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In patients treated with potent inducers of CYP3A4 (i.e., phenytoin, carbamazepine, and rifampin), the clearance of ondansetron was significantly increased and ondansetron blood concentrations were decreased
Retrieved 30 December 2016
[4] Where published studies do not report a toxicological signal, the correct interpretation is not reported under the tested experimental conditions, not fully excluded. This distinction is important because many published studies involving 5-Amino-1MQ were designed primarily to evaluate NNMT-related biological mechanisms or model-specific metabolic endpoints, rather than to serve as dedicated toxicology programs
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