for Drug Monograph

Oral

Cefazolin Some Trade Names
ANCEF
KEFZOL
Click for Drug Monograph

Parenteral

Cephalexin Some Trade Names
KEFLEX
KEFTAB
Click for Drug Monograph

Oral

Cephradine

Oral

2nd Generation

Cefaclor Some Trade Names
CECLOR
Click for Drug Monograph

Oral

Cefotetan Some Trade Names
CEFOTAN
Click for Drug Monograph

Parenteral

Cefoxitin Some Trade Names
MEFOXIN
Click for Drug Monograph

Parenteral

Cefprozil Some Trade Names
CEFZIL
Click for Drug Monograph

Oral

Cefuroxime Some Trade Names
CEFTIN
ZINACEF
Click for Drug Monograph

Parenteral or oral

Loracarbef Some Trade Names
LORABID

Oral

3rd Generation

Cefdinir Some Trade Names
OMNICEF
Click for Drug Monograph

Oral

Cefditoren

Oral

Cefixime Some Trade Names
SUPRAX
Click for Drug Monograph

Oral

Cefoperazone

Parenteral

Cefotaxime Some Trade Names
CLAFORAN
Click for Drug Monograph

Parenteral

Cefpodoxime Some Trade Names
VANTIN
Click for Drug Monograph

Oral

Ceftazidime Some Trade Names
FORTAZ
TAZICEF
Click for Drug Monograph

Parenteral

Ceftibuten Some Trade Names
CEDAX
Click for Drug Monograph

Oral

Ceftizoxime Some Trade Names
CEFIZOX

Parenteral

Ceftriaxone Some Trade Names
ROCEPHIN
Click for Drug Monograph

Parenteral

4th Generation

Cefepime Some Trade Names
MAXIPIME
Click for Drug Monograph

Parenteral

5th Generation

Ceftobiprole

Parenteral

*Loracarbef Some Trade Names
LORABID

is technically a carbacephem, and cefoxitin Some Trade Names
MEFOXIN
Click for Drug Monograph
and cefotetan Some Trade Names
CEFOTAN
Click for Drug Monograph
are technically cephamycins, but they are grouped with cephalosporins because of similar antimicrobial spectra and pharmacology.

Cephalosporins*

Drug

Route

1st Generation

Cefadroxil Some Trade Names
DURICEF
Click for Drug Monograph

Oral

Cefazolin Some Trade Names
ANCEF
KEFZOL
Click for Drug Monograph

Parenteral

Cephalexin Some Trade Names
KEFLEX
KEFTAB
Click for Drug Monograph

Oral

Cephradine

Oral

2nd Generation

Cefaclor Some Trade Names
CECLOR
Click for Drug Monograph

Oral

Cefotetan Some Trade Names
CEFOTAN
Click for Drug Monograph

Parenteral

Cefoxitin Some Trade Names
MEFOXIN
Click for Drug Monograph

Parenteral

Cefprozil Some Trade Names
CEFZIL
Click for Drug Monograph

Oral

Cefuroxime Some Trade Names
CEFTIN
ZINACEF
Click for Drug Monograph

Parenteral or oral

Loracarbef Some Trade Names
LORABID

Oral

3rd Generation

Cefdinir Some Trade Names
OMNICEF
Click for Drug Monograph

Oral

Cefditoren

Oral

Cefixime Some Trade Names
SUPRAX
Click for Drug Monograph

Oral

Cefoperazone

Parenteral

Cefotaxime Some Trade Names
CLAFORAN
Click for Drug Monograph

Parenteral

Cefpodoxime Some Trade Names
VANTIN
Click for Drug Monograph

Oral

Ceftazidime Some Trade Names
FORTAZ
TAZICEF
Click for Drug Monograph

Parenteral

Ceftibuten Some Trade Names
CEDAX
Click for Drug Monograph

Oral

Ceftizoxime Some Trade Names
CEFIZOX

Parenteral

Ceftriaxone Some Trade Names
ROCEPHIN
Click for Drug Monograph

Parenteral

4th Generation

Cefepime Some Trade Names
MAXIPIME
Click for Drug Monograph

Parenteral

5th Generation

Ceftobiprole

Parenteral

*Loracarbef Some Trade Names
LORABID

is technically a carbacephem, and cefoxitin Some Trade Names
MEFOXIN
Click for Drug Monograph
and cefotetan Some Trade Names
CEFOTAN
Click for Drug Monograph
are technically cephamycins, but they are grouped with cephalosporins because of similar antimicrobial spectra and pharmacology.

