Are there any interactions between cinnamon and medications like warfarin or midazolam?

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Last updated: September 9, 2025View editorial policy

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Cinnamon Interactions with Medications

Cinnamon can significantly interact with warfarin by inhibiting CYP2C9 enzyme and potentially with midazolam through CYP3A4 inhibition, requiring careful monitoring and possible dose adjustments of these medications.

Interaction with Warfarin

Cinnamon has documented interactions with warfarin that can increase the risk of bleeding complications:

  • Cinnamon inhibits CYP2C9, which is the primary enzyme responsible for metabolizing S-warfarin (the more potent isomer) 1
  • This inhibition can lead to increased warfarin levels and elevated INR values
  • According to the American Heart Association guidelines, herbs that inhibit CYP enzymes can significantly affect warfarin metabolism 1

Clinical Significance and Monitoring

  • The FDA warfarin label specifically lists botanical medicines as potential interaction risks, with some herbs increasing warfarin's effects 2
  • For patients taking both warfarin and cinnamon:
    • More frequent INR monitoring is recommended, especially when starting or stopping cinnamon consumption
    • Initial INR check should be performed at day 2-3 and follow-up at day 5-7
    • No preemptive warfarin dose reduction is recommended, but dose adjustments may be needed based on INR results

Interaction with Midazolam

Cinnamon may also interact with midazolam through inhibition of CYP3A4:

  • Cinnamon contains compounds that inhibit CYP3A4 1
  • Midazolam is primarily metabolized by CYP3A4, making it susceptible to this interaction
  • This interaction could potentially increase midazolam levels and enhance its sedative effects

Management Recommendations for Midazolam

  • Consider alternative sedatives if possible when patients are consuming significant amounts of cinnamon
  • If midazolam must be used, start with lower doses and titrate carefully
  • Monitor patients more closely for signs of excessive sedation

Quantity and Duration Considerations

The risk of clinically significant interactions appears to be dose-dependent:

  • Regular culinary use of cinnamon (small amounts in food) likely poses minimal risk
  • Higher doses (such as those in supplements) or prolonged use increase interaction potential
  • According to studies on herbal interactions, consuming large quantities of herbal products for extended periods (>3-4 weeks) significantly increases the risk of interactions 3

Practical Recommendations

  1. For patients on warfarin:

    • Document cinnamon consumption (amount and frequency)
    • Monitor INR more frequently when starting, changing dose, or stopping cinnamon
    • Be particularly cautious with cinnamon supplements rather than culinary use
  2. For patients on midazolam:

    • Consider reducing initial midazolam dose if patient regularly consumes cinnamon supplements
    • Monitor more closely for sedative effects
    • Educate patients about potential for enhanced sedation
  3. For all patients:

    • Maintain consistent cinnamon intake rather than making dramatic changes
    • Report any unusual bleeding, bruising, or excessive sedation promptly

Special Considerations

  • Patients with liver dysfunction may be at higher risk for these interactions due to already reduced drug metabolism
  • Elderly patients may experience more pronounced effects due to age-related changes in drug metabolism
  • Patients taking multiple medications that use the same metabolic pathways (CYP2C9, CYP3A4) are at increased risk for additive effects

The evidence suggests that while moderate culinary use of cinnamon may be acceptable for most patients, those taking warfarin or midazolam should be informed about potential interactions and monitored appropriately, especially when using cinnamon in supplement form or in large quantities.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Cranberry juice ingestion and clinical drug-drug interaction potentials; review of case studies and perspectives.

Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques, 2013

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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