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U.S. Department of Health and Human Services


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Emend (aprepitant) capsules

Detailed View: Safety Labeling Changes Approved By FDA Center for Drug Evaluation and Research (CDER) – March 2010


Summary View



Clinical Trials Experience
  • section (including Table 2) was updated to include the adverse experience data from the sponsor's completed postmarketing study.


Post-Marketing Trial
  • Entire Section Updated
  • In a postmarketing, multicenter, randomized, double-blind, parallel-group, clinical study in 848 cancer patients, the aprepitant regimen (N=430) was compared with a standard of care therapy (N=418) in patients receiving a moderately emetogenic chemotherapy regimen that included...