Pharmacology

Cephalosporins penetrate well into most body fluids and the ECF of most tissues, especially when inflammation (which enhances diffusion) is present. However, the only cephalosporins that reach CSF levels high enough to treat meningitis are

  • Ceftriaxone Some Trade Names
    ROCEPHIN
    Click for Drug Monograph
  • Cefotaxime Some Trade Names
    CLAFORAN
    Click for Drug Monograph
  • Ceftazidime Some Trade Names
    FORTAZ
    TAZICEF
    Click for Drug Monograph
  • Cefepime Some Trade Names
    MAXIPIME
    Click for Drug Monograph

All cephalosporins penetrate poorly into ICF and the vitreous humor.

Most cephalosporins are excreted primarily in urine, so their doses must be adjusted in patients with renal insufficiency. Cefoperazone and ceftriaxone Some Trade Names
ROCEPHIN
Click for Drug Monograph
, which have significant biliary excretion, do not require such dose adjustment.

Indications

Cephalosporins are bactericidal for most of the following:

  • Gram-positive bacteria
  • Gram-negative bacteria

Cephalosporins are classified in generations (see Table 8: Some Clinical Uses of 3rd- and 4th-Generation CephalosporinsTables). The 1st-generation drugs are effective mainly against gram-positive organisms. Higher generations generally have expanded spectra against aerobic gram-negative bacilli. The 5th-generation cephalosporin ceftobiprole, which is not yet available in the US, is active against methicillin-resistant Staphylococcus aureus. Cephalosporins have the following limitations:

  • Lack of activity against enterococci
  • Lack of activity against methicillin-resistant staphylococci (except for ceftobiprole)
  • Lack of activity against anaerobic gram-negative bacilli (except for cefotetan Some Trade Names
    CEFOTAN
    Click for Drug Monograph
    and cefoxitin Some Trade Names
    MEFOXIN
    Click for Drug Monograph
    )

First-generation cephalosporins:

These drugs have excellent activity against



  • Gram-positive cocci

Oral 1st-generation cephalosporins are commonly used for uncomplicated skin and soft-tissue infections, which are usually due to staphylococci and streptococci. Parenteral cefazolin Some Trade Names
ANCEF
KEFZOL
Click for Drug Monograph
is frequently used for endocarditis due to methicillin-sensitive S. aureus and for prophylaxis before cardiothoracic, orthopedic, abdominal, and pelvic surgery.



Second-generation cephalosporins and cephamycins:

Second-generation cephalosporins are active against



  • Gram-positive cocci
  • Certain gram-negative bacilli

Cephamycins are active against



  • Bacteroides sp, including B. fragilis

These drugs may be slightly less active against gram-positive cocci than 1st-generation cephalosporins. Second-generation cephalosporins and cephamycins are often used for polymicrobial infections that include gram-negative bacilli and gram-positive cocci. Because cephamycins are active against Bacteroides sp, they can be used when anaerobes are suspected (eg, in intra-abdominal sepsis, decubitus ulcers, and diabetic foot infections). However, in some medical centers, these bacilli are no longer reliably susceptible to cephamycins.



