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Drug Interactions between fludarabine and In-111 Zevalin

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

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Interactions between your drugs

Moderate

fludarabine ibritumomab tiuxetan

Applies to: fludarabine and In-111 Zevalin (ibritumomab)

MONITOR: Administration of radiolabeled ibritumomab tiuxetan (after pretreatment with rituximab) results in severe and prolonged cytopenia that is generally reversible, and the risk may be increased after prior therapy with fludarabine-containing regimens. In a clinical trial in which yttrium-90 radiolabeled ibritumomab tiuxetan was administered as consolidation after prior first-line chemotherapy, a higher frequency of severe and prolonged neutropenia and thrombocytopenia was observed in patients who had received yttrium-90 radiolabeled ibritumomab tiuxetan within 4 months after a combination chemotherapy of fludarabine with mitoxantrone and/or cyclophosphamide compared to those who had received any other chemotherapy.

MANAGEMENT: Clinicians should be aware that there may be an increased risk of hematologic toxicity when radiolabeled ibritumomab tiuxetan is administered shortly (within 4 months) after fludarabine-containing regimens. Complete blood cell and platelet counts should be monitored closely in accordance with product labeling recommendations.

References (1)
  1. Cerner Multum, Inc. "UK Summary of Product Characteristics."

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.