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There is no human clinical trial establishing any effective or safe human dose, oral or injected

[3] Ondansetron demonstrates selective antagonism at the 5-HT3 receptor sites, which are believed to play a crucial role in the pathophysiology of nausea and vomiting responses

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7b) In contrast to the previous study that showed reduced proliferation with high ROS secondary to G6PD inhibition, proliferation in this study was increased when ROS were increased in the setting of normal G6PD activity