Third-generation cephalosporins:

These drugs are active against



  • Haemophilus influenzae and some Enterobacteriaceae (eg, Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis) that do not produce ampC β-lactamase or extended-spectrum β-lactamase (ESBL)

Ceftazidime Some Trade Names
FORTAZ
TAZICEF
Click for Drug Monograph
and cefoperazone are also active against



  • Pseudomonas aeruginosa

Some 3rd-generation cephalosporins have relatively poor activity against gram-positive cocci. Oral cefixime Some Trade Names
SUPRAX
Click for Drug Monograph
and ceftibuten Some Trade Names
CEDAX
Click for Drug Monograph
have little activity against S. aureus and, if used for skin and soft-tissue infections, should be restricted to uncomplicated infections due to streptococci. These cephalosporins have many clinical uses, as does the 4th-generation cephalosporin (see Table 8: Some Clinical Uses of 3rd- and 4th-Generation CephalosporinsTables).



Fourth-generation cephalosporin:

The 4th-generation cephalosporin cefepime Some Trade Names
MAXIPIME
Click for Drug Monograph
has activity against



  • Gram-positive cocci (similar to cefotaxime Some Trade Names
    CLAFORAN
    Click for Drug Monograph
    )
  • Gram-negative bacilli (enhanced activity), including P. aeruginosa (similar to ceftazidime Some Trade Names
    FORTAZ
    TAZICEF
    Click for Drug Monograph
    ), ESBL-producing K. pneumoniae and E. coli, and ampC β-lactamase–producing Enterobacteriaceae, such as Enterobacter sp

Table 8

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Some Clinical Uses of 3rd- and 4th-Generation Cephalosporins

Drug

Indications

Comments

3rd- and 4th-generation cephalosporins

Polymicrobial infections involving gram-negative bacilli and gram-positive cocci (eg, intra-abdominal sepsis, decubitus ulcers, diabetic foot infections)

When necessary, used with other drugs to cover anaerobes or enterococci

Ceftriaxone Some Trade Names
ROCEPHIN
Click for Drug Monograph
and some other 3rd-generation drugs

Community-acquired pneumonia

Used with a macrolide to cover atypical pathogens (mycoplasmas, Chlamydophila sp, Legionella sp)

Cefotaxime Some Trade Names
CLAFORAN
Click for Drug Monograph

Ceftriaxone Some Trade Names
ROCEPHIN
Click for Drug Monograph

Acute meningitis suspected to be due to Streptococcus pneumoniae, Haemophilus influenzae, or Neisseria meningitides

Used with ampicillin Some Trade Names
OMNIPEN
PRINCIPEN
Click for Drug Monograph
to cover Listeria monocytogenes and with vancomycin Some Trade Names
VANCOCIN
Click for Drug Monograph
to cover S. pneumoniae with reduced penicillin sensitivity (pending MIC results*)

Cefpodoxime Some Trade Names
VANTIN
Click for Drug Monograph
(oral)

Uncomplicated skin and soft-tissue infections due to staphylococci or streptococci

Not used if methicillin-resistant Staphylococcus aureus is suspected

Ceftazidime Some Trade Names
FORTAZ
TAZICEF
Click for Drug Monograph

Empiric therapy for postneurosurgical meningitis to cover Pseudomonas aeruginosa

Used with vancomycin Some Trade Names
VANCOCIN
Click for Drug Monograph
to cover methicillin-resistant S. aureus

Ceftriaxone Some Trade Names
ROCEPHIN
Click for Drug Monograph

Endocarditis caused by HACEK organisms

—

Endocarditis due to penicillin-sensitive streptococci

—

Lyme disease with neurologic complications (except isolated Bell's palsy), carditis, or arthritis

—

Uncomplicated gonococcal infections, chancroid, or both

Single IM dose

* Pneumococcal strains that are resistant to ceftriaxone Some Trade Names
ROCEPHIN
Click for Drug Monograph
and cefotaxime Some Trade Names
CLAFORAN
Click for Drug Monograph
have been reported, and guidelines suggest that if CSF strains have MICs of ≥ 1.0 μg/mL, they should be considered nonsusceptible to 3rd-generation cephalosporins.

HACEK = Haemophilus, Actinobacillus, Cardiobacterium, Eikenella, and Kingella spp; MICs = minimum inhibitory concentrations.

