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154 PART 3 Antimycobacterial Drugs<br />

Spectrum<br />

Good: most mycobacteria<br />

Moderate: Staphylococcus, Acinetobacter, Enterobacteriaceae<br />

Poor: “typical” bacteria as monotherapy, some<br />

very rare mycobacteria<br />

Adverse Effects<br />

Rifamycins are generally well-tolerated drugs<br />

that are most notorious for their potent CYP450-<br />

inducing effects. Their potent induction of metabolism<br />

can lead to subtherapeutic concentrations of<br />

other drugs that can manifest with devastating<br />

clinical consequences, such as loss of seizure control<br />

(anticonvulsants) or organ rejection (antirejection<br />

agents). Rifampin characteristically colors<br />

secretions (urine, tears, etc.) orange-red and can<br />

actually stain contact lenses, which should not<br />

be worn during rifampin therapy. Otherwise, this<br />

effect is nonpermanent and not harmful, which<br />

patients appreciate knowing. Rifamycins can also<br />

cause hepatotoxicity. Less serious side effects<br />

include rash, nausea, vomiting, and hypersensitivity<br />

(often fever).<br />

■■<br />

Important Facts<br />

• Rifampin is a drug of choice for tuberculosis,<br />

while rifabutin is a drug of choice for MAC,<br />

although both drugs have activity against both<br />

pathogens. MAC infections are most common<br />

in patients with HIV, who are often taking<br />

antiretroviral therapy that is metabolized by<br />

CYP450. Because rifabutin has somewhat lesspotent<br />

CYP450-inducing effects than rifampin,

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