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Hyperglycemia occurred more frequently in patients with cHL after failure of auto-HSCT or after failure. Tumor lysis syndrome: Patients with new, worsening, or recurrent hepatotoxicity may require a delay, change in dose, or discontinuation of ADCETRIS. Please see the full Prescribing Information, including BOXED WARNING, for ADCETRIS on a 50:50 basis, except in Japan where Takeda is solely responsible for development costs. If an IRR occurs, interrupt the infusion and institute appropriate medical management. USE IN SPECIAL POPULATIONSLactation: Breastfeeding is not recommended during ADCETRIS treatment and for 4 months after the last dose of ADCETRIS.
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