Can Rifaximin induce abdominal pain and leukocytosis?

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Last updated: September 14, 2025View editorial policy

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Rifaximin's Effects on Abdominal Pain and Leukocytosis

Rifaximin can cause abdominal pain but is unlikely to induce leukocytosis based on available evidence, with its safety profile being comparable to placebo in clinical trials. 1

Rifaximin and Abdominal Pain

Evidence on Abdominal Pain

  • Rifaximin has limited effects on abdominal pain in IBS-D patients according to the British Society of Gastroenterology guidelines 1
  • Meta-analyses show rifaximin is not efficacious for global symptoms or abdominal pain in IBS-D, though it improves stool consistency 1
  • In some cases, rifaximin may actually be used to treat abdominal pain in IBS-D patients, with one study showing:
    • 56.8% of patients had abdominal pain response (≥30% improvement) to open-label rifaximin 2
    • Weekly decreases in mean abdominal pain scores ranged from -2.6 to -3.3 points (on a 0-10 scale) 2

Common Side Effects

  • Headache is the most common adverse event reported with rifaximin, not abdominal pain 1
  • In clinical trials for IBS-D and hepatic encephalopathy, rifaximin's safety profile was comparable to placebo 3
  • Most common adverse effects in IBS trials included:
    • Abdominal pain (occurring in <10% of patients)
    • Diarrhea
    • Bad taste
    • Headache
    • Upper respiratory tract infection 3

Rifaximin and Leukocytosis

Evidence on Leukocytosis

  • There is no substantial evidence that rifaximin causes leukocytosis in the available literature
  • In fact, one study in patients with mild acute diverticulitis showed that rifaximin treatment resulted in a "marked significant reduction" of leukocytosis compared to baseline data (P < 0.01) 4
  • This suggests rifaximin may actually help reduce leukocytosis in certain inflammatory conditions rather than induce it

Clinical Applications and Safety Profile

Approved Indications

  • Rifaximin is FDA-approved for:
    • IBS with diarrhea (550 mg three times daily for 14 days) 5
    • Hepatic encephalopathy (550 mg twice daily) 5
    • Travelers' diarrhea (200 mg three times daily for 3 days) 5

Safety Considerations

  • Side effects are generally no more common with rifaximin than with placebo 1
  • Despite initial concerns, repeated courses of rifaximin have not shown increased risk of:
    • Clostridium difficile infection
    • Bacterial resistance 1, 5
  • In hepatic encephalopathy trials, common adverse events (10-15% of patients) included:
    • Ascites
    • Dizziness
    • Fatigue
    • Peripheral edema 3

Clinical Implications

Monitoring Recommendations

  • When prescribing rifaximin, monitor for:
    • Common side effects like headache
    • Improvement in target symptoms (e.g., stool consistency)
    • No specific monitoring for leukocytosis is indicated based on current evidence

Treatment Considerations

  • Rifaximin is considered a second-line drug for IBS-D in secondary care 1
  • Its effect on abdominal pain is limited compared to its effect on stool consistency 1
  • For patients reporting abdominal pain while on rifaximin, consider:
    • Evaluating for other causes of pain
    • Assessing if pain is related to the underlying condition rather than medication
    • Potentially adding targeted pain management if needed

In conclusion, while rifaximin may cause abdominal pain in some patients, this is relatively uncommon (<10%) and comparable to placebo rates. There is no evidence supporting rifaximin as a cause of leukocytosis; in fact, it may help reduce leukocytosis in certain inflammatory conditions.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Hepatic Encephalopathy Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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