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Drug Interactions between pemivibart and sars-cov-2 (covid-19) mrna-1273 (bivalent booster) vaccine

This report displays the potential drug interactions for the following 2 drugs:

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Interactions between your drugs

Moderate

SARS-CoV-2 (COVID-19) mRNA-1273 bivalent vaccine pemivibart

Applies to: sars-cov-2 (covid-19) mrna-1273 (bivalent booster) vaccine and pemivibart

ADJUST DOSING INTERVAL: The administration of pemivibart within two weeks after receiving a SARS-CoV-2 (COVID-19) vaccine may be associated with a diminished or suboptimal immunologic response to the vaccine. The mechanism of this interaction has not been fully described in product labeling. Pemivibart exerts its effects by binding to the virus' spike protein receptor binding domain (RBD) thereby inhibiting virus attachment to the human ACE2 receptor on host cells. Therefore, it may also bind to the viral spike protein introduced by a COVID-19 vaccine, potentially interfering with the vaccine's ability to mount an adequate immune response. The timing of COVID-19 vaccination following the receipt of pemivibart is not discussed in product labeling. However, the U.S. Centers for Disease Control and Prevention (CDC) advises that people who are moderately or severely immunocompromised should receive the COVID-19 vaccination according to the recommended schedule. Clinical data surrounding a loss of efficacy of the COVID-19 vaccine if given prior to, or after pemivibart administration are not available.

MANAGEMENT: Pemivibart should be administered at least 2 weeks after the receipt of a COVID-19 vaccination to avoid the potential loss of vaccine efficacy. Additionally, current immunization guidelines for people who are moderately or severely immunocompromised recommend that COVID-19 vaccination be given in accordance with the recommended vaccine schedule, and pemivibart not be given as a substitution for COVID-19 vaccination.

References

  1. (2024) "Product Information. Pemgarda (pemivibart)." Invivyd, Inc.
  2. CDC. Centers for Disease Control and Prevention (2024) Interim clinical considerations for use of COVID-19 vaccines in the United States https://www.cdc.gov/vaccines/covid-19/clinical-considerations/interim-considerations-us.html#COVID-19-vaccination-pemivibart
  3. FDA. U.S Food & Drug Administration (2024) Frequently asked auestions on the emergency use authorization for Pemgarda (pemivibart) https://www.fda.gov/media/177066/download?attachment

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Drug and food interactions

No alcohol/food interactions were found. However, this does not necessarily mean no interactions exist. Always consult your healthcare provider.

Therapeutic duplication warnings

No warnings were found for your selected drugs.

Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.


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Drug Interaction Classification

These classifications are only a guideline. The relevance of a particular drug interaction to a specific individual is difficult to determine. Always consult your healthcare provider before starting or stopping any medication.
Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan.
Unknown No interaction information available.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.