TABLE 5.
Antimicrobial agents for treatment and postexposure prophylaxis for B. pertussis infection, 1997 to 2013a
Agent (reference[s]) | Age group | Dosing information | Comments |
---|---|---|---|
Erythromycin (220, 278, 332, 336, 344–346, 663) | >1 mo | 40–60 mg/kg/day in 3 or 4 divided doses for 7–14 days | Drug-drug interaction with those metabolized by cytochrome P450; poorly tolerated (e.g., GI upset, hypersensitivity reactions, cholestatic hepatitis, sensorineural hearing loss) |
Adults | 500 mg every 6 or 8 h for 7–14 days | Increased risk of IHPS in neonates; FDA pregnancy category B drug | |
Azithromycin (220, 278, 332, 336, 337) | <6 mo | 10 mg/kg daily for 5 days | Well tolerated but GI upset can still occur; Drug-drug interaction with those metabolized by cytochrome P450 |
≥6 mo | 10 mg/kg on day 1, followed by 5 mg/kg on days 2–5 | Administer 1 h before or 2 h after food and antacids | |
Adults | 500 mg on day 1, followed by 250 mg on days 2–5 | FDA pregnancy category B drug | |
Clarithromycin (220, 278, 332, 337) | >1 mo | 15 mg/kg/day in 2 divided doses for 7 days | Moderately tolerated (GI upset is common) |
Adults | 500 mg every 12 h for 7 days | Drug-drug interaction with those metabolized by cytochrome P450; FDA pregnancy category C drug | |
TMP-SMZ (278) | >2 mo | TMP at 8 mg/kg/day plus SMZ at 40 mg/kg/day every 12 h for 14 days | Second-line treatment for those who have macrolide resistance or intolerance; FDA pregnancy category C drug |
Adults | TMP at 320 mg/day plus SMZ at 1,600 mg/day every 12 h for 14 days | Contraindicated in pregnant women and breastfeeding mothers |
GI, gastrointestinal; FDA, Food and Drug Administration; IHPS, infantile hypertrophic pyloric stenosis; TMP-SMZ, trimethoprim-sulfamethoxazole (co-trimoxazole).