Drug Interactions between fludarabine and In-111 Zevalin
This report displays the potential drug interactions for the following 2 drugs:
- fludarabine
- In-111 Zevalin (ibritumomab)
Interactions between your drugs
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)
- 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.
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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