Drug Interactions between adagrasib and Brukinsa
This report displays the potential drug interactions for the following 2 drugs:
- adagrasib
- Brukinsa (zanubrutinib)
Interactions between your drugs
zanubrutinib adagrasib
Applies to: Brukinsa (zanubrutinib) and adagrasib
Consumer information for this interaction is not currently available.
ADJUST DOSE: Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of zanubrutinib, which is primarily metabolized by the isoenzyme. When zanubrutinib was coadministered with the potent CYP450 3A4 inhibitor itraconazole (200 mg once daily), zanubrutinib peak plasma concentration (Cmax) and systemic exposure (AUC) increased 157% and 278%, respectively, in healthy volunteers. When zanubrutinib was coadministered with another CYP450 3A4 inhibitor, clarithromycin (250 mg twice daily), zanubrutinib Cmax and AUC increased 101% and 92%, respectively, in patients with B-cell lymphoma. Increased zanubrutinib exposure may potentiate the risk of toxicities such as Haemorrhage, infection, cytopenias, malignancies, and serious cardiac arrhythmias, primarily atrial fibrillation and atrial flutter.
MANAGEMENT: The dosage of zanubrutinib should be reduced to 80 mg once daily when used concomitantly with potent CYP450 3A4 inhibitors. The manufacturer recommends reducing the dosage of zanubrutinib to 80 mg twice daily, when used concomitantly with clarithromycin 250 mg twice daily, and to 80 mg once daily when used concomitantly with clarithromycin 500 mg twice daily. Close clinical monitoring for development of zanubrutinib-related toxicities, further dosage adjustment, and/or withholding treatment in accordance with product labeling is advised. Following discontinuation, of the potent CYP450 3A4 inhibitor, the previous dosage of zanubrutinib may be resumed. Additional consultation with individual package labeling, as well as relevant institutional protocols, may be advisable for further guidance.
Drug and food interactions
zanubrutinib food
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.
adagrasib food
Applies to: adagrasib
You should avoid consumption of grapefruit and grapefruit juice during approximately the first 8 days of treatment with adagrasib. During this time, grapefruit juice may increase the blood levels of adagrasib. This may increase the risk of side effects such as diarrhea, fatigue, musculoskeletal pain, hepatotoxicity, renal impairment, and an irregular heart rhythm that may be serious and potentially life-threatening. You should seek immediate medical attention if you develop sudden dizziness, lightheadedness, fainting, shortness of breath, or heart palpitations during treatment with adagrasib. Talk to your doctor if you have any questions or concerns. 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.
See also
Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
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. | |
No interaction information available. |
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
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