What is the maximum recommended dose of vitamin K (phytonadione) for an adult?

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Maximum Recommended Dose of Vitamin K for Adults

The maximum recommended single dose of vitamin K (phytonadione) for adults is 10 mg, with higher doses (up to 25-50 mg) reserved only for rare, severe cases of anticoagulant-induced bleeding, though doses exceeding 10 mg can create a prothrombotic state and should be avoided in most clinical situations. 1, 2, 3

Standard Maximum Dosing by Clinical Scenario

Emergency Anticoagulation Reversal

  • Maximum single dose: 10 mg IV administered by slow infusion over 30 minutes to minimize anaphylactoid reaction risk (approximately 3 per 100,000 doses) 1, 2, 3
  • For life-threatening warfarin-associated bleeding, combine 10 mg IV vitamin K with four-factor prothrombin complex concentrate for rapid INR correction 2, 3
  • Do not exceed 10 mg per dose as higher amounts induce a prothrombotic state and prevent re-anticoagulation for days 1

Anticoagulant-Induced Prothrombin Deficiency

  • Initial dose: 2.5 to 10 mg, or up to 25 mg in rare instances 3
  • In exceptional circumstances, 50 mg may be required, though this represents the absolute upper limit 3
  • The FDA label specifies these higher doses (25-50 mg) are for rare, severe cases only 3

Rate of Administration

  • Never exceed 1 mg per minute when administering intravenously 3
  • Slow infusion over 30 minutes is recommended to minimize anaphylactoid reactions 1, 2

Context-Specific Maximum Doses

Parenteral Nutrition

  • Weekly IV supply of 250-500 mcg (0.25-0.5 mg) phylloquinone from lipid emulsions is sufficient for maintenance 4, 2
  • Adult multivitamin preparations provide additional 150 mcg (0.15 mg) to maintain carboxylation status 4, 2
  • Caution: Doses >150 mcg may cause vitamin K antagonist resistance in patients on warfarin 4, 2

Bariatric Surgery Patients

  • For vitamin K deficiency: 10 mg IM or subcutaneous, followed by 1-2 mg/week parenterally or orally 4
  • After biliopancreatic diversion: 300 mcg (0.3 mg) daily as part of routine supplementation 4

Cystic Fibrosis Patients

  • Adults: 1-10 mg/day depending on age and risk factors 4
  • Higher doses may be considered for those with documented low vitamin K levels or on long-term antibiotics 4
  • No known adverse effects from phylloquinone supplementation, making toxicity not a concern 4

Liver Disease

  • 10 mg IV or oral as a diagnostic/therapeutic trial, with INR reassessment after 12-24 hours 1
  • A decrease in INR ≥0.5 within 24-72 hours confirms vitamin K deficiency component 1
  • Vitamin K has minimal efficacy in decompensated chronic liver disease when hepatic synthetic function is severely impaired 1

Critical Safety Considerations

Why 10 mg Is the Practical Maximum

  • Doses exceeding 10 mg create a prothrombotic state and prevent effective re-anticoagulation for several days 1
  • The risk-benefit ratio favors lower doses, as vitamin K takes >12 hours to begin correcting hemostatic defects 1
  • In a study of mainly cirrhotic patients receiving 10 mg IV daily for 3 days, the overall adjusted INR decrease was only 0.3, suggesting minimal clinical impact of repeated high doses 5

Route-Specific Concerns

  • Subcutaneous administration is ineffective in correcting coagulopathy in liver disease 1
  • IV administration carries anaphylactoid risk (3 per 100,000 doses) with potential for cardiac arrest, severe hypotension, arrhythmias, dyspnea, or bronchospasm 1
  • Oral administration shows similar INR reduction by 24 hours compared to IV, though IV has more rapid onset 2, 6

Common Pitfalls to Avoid

Overcorrection Risk

  • High-dose IV vitamin K (>5 mg) causes overcorrection (INR <2.0) more frequently than lower doses 7
  • For INR 6-10, use 0.5 mg IV or 2.5 mg oral; for INR >10, use 1 mg IV or 5 mg oral 3, 7
  • Oral doses of 1-2.5 mg reduce INR from 5.0-9.0 to 2.0-5.0 within 24-48 hours without overcorrection 8

Inappropriate Use in Liver Disease

  • Routine correction of elevated INR with vitamin K is not supported by evidence in chronic liver disease without active bleeding 1
  • Vitamin K is only effective when true deficiency exists (prolonged antibiotics, malnutrition, cholestasis), not in hepatic synthetic dysfunction 1
  • Factors associated with poor response include higher body weight, presence of cirrhosis, and higher bilirubin levels 5

Monitoring Requirements

  • Re-check INR 12-24 hours after administration 1, 3
  • If INR remains abnormal, monitor every 6-8 hours for the next 24-48 hours 1
  • If prothrombin time has not shortened satisfactorily in 6-8 hours after parenteral administration, repeat the dose 3

Algorithm for Dose Selection

For warfarin over-anticoagulation without bleeding:

  • INR 5-9: 1-2.5 mg oral 8, 9
  • INR >10: 5 mg oral 8, 9

For warfarin-associated bleeding:

  • Minor bleeding: 2.5-5 mg IV 3
  • Major bleeding: 10 mg IV (maximum) + prothrombin complex concentrate 1, 2, 3

For suspected vitamin K deficiency in liver disease:

  • Diagnostic/therapeutic trial: 10 mg IV or oral, reassess INR in 12-24 hours 1

For maintenance in special populations:

  • Parenteral nutrition: 150-500 mcg weekly 4, 2
  • Cystic fibrosis: 1-10 mg daily 4
  • Post-bariatric surgery: 0.3 mg daily (BPD) or as needed 4

References

Guideline

Administration of Vitamin K for Abnormal Liver Function

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Vitamin K Administration Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

The use of vitamin K in patients on anticoagulant therapy: a practical guide.

American journal of cardiovascular drugs : drugs, devices, and other interventions, 2004

Research

Management and dosing of warfarin therapy.

The American journal of medicine, 2000

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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