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78 PART 2 Antibacterial Drugs<br />

association with Clostridium difficile–associated<br />

diarrhea. Cefpodoxime has the MTT side chain<br />

that can inhibit vitamin K production (see section<br />

on second-generation cephalosporins for details).<br />

■■<br />

Important Facts<br />

• Ceftazidime is the exception to the spectrum<br />

of activity rule for third-generation agents.<br />

Unlike the others, it is antipseudomonal and<br />

lacks clinically useful activity against Grampositive<br />

organisms.<br />

• Ceftriaxone, cefotaxime, and ceftazidime cross<br />

the blood–brain barrier effectively and are<br />

useful for the treatment of CNS infections.<br />

However, their differences in activity lead clinicians<br />

to use them for different types of infections.<br />

Ceftazidime would be a poor choice for<br />

community-acquired meningitis, in which<br />

Streptococcus pneumoniae predominates.<br />

• Third-generation cephalosporins are notorious<br />

for inducing resistance among GNRs. Though<br />

they can be useful in nosocomial infections, too<br />

much broad-spectrum utilization can result in<br />

harder-to-treat organisms.<br />

• A one-time dose of ceftriaxone 125 mg IM has<br />

been a drug-of-choice for gonorrhea for many<br />

years, but the dose was recently increased<br />

to 250 mg IM due to increasing resistance.<br />

Patients treated for gonorrhea should receive<br />

empiric therapy for chlamydia as well, which<br />

ceftriaxone does not work against.<br />

• Ceftriaxone has the characteristic of having<br />

dual modes of elimination via both renal and

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