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Drug Interactions between Brukinsa and COVID-19 mRNA (Pfizer) vaccine

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

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Interactions between your drugs

Moderate

zanubrutinib SARS-CoV-2 (COVID-19) mRNA-LNP vaccine (cvx 309)

Applies to: Brukinsa (zanubrutinib) and COVID-19 mRNA (Pfizer) vaccine

Consumer information for this interaction is not currently available.

MONITOR: The administration of SARS-CoV-2 (COVID-19) vaccines to immunosuppressed patients is generally safe, but may be associated with a diminished or suboptimal immunologic response due to antibody inhibition. Observational studies in adults who completed a 1 or 2 dose COVID-19 vaccine series revealed lower efficacy against SARS-CoV-2 infection and COVID-19 disease in immunocompromised adults when compared with the general population. Such patients may include those who have recently received or are receiving immunosuppressive agents, antilymphocyte globulins, alkylating agents, antimetabolites, radiation, some antirheumatic agents, high dosages of corticosteroids or adrenocorticotropic agents (e.g., greater than or equal to 2 mg/kg/day or 20 mg/day of prednisone or equivalent for 14 consecutive days or more), or long-term topical or inhaled corticosteroids.

MANAGEMENT: In general, the U.S. Advisory Committee on Immunization Practices (ACIP) recommends administering SARS-CoV-2 (COVID-19) vaccines to moderately or severely immunosuppressed patients. However, depending on the patient's age, concurrent medical condition(s), medication(s), and prior receipt of a COVID-19 vaccine, additional doses, boosters, or revaccination may be appropriate to improve the patient's immune response and the vaccine's efficacy. Whenever possible, COVID-19 vaccine administration should be completed at least 2 weeks before initiation or resumption of immunosuppressive therapies. Revaccination is often recommended in patients who received 1 or more doses of a COVID-19 vaccine prior to or during hematopoietic cell transplantation (HCT) or chimeric antigen receptor (CAR) T-cell therapy and may be considered in patients who were treated with B-cell-depleting therapy over a limited period (e.g., as part of a treatment regimen for certain malignancies). The ACIP recommends that patients who receive B-cell-depleting therapies on a continuing basis receive their COVID-19 vaccine(s) approximately 4 weeks before the next scheduled therapy. COVID-19 vaccines may generally be administered to patients receiving corticosteroids as replacement therapy (e.g., for Addison's disease). Decisions to alter the schedule or frequency of immunosuppressive therapy in order to complete COVID-19 vaccination should consider the individual's risks relative to their underlying condition. Prescribing information and relevant guidelines should be consulted for the most up to date information.

Drug and food/lifestyle interactions

Major

zanubrutinib food/lifestyle

Applies to: Brukinsa (zanubrutinib)

Grapefruit juice and Seville orange juice can increase the blood levels of zanubrutinib. This may increase side effects such as rash, diarrhea, constipation, cough, hemorrhage, development of other cancers, abnormal heart rhythm, and impaired bone marrow function resulting in low numbers of different types of blood cells. You may also be more likely to develop anemia, bleeding problems, or infections due to low blood cell counts. You should avoid the consumption of Seville oranges, Seville orange juice, grapefruit and grapefruit juice during treatment with zanubrutinib. Be sure to take the medication at approximately the same time(s) everyday to maintain consistent blood levels and effects. Talk to your doctor or pharmacist if you have questions on how to take this or other medications you are prescribed. It is important to tell your doctor about all other medications you use, including vitamins and herbs. Do not stop using any medications without first talking to your doctor.

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.