Fifth-generation cephalosporin:

The 5th-generation cephalosporin ceftobiprole is active against



  • Methicillin-resistant S. aureus

Contraindications

Cephalosporins are contraindicated in patients who are allergic to them or who have had an anaphylactic reaction to penicillins.

Use During Pregnancy and Breastfeeding

Cephalosporins are in pregnancy category B (animal studies show no risk and human evidence is incomplete, or animal studies show risk but human studies do not).

Cephalosporins enter breast milk and may alter bowel flora of the infant. Thus, use during breastfeeding is often discouraged.

Adverse Effects

Significant adverse effects include

  • Hypersensitivity reactions (most common)
  • Clostridium difficile–induced diarrhea (pseudomembranous colitis)
  • Leukopenia
  • Thrombocytopenia
  • Positive Coombs' test (although hemolytic anemia is very uncommon)

Hypersensitivity reactions are the most common systemic adverse effects; rash is common, but immediate IgE-mediated urticaria and anaphylaxis are rare.

Cross-sensitivity between cephalosporins and penicillins is uncommon; cephalosporins can be given cautiously to patients with a history of delayed hypersensitivity to penicillin if necessary. However, cephalosporins should not be used in patients who have had an anaphylactic reaction to penicillin. Pain at the IM injection site and thrombophlebitis after IV use may occur.

Cefamandole (no longer available in the US), cefoperazone, and cefotetan Some Trade Names
CEFOTAN
Click for Drug Monograph
may have a disulfiram Some Trade Names
ANTABUSE
Click for Drug Monograph
-like effect when ethanol is ingested, causing nausea and vomiting. Cefamandole, cefoperazone, and cefotetan Some Trade Names
CEFOTAN
Click for Drug Monograph
may elevate the PT/INR and PTT, an effect that is reversible with vitamin K.

Contraindications

Ceftriaxone Some Trade Names
ROCEPHIN
Click for Drug Monograph
is contraindicated as follows:

  • Ceftriaxone Some Trade Names
    ROCEPHIN
    Click for Drug Monograph
    IV must not be coadministered with Ca-containing IV solutions (including continuous Ca-containing infusions such as parenteral nutrition) in neonates ≤ 28 days because precipitation of ceftriaxone Some Trade Names
    ROCEPHIN
    Click for Drug Monograph
    -Ca salt is a risk. Fatal reactions with ceftriaxone Some Trade Names
    ROCEPHIN
    Click for Drug Monograph
    -Ca precipitates in the lungs and kidneys of neonates have been reported. In some cases, different infusion lines were used, and ceftriaxone Some Trade Names
    ROCEPHIN
    Click for Drug Monograph
    and Ca-containing solutions were given at different times. To date, no intravascular or pulmonary precipitates have been reported in patients other than neonates who are treated with ceftriaxone Some Trade Names
    ROCEPHIN
    Click for Drug Monograph
    and Ca-containing IV solutions. However, because an interaction between ceftriaxone Some Trade Names
    ROCEPHIN
    Click for Drug Monograph
    and IV Ca-containing solutions is theoretically possible in patients other than neonates, ceftriaxone Some Trade Names
    ROCEPHIN
    Click for Drug Monograph
    and Ca-containing solutions should not be mixed or given within 48 h of each other (based on 5 half-lives of ceftriaxone Some Trade Names
    ROCEPHIN
    Click for Drug Monograph
    )—even via different infusion lines at different sites—to any patient regardless of age. No data on potential interaction between ceftriaxone Some Trade Names
    ROCEPHIN
    Click for Drug Monograph
    and oral Ca-containing products or on interaction between IM ceftriaxone Some Trade Names
    ROCEPHIN
    Click for Drug Monograph
    and Ca-containing products (IV or oral) are available.
  • Ceftriaxone Some Trade Names
    ROCEPHIN
    Click for Drug Monograph
    should not be given to hyperbilirubinemic and preterm neonates because in vitro, ceftriaxone Some Trade Names
    ROCEPHIN
    Click for Drug Monograph
    can displace bilirubin from serum albumin, potentially triggering kernicterus.

