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134 PART 2 Antibacterial Drugs<br />

Spectrum<br />

Good: Staphylococcus aureus (including many<br />

MRSA strains), Haemophilus influenzae, Stenotrophomonas<br />

maltophilia, Listeria, Pneumocystis<br />

jirovecii (formerly known as P. carinii), Toxoplasma<br />

gondii (pyrimethamine and sulfadiazine)<br />

Moderate: enteric GNRs, S. pneumoniae, Salmonella,<br />

Shigella, Nocardia<br />

Poor: Pseudomonas, enterococci, S. pyogenes,<br />

anaerobes<br />

Adverse Effects<br />

Dermatologic: TMP/SMX frequently causes rash,<br />

usually because of the sulfamethoxazole component.<br />

Rash is much more common in HIV/<br />

AIDS patients. Although these rashes are usually<br />

not severe, life-threatening dermatologic<br />

reactions such as toxic epidermal necrolysis<br />

and Stevens-Johnson syndrome have been<br />

documented.<br />

Hematologic: A primarily dose-dependent bonemarrow<br />

suppression can be seen with TMP/<br />

SMX, especially at the higher doses used to<br />

treat Pneumocystis infections.<br />

Renal: Confusingly, TMP/SMX can cause both true<br />

and pseudo-renal failure. Crystalluria and AIN<br />

caused by the SMX component can lead to acute<br />

renal failure; however, the blockade of creatinine<br />

secretion by TMP can cause an increase<br />

in serum creatinine without a true decline<br />

in glomerular filtration rate. TMP can also<br />

cause hyperkalemia in a fashion similar to the<br />

potassium-sparing diuretics (e.g., triamterene).

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