What are the considerations for using alverine (antispasmodic) and simethicone (antifoaming agent) in patients with Chronic Kidney Disease (CKD)?

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Last updated: February 4, 2026View editorial policy

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Alverine and Simethicone Use in Chronic Kidney Disease

Alverine citrate and simethicone can be used safely in patients with CKD without dose adjustment, as neither drug undergoes significant renal elimination.

Pharmacokinetic Considerations

Both alverine and simethicone have favorable pharmacokinetic profiles in CKD:

  • Simethicone is not systemically absorbed and acts locally in the gastrointestinal tract as an antifoaming agent, making renal function irrelevant to its safety profile 1, 2

  • Alverine citrate undergoes primarily hepatic metabolism rather than renal elimination, so accumulation in CKD is not expected 1, 3

  • Neither medication appears on lists of drugs requiring dose adjustment or avoidance in renal impairment 1, 2, 4

Clinical Efficacy and Safety

The combination has demonstrated efficacy for IBS-related symptoms:

  • Alverine citrate 60 mg with simethicone 300 mg three times daily significantly reduced abdominal pain/discomfort compared to placebo (median VAS score 40 mm vs 50 mm, p=0.047) in a randomized controlled trial 5

  • The responder rate was significantly higher with active treatment (46.8% vs 34.3%, p=0.01) 5

  • Adverse events were similar between treatment and placebo groups, suggesting good tolerability 5

Practical Prescribing Approach

Standard dosing can be used across all CKD stages:

  • Use the standard dose of alverine citrate 60 mg with simethicone 300 mg three times daily regardless of eGFR 5

  • No monitoring of renal function is required specifically for these medications 1, 3

  • Consider the overall medication burden in CKD patients, as polypharmacy is associated with increased hospitalization and mortality risk 6

Important Caveats

Focus on evidence-based CKD therapies first:

  • Ensure optimization of disease-modifying therapies (SGLT2 inhibitors, RAS inhibitors) before adding symptomatic treatments 7

  • Avoid polypharmacy without clear benefit, as CKD patients average 8-9 medications daily with associated risks 6

  • Medication reconciliation is critical during transitions of care to prevent inappropriate prescriptions 6

References

Research

Drug dosing in chronic kidney disease.

The Medical clinics of North America, 2005

Research

Drug use and dosing in chronic kidney disease.

Annals of the Academy of Medicine, Singapore, 2009

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Evidence-Based Management of Chronic Kidney Disease

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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