Penicillins

Penicillins (Table 9: PenicillinsTables) are bactericidal by unknown mechanisms but perhaps by activating autolytic enzymes that destroy the cell wall in some bacteria. Some bacteria produce β-lactamase, which inactivates the drug; this effect can be blocked by adding a β-lactamase inhibitor (clavulanate, sulbactam, or tazobactam). However, available β-lactamase inhibitors do not inhibit ampC β-lactamases, commonly produced by Enterobacter, Serratia, Citrobacter, Providencia, and Morganella spp or by P. aeruginosa, and these drugs may only partially inhibit ESBL produced by some K. pneumoniae, E. coli, and other Enterobacteriaceae.

Table 9

PrintOpen table Open table in new window
Penicillins

Drug

Route

Penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
–like drugs

Penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph

Oral or parenteral

Penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
benzathine

Parenteral

Penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
procaine

Parenteral

Penicillin V

Oral

Ampicillin Some Trade Names
OMNIPEN
PRINCIPEN
Click for Drug Monograph
-like drugs

Ampicillin Some Trade Names
OMNIPEN
PRINCIPEN
Click for Drug Monograph

Oral or parenteral

Ampicillin Some Trade Names
OMNIPEN
PRINCIPEN
Click for Drug Monograph
plus sulbactam

Parenteral

Amoxicillin Some Trade Names
AMOXIL
TRIMOX
Click for Drug Monograph

Oral

Amoxicillin Some Trade Names
AMOXIL
TRIMOX
Click for Drug Monograph
plus clavulanate

Oral

Penicillinase-resistant penicillins

Dicloxacillin Some Trade Names
DYCILL
DYNAPEN
PATHOCIL
Click for Drug Monograph

Oral

Nafcillin Some Trade Names
UNIPEN
Click for Drug Monograph

Oral or parenteral

Oxacillin Some Trade Names
BACTOCILL
PROSTAPHLIN
Click for Drug Monograph

Oral or parenteral

Broad-spectrum (antipseudomonal) penicillins

Carbenicillin Some Trade Names
GEOCILLIN

Oral

Piperacillin Some Trade Names
PIPRACIL
Click for Drug Monograph

Parenteral

Piperacillin Some Trade Names
PIPRACIL
Click for Drug Monograph
plus tazobactam

Parenteral

Ticarcillin Some Trade Names
TICAR

Parenteral

Ticarcillin Some Trade Names
TICAR

plus clavulanate

Parenteral

Penicillins

Drug

Route

Penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
–like drugs

Penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph

Oral or parenteral

Penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
benzathine

Parenteral

Penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
procaine

Parenteral

Penicillin V

Oral

Ampicillin Some Trade Names
OMNIPEN
PRINCIPEN
Click for Drug Monograph
-like drugs

Ampicillin Some Trade Names
OMNIPEN
PRINCIPEN
Click for Drug Monograph

Oral or parenteral

Ampicillin Some Trade Names
OMNIPEN
PRINCIPEN
Click for Drug Monograph
plus sulbactam

Parenteral

Amoxicillin Some Trade Names
AMOXIL
TRIMOX
Click for Drug Monograph

Oral

Amoxicillin Some Trade Names
AMOXIL
TRIMOX
Click for Drug Monograph
plus clavulanate

