What is the recommended dosage of enoxaparin (Low Molecular Weight Heparin) for Deep Vein Thrombosis (DVT) prophylaxis?

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Last updated: October 17, 2025View editorial policy

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Enoxaparin Dosage for DVT Prophylaxis

The standard recommended dosage of enoxaparin for DVT prophylaxis is 40 mg subcutaneously once daily for most adult patients. 1

Standard Dosing Recommendations

  • Enoxaparin 40 mg subcutaneously once daily is the standard prophylactic dose for medical and surgical patients 2, 1
  • Treatment should continue for the duration of hospitalization or until the patient is fully ambulatory 1
  • For surgical patients, prophylaxis should continue for at least 7-10 days post-procedure 1

Special Population Dosing Adjustments

Renal Impairment

  • For patients with severe renal insufficiency (creatinine clearance <30 mL/min), reduce the dose to 30 mg subcutaneously once daily 3, 1, 4
  • Renal clearance of enoxaparin is reduced by 31% in moderate renal impairment (30-60 mL/min) and 44% in severe renal impairment (<30 mL/min) 3, 4

Obesity

  • For patients with obesity (BMI >30 kg/m²), consider intermediate doses of 40 mg subcutaneously every 12 hours or weight-based dosing of 0.5 mg/kg subcutaneously every 12 hours 2, 1, 5
  • Standard fixed dosing may be inadequate in morbidly obese patients 5, 6
  • A study of morbidly obese patients showed that weight-based dosing at 0.5 mg/kg once daily resulted in appropriate anti-Xa levels without excessive anticoagulation 5

Pregnancy

  • For pregnant women with class III obesity requiring thromboprophylaxis, intermediate doses of enoxaparin (0.5 mg/kg subcutaneously every 12 hours) are suggested 3

Administration Timing Considerations

  • For surgical patients, initiate enoxaparin 2-4 hours preoperatively or 10-12 hours preoperatively when neuraxial anesthesia is planned 2, 1
  • Avoid administration within 10-12 hours before neuraxial anesthesia to reduce the risk of spinal hematoma 1
  • For prophylactic doses after neuraxial anesthesia, enoxaparin may be started as early as 4 hours after catheter removal but not earlier than 12 hours after the block was performed 3

Monitoring Recommendations

  • Routine anti-Xa monitoring is not required for most patients receiving prophylactic doses 4
  • For patients with severe renal impairment on prolonged therapy, consider monitoring anti-Xa levels with a target range of 0.5-1.5 IU/mL 3
  • Anti-Xa levels should be measured 4-6 hours after dosing, after the patient has received 3-4 doses 3

Common Pitfalls and Caveats

  • Failure to adjust dosing in renal impairment can lead to drug accumulation and increased bleeding risk 1, 4
  • Standard fixed dosing may be inadequate in obese patients, potentially leading to treatment failure 5, 6
  • Concomitant use with other antiplatelet or anticoagulant medications increases bleeding risk 1
  • Timing of administration relative to neuraxial procedures is critical to prevent spinal hematoma 3, 1

References

Guideline

Enoxaparin Dosing and Administration for DVT Prophylaxis and Stroke Prevention

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Dosis de Enoxaparina para Prevención y Tratamiento de Trombosis Venosa Profunda

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

DVT Prophylaxis for Elderly Patients with CKD Stage 3

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Comparison of standard versus adjusted dose of enoxaparin for venous thromboembolism prophylaxis in patients with obesity and cancer.

Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners, 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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