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Published on: July 15, 2019
Interaction between warfarin and molnupiravir in a patient with coronavirus disease 2019 infection
Hikari Mizutani1, Tetsuro Koide1, Takashi Omura2
1Department of Pharmacy, Kuwana City Medical Center, Kuwana, Mie Prefecture, Japan.
Abstract:
Molnupiravir is a novel antiviral agent for coronavirus disease 2019 (COVID-19) treatment. Warfarin is an oral anticoagulation agent with difficult management due to drug interactions. Here, we describe a case of international normalized ratio (INR) prolongation in a patient who administrated warfarin with molnupiravir for COVID-19. An increased INR at 3.80, enough to discontinue warfarin, was observed on the fifth day of molnupiravir therapy, although the warfarin dose and INR were stable at 4 mg/day and approximately 2.0 before the molnupiravir initiation, respectively. Factors that affect the INR, such as severe COVID-19, cytokine, diet, liver dysfunction, and the concomitant use of medications other than molnupiravir, were unlikely in this patient. This case suggests that healthcare physicians should be aware of the possibility of drug interaction between molnupiravir and warfarin.
Insights
Molnupiravir may increase the blood-thinning effect of warfarin, leading to a higher risk of bleeding. This drug interaction necessitates careful monitoring of international normalized ratio (INR) in patients taking both medications.
Area of Science:
- Pharmacology
- Infectious Diseases
- Internal Medicine
Background:
- Molnupiravir is an antiviral medication used for treating coronavirus disease 2019 (COVID-19).
- Warfarin is an oral anticoagulant requiring careful management due to potential drug interactions.
- Drug interactions with molnupiravir are not fully characterized, posing a risk in patients with comorbidities.
Observation:
- A case study documented a patient receiving both warfarin and molnupiravir for COVID-19 treatment.
- The patient experienced a significant increase in international normalized ratio (INR) to 3.80 after five days of molnupiravir therapy.
- This INR elevation occurred despite stable warfarin dosage and baseline INR prior to molnupiravir initiation.
Findings:
- The observed INR prolongation was attributed to a potential drug interaction between molnupiravir and warfarin.
- Other common factors influencing INR, including disease severity, cytokine storm, diet, liver function, and other medications, were ruled out.
- This suggests a direct interaction effect of molnupiravir on warfarin's anticoagulant activity.
Implications:
- Healthcare providers should exercise caution when prescribing molnupiravir to patients on warfarin therapy.
- Close monitoring of INR levels is crucial to detect and manage potential over-anticoagulation.
- Further research is warranted to elucidate the mechanism of this drug interaction and establish clinical guidelines.
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