Oral

Penicillinase-resistant penicillins

Dicloxacillin Some Trade Names
DYCILL
DYNAPEN
PATHOCIL
Click for Drug Monograph

Oral

Nafcillin Some Trade Names
UNIPEN
Click for Drug Monograph

Oral or parenteral

Oxacillin Some Trade Names
BACTOCILL
PROSTAPHLIN
Click for Drug Monograph

Oral or parenteral

Broad-spectrum (antipseudomonal) penicillins

Carbenicillin Some Trade Names
GEOCILLIN

Oral

Piperacillin Some Trade Names
PIPRACIL
Click for Drug Monograph

Parenteral

Piperacillin Some Trade Names
PIPRACIL
Click for Drug Monograph
plus tazobactam

Parenteral

Ticarcillin Some Trade Names
TICAR

Parenteral

Ticarcillin Some Trade Names
TICAR

plus clavulanate

Parenteral

Pharmacology

Food does not interfere with absorption of amoxicillin Some Trade Names
AMOXIL
TRIMOX
Click for Drug Monograph
, but penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
should be given 1 h before or 2 h after a meal. Amoxicillin Some Trade Names
AMOXIL
TRIMOX
Click for Drug Monograph
has generally replaced ampicillin Some Trade Names
OMNIPEN
PRINCIPEN
Click for Drug Monograph
for oral use because amoxicillin Some Trade Names
AMOXIL
TRIMOX
Click for Drug Monograph
is absorbed better, has fewer GI effects, and can be given less frequently.

Penicillins are distributed rapidly in the ECF of most tissues, particularly when inflammation is present.

All penicillins except nafcillin Some Trade Names
UNIPEN
Click for Drug Monograph
are excreted in urine and reach high levels in urine. Parenteral penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
is rapidly excreted (serum half-life 0.5 h), except for repository forms (the benzathine or procaine salt of penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
); these forms are intended for deep IM injection only and provide a tissue depot from which absorption takes place over several hours to several days. Benzathine penicillin reaches its peak level more slowly and is generally longer-acting than procaine penicillin.

Indications

Penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
–like drugs (including penicillin V) are primarily used against

  • Gram-positive bacteria
  • Some gram-negative cocci (eg, meningococci)

A minority of gram-negative bacilli are also susceptible to large parenteral doses of penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
. Most staphylococci, most Neisseria gonorrhoeae, many anaerobic gram-negative bacilli, and about 30% of H. influenzae are resistant. Penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
is the drug of choice for syphilis and, with gentamicin Some Trade Names
GARAMYCIN
Click for Drug Monograph
, for endocarditis due to susceptible enterococci.

Benzathine penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
is available as pure benzathine penicillin, a mixture of equal amounts of benzathine and procaine penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
, and a mixture of 0.9 million units benzathine and 0.3 million units procaine penicillin G Some Trade Names
BICILLIN
WYCILLIN
Click for Drug Monograph
. Of the 3 products, only pure benzathine penicillin is recommended for treating syphilis and preventing rheumatic fever. Whether the mixture of equal amounts is effective in treating syphilis is unknown. Pure benzathine penicillin and the mixture of equal amounts are indicated for treating URIs and skin and soft-tissue infections caused by susceptible streptococci.

Amoxicillin and ampicillin:

These drugs are more active against



  • Enterococci
  • Certain gram-negative bacilli, such as non-β-lactamase–producing H. influenzae, E. coli, and P. mirabilis; Salmonella sp; and Shigella sp

The addition of a β-lactamase inhibitor allows use against methicillin-sensitive staphylococci, H. influenzae, N. gonorrhoeae, Moraxella catarrhalis, Bacteroides sp, E. coli, and K. pneumoniae. Ampicillin Some Trade Names
OMNIPEN
PRINCIPEN
Click for Drug Monograph
is indicated primarily for infections typically caused by susceptible gram-negative bacteria:



  • UTIs
  • Meningococcal meningitis
  • Biliary sepsis
  • Respiratory infections
  • Listeria meningitis
  • Enterococcal infections
  • Some typhoid fever and typhoid carriers

Penicillinase-resistant penicillins:

These drugs are used primarily for



  • Penicillinase-producing methicillin-sensitive S. aureus

These drugs are also used to treat some S. pneumoniae, group A streptococcal, and methicillin-sensitive coagulase-negative staphylococcal infections.



