BIAXIN
Pronunciation: kla-RITH-roe-mye-sin


What it isMacrolide inhibiting the bacterial 50S subunit; respiratory and mycobacterial infections.
Why this oneIts Gram-positive activity and role in Helicobacter pylori regimens distinguish it from azithromycin.
What limits it⚑ It strongly inhibits CYP3A4—colchicine can become fatal in renal impairment. QT prolongation adds another interaction hazard.
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| FDA dosing | Population | Start | Target | Max |
|---|---|---|---|---|
| Respiratory/skin infections (bronchitis, sinusitis, pneumonia, pharyngitis, skin) | Adults | 250–500 mg BID | 250–500 mg every 12 h × 7–14 days | |
| Acute otitis media / pediatric infections | Pediatric | 15 mg/kg/day divided BID | 15 mg/kg/day divided every 12 h × 10 days | Up to adult dose |
| Disseminated MAC (treatment/prophylaxis) | Adults & pediatric | 500 mg BID (adults) | 500 mg every 12 h (adults); 7.5 mg/kg every 12 h (pediatric) | 500 mg BID (pediatric) |
| H. pylori eradication / duodenal ulcer (combination therapy) | Adults | 500 mg every 8–12 h | 500 mg every 8–12 h × 10–14 days with a PPI ± amoxicillin |
Renal Severe (CrCl <30 mL/min): reduce dose 50%. With atazanavir/ritonavir: reduce 50% (moderate) or 75% (severe).
Hepatic No adjustment needed in hepatic impairment with normal renal function.
Available strengths
Pregnancy Not recommended in pregnancy except when no alternative therapy is appropriate; animal malformations at clinically relevant doses.
Lactation Undefined.
Generic entry2004
NO BOXED WARNINGS
Principal riskA strong CYP3A4 inhibitor; QT prolongation
Legacy pregnancy categoryC
Defining liabilityStrong CYP3A inhibition and QT prolongation create major interaction risk.
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