Infusion reactions were also numerically higher in the EMEND® group, but the difference did not reach statistical significance (OR = 4.35; 95%CI: 0.83 to 22.8).
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A real-world study to evaluate the safety and efficacy of three injectable neurokinin-1 receptor antagonist formulations for the prevention of chemotherapy-induced nausea and vomiting in cancer patients.
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The sentences
Over all cycles of chemotherapy, patients who received IV EMEND® had an increased risk of infusion site reactions compared to patients in the CINVANTI® group (OR = 4.35; 95%CI: 0.83 to 6.84), but the incremental risk failed to reach statistical significance, likely due to the small number of events (Table 6 ).