Broad-spectrum (antipseudomonal) penicillin:

These drugs have activity against



  • Bacteria susceptible to ampicillin Some Trade Names
    OMNIPEN
    PRINCIPEN
    Click for Drug Monograph
  • Some strains of Enterobacter and Serratia spp
  • Many strains of P. aeruginosa

Ticarcillin Some Trade Names
TICAR

is less active against enterococci than piperacillin Some Trade Names
PIPRACIL
Click for Drug Monograph
. The addition of a β-lactamase inhibitor enhances activity against β-lactamase–producing methicillin-sensitive S. aureus, E. coli, K. pneumoniae, H. influenzae, and gram-negative anaerobic bacilli, but not against gram-negative bacilli that produce ampC β-lactamase, and may only partially inhibit ESBL produced by some K. pneumoniae, E. coli, and other Enterobacteriaceae. Broad-spectrum penicillins exhibit synergy with aminoglycosides and are usually used with this class to treat P. aeruginosa infections.



Contraindications

Penicillins are contraindicated in patients who have had serious allergic reactions to them.

Use During Pregnancy and Breastfeeding

Penicillins are in pregnancy category B (animal studies show no risk and human evidence is incomplete, or animal studies show risk but human studies do not).

Penicillins enter breast milk in small amounts. Their use is usually considered compatible with breastfeeding.

Adverse Effects

Adverse effects include

  • Hypersensitivity reactions, including rashes (most common)

Other adverse effects occur less commonly.

Hypersensitivity:

Most adverse effects are hypersensitivity reactions:



  • Immediate reactions: Anaphylaxis (which can cause death within minutes), urticaria and angioneurotic edema (in 1 to 5/10,000 injections), and death (in about 0.3/10,000 injections)
  • Delayed reactions (in up to 8% of patients): Serum sickness, rashes (eg, macular, papular, morbilliform), and exfoliative dermatitis (which usually appears after 7 to 10 days of therapy)

Most patients who report an allergic reaction to penicillin do not react to subsequent exposure to penicillin. Although small, risk of an allergic reaction is about 10 times higher for patients who have had a previous allergic reaction. Many patients report adverse reactions to penicillin that are not truly allergic (eg, GI adverse effects, nonspecific symptoms). If patients have a vague or inconsistent history of penicillin allergy and taking alternative antibiotics is not effective or convenient, skin testing may be done (see Skin testing). Desensitization may be attempted in patients with a positive skin test if there is no alternative to a penicillin-type drug. However, patients with a history of anaphylaxis to penicillin should not be given any β-lactam again (including for skin testing), except in very rare circumstances when no substitute can be found. In such cases, special precautions and desensitization regimens are required (see Desensitization).



Rashes:

Rashes occur more often with ampicillin Some Trade Names
OMNIPEN
PRINCIPEN
Click for Drug Monograph
and amoxicillin Some Trade Names
AMOXIL
TRIMOX
Click for Drug Monograph
than with other penicillins. Patients with infectious mononucleosis often develop a nonallergic rash, typically maculopapular, usually beginning between days 4 and 7 of treatment.



Other adverse effects:

Penicillins can also cause



  • CNS toxicity (eg, seizures) if doses are high, especially in patients with renal insufficiency
  • Nephritis
  • C. difficile–induced diarrhea (pseudomembranous colitis)
  • Coombs'-positive hemolytic anemia
  • Leukopenia
  • Thrombocytopenia

Leukopenia seems to occur most often with nafcillin Some Trade Names
UNIPEN
Click for Drug Monograph
. Any penicillin used in very high IV doses can interfere with platelet function and cause bleeding, but ticarcillin Some Trade Names
TICAR

is the most common cause, especially in patients with renal insufficiency.



Other adverse effects include pain at the IM injection site, thrombophlebitis when the same site is used repeatedly for IV injection, and, with oral formulations, GI disturbances. Rarely, black tongue, due to irritation of the glossal surface and keratinization of the superficial layers, occurs, usually when oral formulations are used. Ticarcillin Some Trade Names
TICAR

in high doses may cause Na overload because ticarcillin Some Trade Names
TICAR

is a disodium salt. Ticarcillin Some Trade Names
TICAR

can also cause hypokalemic metabolic alkalosis because the large amount of nonabsorbable anion presented to the distal tubules alters H+ ion excretion and secondarily results in K+ loss.



