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Take note that these dose ranges are an approximation, rely on individual conduct/task, and in certain species depending on only 1 or 2 studies and drug administrations. The species dissimilarities might be as a result of pharmacokinetics and metabolism discrepancies, as well as the physiology of the specific animal models. It is usually probably that immediate mg/kg comparison is not really appropriate across species and interspecies scaling variable is essential for the significant comparison.

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The most common route of administration for rodents was subcutaneous or intraperitoneal. For just a summary with the doses, routes of administration and behavioural results by species, see Tables 2 and ​and33.

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