Can Recormon (epoetin‑beta) cause blood clots?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: February 24, 2026View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Can Recormon Cause Blood Clots?

Yes, Recormon (epoetin-beta) significantly increases the risk of blood clots, including deep vein thrombosis, pulmonary embolism, stroke, and myocardial infarction, with a 67% increased relative risk compared to patients not receiving the medication. 1

Magnitude of Thrombotic Risk

The evidence from multiple meta-analyses consistently demonstrates substantial thromboembolic risk:

  • Pooled event rates show 7% thromboembolism risk with epoetin versus 4% in controls 1
  • Relative risk increase of 1.67 (95% CI: 1.35-2.06) for all thromboembolic events including DVT, PE, stroke, MI, and TIA 1
  • The thrombogenic potential exists independent of hemoglobin levels, meaning clot risk persists even when hemoglobin is not excessively elevated 1, 2

Number Needed to Harm

The risk varies dramatically based on baseline thrombotic risk:

  • For patients with 2.5% baseline risk: 1 additional clot per 58 patients treated (95% CI: 36-111) 1
  • For patients with 5% baseline risk: 1 additional clot per 29 patients treated (95% CI: 18-56) 1
  • For patients with 10% baseline risk: 1 additional clot per 15 patients treated (95% CI: 9-28) 1
  • For patients with 20% baseline risk: 1 additional clot per 7 patients treated (95% CI: 5-14) 1

High-Risk Patient Populations Requiring Extreme Caution

Specific patient groups face substantially elevated thrombotic risk:

  • Previous history of thrombosis 1
  • Recent surgery or prolonged immobilization 1
  • Multiple myeloma patients receiving thalidomide or lenalidomide with doxorubicin or corticosteroids 1
  • Patients with chronic kidney disease (92% increased stroke risk, absolute risk 5.0% vs 2.6%) 1, 2
  • Patients with underlying coronary artery disease or symptomatic angina 1

Critical Management Principles

When Recormon must be used despite thrombotic risk:

  • Control blood pressure before initiating therapy and monitor regularly throughout treatment 1, 2
  • Target hemoglobin levels of 10-12 g/dL maximum; never exceed 12 g/dL 1, 2
  • Discontinue immediately if hemoglobin rises above 12 g/dL or increases by more than 1 g/dL in any 2-week period 3
  • Monitor weekly for signs of thromboembolism: leg pain/swelling, chest pain, shortness of breath, neurological changes 3
  • Increase heparinization in hemodialysis patients to prevent clotting in dialysis equipment 4

Important Caveat About Anticoagulation

There are no data from randomized trials investigating whether concomitant use of anticoagulants or aspirin reduces the thrombotic risk associated with Recormon 1, 3. The American Society of Clinical Oncology explicitly states this evidence gap, meaning clinicians cannot assume anticoagulation provides protection against epoetin-induced thrombosis 1.

Common Pitfall to Avoid

Do not assume that maintaining "normal" hemoglobin levels eliminates clot risk—the thrombogenic mechanism operates independently of hemoglobin concentration 1, 2. Even patients with hemoglobin below 12 g/dL remain at increased thrombotic risk while receiving Recormon 1.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Erythropoietin and Stroke Risk

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Safety of Epoetin with Apixaban and Aspirin

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.