What is the proper technique for administering a 10 mg intramuscular injection of vitamin K1 (phytonadione)?

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Last updated: February 8, 2026View editorial policy

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Administration of Vitamin K 10mg Injection

For a 10 mg dose of vitamin K (phytonadione), administer intravenously by slow infusion over 30 minutes, never exceeding 1 mg per minute, as rapid IV administration carries a risk of anaphylactic reactions that can result in cardiac arrest. 1, 2

Route Selection and Critical Safety Considerations

Intravenous Administration (Preferred for Urgent Situations)

  • Dilute the 10 mg dose in 0.9% Sodium Chloride, 5% Dextrose, or 5% Dextrose and Sodium Chloride Injection using preservative-free diluents, and administer immediately after mixing 2
  • Infuse slowly over 30 minutes, not exceeding 1 mg per minute to minimize the risk of severe anaphylactoid reactions 1, 2
  • Anaphylactic reactions occur in 3 per 100,000 IV doses via a non-IgE mechanism, likely due to the polyoxyethylated castor oil solubilizer, and can cause cardiac arrest, severe hypotension, bradycardia/tachycardia, dyspnea, and bronchospasm 1, 3, 4
  • Protect the solution from light at all times during preparation and administration 2
  • Discard unused portions of diluted solution and unused vial contents immediately after use 2

Intramuscular Administration (Alternative Route)

  • The FDA label states IM administration should be considered only when IV or subcutaneous routes are unavoidable, as IM injection carries risks of local tissue reactions 2
  • Administer deep intramuscular injection if this route is selected, though IV is generally preferred for the 10 mg dose 2
  • Scleroderma-like skin reactions can develop at IM injection sites, appearing as ivory indurated morphoeiform plaques ("cowboy's belt with revolver" pattern) that may persist for years after injection 5
  • Severe anaphylactoid reactions have been reported with IM administration, including cases requiring emergency cesarean section 6

Oral Administration (Off-Label Alternative)

  • Injectable vitamin K can be administered orally as an effective and safe alternative when the IV route poses excessive risk (e.g., history of anaphylaxis) or for non-emergency situations 3, 7, 8
  • Oral administration achieves 95% INR reduction within 24 hours and carries no risk of anaphylaxis, making it the preferred route for non-bleeding elevated INR scenarios 9, 8
  • The injectable formulation can be given undiluted orally or mixed with juice/water for palatability 7

Clinical Context for 10 mg Dosing

Life-Threatening Bleeding

  • 10 mg IV vitamin K should always be co-administered with 4-factor prothrombin complex concentrate (PCC) 25-50 U/kg for immediate reversal in life-threatening bleeding 1, 3, 4
  • Vitamin K alone is insufficient for emergent reversal, as PCC achieves INR <1.5 within 5-15 minutes while vitamin K alone takes hours 3, 9
  • Co-administration is essential because factor VII in PCC has only a 6-hour half-life, requiring vitamin K to stimulate endogenous production of vitamin K-dependent factors 1, 3, 4

Major Non-Life-Threatening Bleeding

  • 5-10 mg IV vitamin K by slow infusion over 30 minutes is appropriate for major bleeding without hemodynamic instability 1, 3, 9
  • Consider adding PCC if bleeding is at critical sites (intracranial, intraspinal, intraocular, pericardial, retroperitoneal) or causing significant hemodynamic compromise 4

Severe Over-Anticoagulation Without Bleeding

  • For INR >10 without bleeding, 5-10 mg can be given, but oral administration is preferred over IV to avoid anaphylaxis risk 1, 3, 9

Critical Dosing Caveats

  • Never exceed 10 mg vitamin K in most clinical situations, as higher doses (>10 mg) create a prothrombotic state and cause warfarin resistance lasting up to one week 1, 3, 9
  • High-dose vitamin K may require heparin bridging when warfarin needs to be resumed after the vitamin K effect wears off 3, 9
  • In mechanical valve patients, use lower doses (1-2 mg oral) to avoid difficulty achieving therapeutic INR post-procedure and increased thrombosis risk 4

Monitoring After Administration

  • Recheck INR 15-60 minutes after PCC administration (if given concurrently) to assess degree of correction 4
  • Monitor INR regularly over the next week, as a minority of patients take over a week to clear warfarin and require additional vitamin K 1, 4
  • Consider thromboprophylaxis as early as possible after bleeding control, as PCC use increases risk of venous and arterial thrombosis during recovery 1, 4

Common Pitfalls to Avoid

  • Do not administer as rapid IV push, as this dramatically increases anaphylaxis risk 1, 2
  • Do not use subcutaneous route for the 10 mg dose, as absorption is unpredictable and the FDA label recommends IV or IM for this dose 2
  • Do not give vitamin K alone for life-threatening bleeding, as it takes hours to work and must be combined with PCC for immediate effect 3, 9
  • Do not use preservative-containing diluents, especially in newborns, as benzyl alcohol has been associated with toxicity 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Vitamin K Injection Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Warfarin Reversal in Significant Bleeding or Emergency Surgery

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

"Cowboy's belt with revolver" scleroderma caused by vitamin K1 injections.

Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia, 2012

Guideline

Vitamin K Administration for INR Reduction

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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