“In this paragraph “medicinal product” has the same meaning as in theHuman Medicines Regulations 2012 (S.I. 2012/1916) (see regulation 2 of those Regulations).”
“2.(1) In these Regulations “medicinal product” means— (a) any substance or combination of substances presented as having properties of preventing or treating disease in human beings; or (b) any substance or combination of substances that may be used by or administered to human beings with a view to— (i) restoring, correcting or modifying a physiological function by exerting a pharmacological, immunological or metabolic action, or (ii) making a medical diagnosis. (2) These Regulations do not apply to— (a) whole human blood; or (b) any human blood component, other than plasma prepared by a method involving an industrial process.” (a) any substance or combination of substances presented as having properties of preventing or treating disease in human beings; or (b) any substance or combination of substances that may be used by or administered to human beings with a view to— (i) restoring, correcting or modifying a physiological function by exerting a pharmacological, immunological or metabolic action, or (ii) making a medical diagnosis. (a) whole human blood; or (b) any human blood component, other than plasma prepared by a method involving an industrial process.”
“residual sedation, confusion, disorientation and headaches. Nausea and vomiting have also been reported. Larger doses may result in loss of consciousness and cause asphyxiation by oxygen displacement.”
“Prosecutions relating to the sale of nitrous oxide as a psychoactive substance under the 2016 Act are flawed on at least three grounds a) Nitrous oxide is a medicine – and has been for over a century and a half. b) Nitrous oxide is not proved to be psychoactive under the meaning of the Act. c) The effects of nitrous oxide on the brain are not mediated by a direct effect on the central nervous system.”
“It would be possible to prove that nitrous oxide is psychoactive through a direct effect on the brain by conducting a state-of-the-art brain imaging study in humans. This would involve human volunteers being given nitrous oxide in a scanner and the impact of the gas on the binding of a radio-tracer that labels either the glutamate, endorphin or dopamine receptor then being measured. A reduction in the tracer binding would be proof of psychoactivity of nitrous oxide. Only in this way can proof of direct psychoactivity in humans be obtained. I would recommend that the Home Office commission such research as a matter of urgency to settle this.”