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42 PART 1 Antibiotic Therapy<br />

cross-reactivity are available for beta-lactam drugs,<br />

estimates for cross-reactivity within other classes<br />

(for example, between fluoroquinolones) are essentially<br />

nonexistent. Because labeling a patient with<br />

an allergy to a particular antibiotic can limit future<br />

treatment options severely and possibly lead to<br />

the selection of inferior drugs, every effort should<br />

be made to clarify the exact nature of a reported<br />

allergy.<br />

Antibiotic Toxicities<br />

Despite being designed to affect the physiology of<br />

microorganisms rather than humans, antibiotics<br />

can have direct toxic effects on patients. In some<br />

cases, this is an extension of their mechanism of<br />

action when selectivity for microorganisms is not<br />

perfect. For example, the hematologic adverse<br />

effects of trimethoprim stem from its inhibition<br />

of folate metabolism in humans, which is also<br />

its mechanism of antibiotic effect. In other cases,<br />

antibiotics display toxicity through unintended<br />

physiologic interactions, such as when vancomycin<br />

stimulates histamine release, leading to its characteristic<br />

red man syndrome. Some of these toxicities<br />

may be dose related and toxicity often occurs when<br />

doses are not adjusted properly for renal dysfunction<br />

and thus accumulate to a toxic level. Proper<br />

dosage adjustment can reduce the risk of doserelated<br />

toxicities.<br />

Superinfection<br />

The human body is colonized by a variety of<br />

bacteria and fungi. These organisms are generally<br />

considered commensals, in that they benefit

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