Drug Interactions between rozanolixizumab and tislelizumab
This report displays the potential drug interactions for the following 2 drugs:
- rozanolixizumab
- tislelizumab
Interactions between your drugs
rozanolixizumab tislelizumab
Applies to: rozanolixizumab and tislelizumab
Consumer information for this interaction is not currently available.
MONITOR: Concomitant use of a human neonatal Fc receptor (FcRn) blocker like efgartigimod alfa or rozanolixizumab may decrease the plasma concentrations and therapeutic effects of medications that bind to the FcRn such as immune globulins, monoclonal antibodies, or antibody derivatives containing the human Fc domain of the IgG subclass (e.g., abatacept, aflibercept, asfotase alfa, belatacept, dulaglutide, etanercept, luspatercept, rilonacept, romiplostim, and some recombinant coagulation factors). FcRn blockers target the FcRn, a widely expressed receptor that plays a critical role in recycling and maintaining homeostatic levels of circulating IgG and other antibodies by preventing their cellular degradation. For example, reduced serum concentrations of these products are anticipated to occur if they are administered concomitantly or within 2 weeks after the administration of rozanolixizumab.
MANAGEMENT: Due to the potential for their reduced effectiveness, close monitoring is recommended if medications that bind to the human neonatal Fc receptor are required during concomitant treatment with FcRn blockers. When long-term use of such medications is required, consider discontinuing the FcRn blocker and using alternative therapies. Some authorities recommend that initiation of treatment with these products should be delayed to 2 weeks after the last dose of any given treatment cycle of either FcRn blocker. Individual product labeling should be consulted for further guidance.
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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