Dosing Considerations

Because penicillins, except nafcillin Some Trade Names
UNIPEN
Click for Drug Monograph
, reach high levels in urine, doses must be reduced in patients with severe renal insufficiency. Probenecid Some Trade Names
No US trade name
Click for Drug Monograph
inhibits renal tubular secretion of many penicillins, increasing blood levels. It is sometimes given to maintain high blood levels.

Other β-Lactams

Carbapenems (imipenem, meropenem Some Trade Names
MERREM
Click for Drug Monograph
, doripenem, and ertapenem Some Trade Names
INVANZ
Click for Drug Monograph
) are parenteral bactericidal antibiotics that have an extremely broad spectrum. They are active against

  • H. influenzae
  • Anaerobes
  • Most Enterobacteriaceae (including those that produce ampC β-lactamase and ESBL, although P. mirabilis tends to have higher imipenem MICs)
  • Methicillin-sensitive staphylococci and streptococci, including S. pneumoniae (except possibly strains with reduced penicillin sensitivity)

Most Enterococcus faecalis and many P. aeruginosa strains, including those resistant to broad-spectrum penicillins and cephalosporins, are susceptible to imipenem, meropenem Some Trade Names
MERREM
Click for Drug Monograph
, and doripenem but are resistant to ertapenem Some Trade Names
INVANZ
Click for Drug Monograph
. Carbapenems are active synergistically with aminoglycosides against P. aeruginosa. E. faecium and methicillin-resistant staphylococci are resistant.

Many multidrug-resistant hospital-acquired bacteria are sensitive only to carbapenems. However, expanded use of carbapenems has resulted in some carbapenem resistance.

Imipenem and meropenem Some Trade Names
MERREM
Click for Drug Monograph
penetrate into CSF when meninges are inflamed. Meropenem Some Trade Names
MERREM
Click for Drug Monograph
is used for gram-negative bacillary meningitis; imipenem is not used in meningitis because it may cause seizures. Most seizures occur in patients who have CNS abnormalities or renal insufficiency and who are given inappropriately high doses.

Aztreonam is a parenteral bactericidal antibiotic; it is as active as ceftazidime Some Trade Names
FORTAZ
TAZICEF
Click for Drug Monograph
against

  • Enterobacteriaceae that do not produce ampC β-lactamase or ESBL
  • P. aeruginosa

Aztreonam Some Trade Names
AZACTAM
Click for Drug Monograph
is not active against anaerobes. Gram-positive bacteria are resistant to aztreonam Some Trade Names
AZACTAM
Click for Drug Monograph
(in contrast to cephalosporins). Aztreonam Some Trade Names
AZACTAM
Click for Drug Monograph
acts synergistically with aminoglycosides. Because the metabolic products of aztreonam Some Trade Names
AZACTAM
Click for Drug Monograph
differ from those of other β-lactams, cross-hypersensitivity is unlikely. Thus, aztreonam Some Trade Names
AZACTAM
Click for Drug Monograph
is used mainly for

  • Severe aerobic gram-negative bacillary infections, including meningitis, in patients who have a serious β-lactam allergy but who nevertheless require β-lactam therapy

Other antibiotics are added to cover any suspected gram-positive cocci and anaerobes. The dose is reduced in renal failure.

Last full review/revision July 2009 by Matthew E. Levison, MD

Content last modified August 2013

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In This Topic
Infectious Diseases
Bacteria and Antibacterial Drugs
β-Lactams
Cephalosporins
Pharmacology
Indications
First-generation cephalosporins
Second-generation cephalosporins and cephamycins
Third-generation cephalosporins
Fourth-generation cephalosporin
Fifth-generation cephalosporin
Contraindications
Use During Pregnancy and Breastfeeding
Adverse Effects
Contraindications
Penicillins
Pharmacology
Indications
Amoxicillin and ampicillin
Penicillinase-resistant penicillins
Broad-spectrum (antipseudomonal) penicillin
Contraindications
Use During Pregnancy and Breastfeeding
Adverse Effects
Hypersensitivity
Rashes
Other adverse effects
Dosing Considerations
Other β-Lactams
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