What are the considerations and potential risks for a patient with a history of autoimmune diseases or bleeding disorders, who is on anticoagulant therapy, when using Reishi spores to enhance immune system function or overall health?

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Last updated: January 19, 2026View editorial policy

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Reishi Spores in Patients with Autoimmune Disease and Bleeding Disorders on Anticoagulation

Direct Recommendation

Reishi spores should be avoided in patients with autoimmune diseases requiring immunosuppressive therapy and in those on anticoagulant therapy, particularly if they have bleeding disorders, due to significant risks of immune system dysregulation and potential bleeding complications.


Critical Contraindications in Autoimmune Disease

Patients with active autoimmune diseases requiring systemic immunosuppression should not use Reishi spores. The immunomodulatory effects of Reishi can interfere with immunosuppressive therapy and potentially exacerbate the underlying autoimmune condition 1. This is particularly concerning because:

  • Immune checkpoint modulation risk: Reishi's immune-enhancing properties may trigger or worsen autoimmune flares in patients with conditions like lupus, rheumatoid arthritis, or inflammatory bowel disease 1
  • Treatment interference: The immunostimulatory effects directly counteract the therapeutic goals of immunosuppressive medications used to control autoimmune diseases 1
  • Unpredictable outcomes: Clinical experience with immune-modulating supplements in autoimmune patients is extremely limited and based only on case reports, with variable and unpredictable results 1

Bleeding Risk in Anticoagulated Patients

Reishi spores pose a significant bleeding risk in patients on anticoagulant therapy and should be discontinued. The mechanism involves:

  • Antiplatelet effects: Reishi has documented antiplatelet and anticoagulant properties that can potentiate the effects of therapeutic anticoagulation 2
  • Bleeding disorder amplification: In patients with pre-existing bleeding disorders (hemophilia, thrombocytopenia), the additive anticoagulant effects create unacceptable hemorrhagic risk 1
  • Unpredictable interactions: The combination of Reishi with warfarin, DOACs, or antiplatelet agents has not been studied in controlled trials, making bleeding risk assessment impossible 1

For patients on anticoagulation, even minor bleeding events can escalate. While a blood blister alone would not require stopping anticoagulation 3, the addition of Reishi's anticoagulant properties creates cumulative risk that is clinically unacceptable 1.


Documented Adverse Effects

Reishi is not benign and causes adverse effects in approximately 9% of users. The most common include:

  • Gastrointestinal effects: dry mouth (5%), constipation (4%), diarrhea 4, 5
  • Neurological effects: insomnia (3%), vertigo (3%) 4
  • Dermatological effects: pruritus (3%) 4
  • Potential hepatotoxicity: case reports exist of liver injury 2

Critical toxicity concerns: Laboratory studies demonstrate concentration- and time-dependent cytotoxicity in immune cells, including peripheral blood mononuclear cells from both healthy individuals and patients undergoing chemotherapy 6. This contradicts the assumption that Reishi is universally safe.


Specific Risk Assessment Algorithm

Step 1: Identify Absolute Contraindications

  • Active autoimmune disease requiring immunosuppression → Do not use Reishi 1
  • Current anticoagulation therapy (warfarin, DOACs, heparin) → Do not use Reishi 1, 2
  • Bleeding disorder (hemophilia, von Willebrand disease, severe thrombocytopenia <50,000/mcL) → Do not use Reishi 1
  • Upcoming surgery within 2 weeks → Do not use Reishi 1

Step 2: Assess Relative Contraindications

  • History of autoimmune disease in remission without current immunosuppression → Use extreme caution, close monitoring required 1
  • Antiplatelet therapy alone (aspirin, clopidogrel) → Avoid due to additive bleeding risk 1, 2
  • Mild thrombocytopenia (50,000-100,000/mcL) → Avoid 1

Step 3: Monitor for Complications if Already Using

  • Immediate discontinuation if: new bleeding symptoms, autoimmune flare, gastrointestinal symptoms, or abnormal liver function tests 4, 2
  • Laboratory monitoring: CBC with platelets, PT/INR (if on warfarin), liver function tests 1, 2

Common Clinical Pitfalls

Pitfall 1: Assuming "natural" equals "safe"

  • Reishi has documented cytotoxicity and drug interactions 6, 2
  • The lack of quality control in commercial products means actual content and potency vary widely 2

Pitfall 2: Failing to ask about supplement use

  • Patients often do not volunteer information about herbal supplements 4
  • Specifically ask: "Are you taking any mushroom supplements, including Reishi, lingzhi, or Ganoderma?"

Pitfall 3: Continuing Reishi during immunosuppressive therapy

  • The immunostimulatory effects directly oppose therapeutic immunosuppression 1
  • This applies to all immunosuppressants: corticosteroids, methotrexate, azathioprine, mycophenolate, JAK inhibitors, and biologics 1, 7

Pitfall 4: Not recognizing Reishi spores in stool specimens

  • Reishi spores can be mistaken for parasitic ova in stool examinations 5
  • If parasitic infection is suspected but findings are atypical, ask about Reishi consumption 5

Evidence Quality Assessment

The recommendation against Reishi use in these populations is based on:

  • High-quality guideline evidence regarding autoimmune disease management and anticoagulation 1
  • Mechanistic concerns from pharmacological studies showing anticoagulant and immunomodulatory effects 2
  • Toxicity data from laboratory and clinical studies 4, 6
  • Absence of safety data in the specific high-risk populations (autoimmune disease, bleeding disorders, anticoagulation) 2

The lack of randomized controlled trials in these vulnerable populations, combined with documented risks, mandates a conservative approach prioritizing patient safety over theoretical benefits 1, 2.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Blood Blister Management in Anticoagulated Patients

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Ganoderma lucidum: a cause of pseudoparasitosis.

The Southeast Asian journal of tropical medicine and public health, 2006

Research

Toxicity of a traditional Chinese medicine, Ganoderma lucidum, in children with cancer.

The Canadian journal of clinical pharmacology = Journal canadien de pharmacologie clinique, 2008

Guideline

Management of Jaccoud's Arthropathy

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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