rifaximin

Brand: Xifaxan

Prototype Drug
Drug Class: antibiotic (GI-specific)
Drug Family: antibiotic
Subclass: non-absorbed rifamycin antibiotic
Organ Systems: gastrointestinalinfectious-disease

Mechanism of Action

Rifamycin-class antibiotic with >99% local GI activity (minimal systemic absorption); inhibits bacterial RNA polymerase; primarily active against gram-positive and gram-negative enteric organisms.

bacterial RNA polymerase (beta subunit)

Indications

  • traveler's diarrhea (non-invasive E. coli)
  • hepatic encephalopathy prevention (secondary)
  • IBS-diarrhea predominant (IBS-D)

Contraindications

  • traveler's diarrhea with fever/bloody diarrhea (invasive pathogens)
  • severe hepatic impairment

Adverse Effects

Common

  • flatulence
  • headache
  • nausea

Serious

  • peripheral edema (rare in HE use)
  • Clostridium difficile (rare — low risk given non-systemic)

Pharmacokinetics (ADME)

Absorption <1% systemic absorption
Distribution GI lumen
Metabolism GI local, minimal systemic CYP3A4
Excretion fecal
Half-life not applicable — GI local
Onset 1-4 hours (luminal)
Peak 1-4 hours
Duration 8-12 hours
Protein Binding minimally
Vd minimal

Nursing Considerations

  1. For HE prevention: 550 mg BID ongoing after first HE episode
  2. No systemic drug interactions (negligible absorption)
  3. Take with or without food
  4. RIFAXIMIN-alpha for IBS-D: 550 mg TID x14 days

Clinical Pearls

  • PREVENT trial: rifaximin reduces overt hepatic encephalopathy recurrence by 58% vs placebo
  • Minimal systemic absorption: safe profile, no significant drug interactions

Safety Profile

Pregnancy use-with-caution
Lactation use-with-caution
Renal Adjustment Not required
Hepatic Adjustment Required
TDM Not required
Guideline Update pending

Concordance Terms

Cross-referenced clinical concepts — click any term to see all content where it appears.