What are the potential interactions between Apixaban (Direct Oral Anticoagulant) 5mg twice a day and Uridine-5' Monophosphate, Disodium?

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Last updated: July 14, 2025View editorial policy

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Apixaban and Uridine-5' Monophosphate, Disodium Interaction

There is no documented clinically significant interaction between apixaban 5mg twice daily and uridine-5' monophosphate, disodium that would require dose adjustment or contraindicate their concurrent use.

Understanding Apixaban's Metabolism and Interaction Pathways

Apixaban is a direct factor Xa inhibitor with the following key pharmacokinetic characteristics:

  • Metabolized primarily via CYP3A4 enzyme pathway
  • Substrate for P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP) transporters
  • Has approximately 50% oral bioavailability
  • Half-life of approximately 12 hours
  • Approximately 27% renal excretion 1

Known Interaction Mechanisms for Apixaban

Drug interactions with apixaban typically occur through:

  1. CYP3A4 inhibition or induction
  2. P-gp inhibition or induction
  3. BCRP inhibition or induction

When these pathways are affected, apixaban plasma concentrations can increase (with inhibitors) or decrease (with inducers), potentially leading to increased bleeding risk or reduced efficacy, respectively 2.

Analysis of Uridine-5' Monophosphate, Disodium

Uridine-5' monophosphate, disodium is not documented in the available guidelines as:

  • A CYP3A4 inhibitor or inducer
  • A P-gp inhibitor or inducer
  • A BCRP inhibitor or inducer

None of the comprehensive drug interaction guidelines for apixaban mention uridine-5' monophosphate, disodium as a medication of concern 2.

Clinical Decision Making

When to Monitor for Potential Interactions

While there is no specific documented interaction, it is worth noting that:

  • Guidelines recommend monitoring DOAC plasma concentrations when a relevant drug-drug interaction is expected and switching to another anticoagulant is not an option 2
  • For apixaban, the most concerning interactions occur with strong dual inhibitors of both CYP3A4 and P-gp 2

Precautions with Other Medications

Be vigilant about other medications that might be co-administered:

  • Strong CYP3A4 and P-gp inhibitors (e.g., ketoconazole, ritonavir) require 50% dose reduction of apixaban if on 5-10mg twice daily regimen 2
  • Strong CYP3A4 and P-gp inducers (e.g., rifampin, carbamazepine) should be avoided due to risk of reduced efficacy 2
  • Common over-the-counter medications like NSAIDs and aspirin can increase bleeding risk when combined with apixaban 3

Monitoring Recommendations

While routine monitoring is not required for apixaban and there is no known interaction with uridine-5' monophosphate, disodium, clinicians should:

  1. Monitor for any unexpected signs of bleeding or thrombosis
  2. Consider anti-Xa assay measurement if there is concern about extreme apixaban levels
  3. Be particularly vigilant in patients with renal impairment, as apixaban clearance may be affected

Common Pitfalls to Avoid

  1. Assuming all nucleotide-based compounds have similar interaction profiles
  2. Overlooking potential interactions with other concurrently administered medications
  3. Failing to consider patient-specific factors that might affect apixaban levels (age, weight, renal function)
  4. Not educating patients about potential interactions with over-the-counter medications and supplements

In conclusion, while there is no documented interaction between apixaban and uridine-5' monophosphate, disodium, clinicians should remain vigilant for any unexpected changes in anticoagulation effect and continue to monitor for bleeding or thrombotic complications.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 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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