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On January 28, , the U. DEA listed it, along with nine other synthetic cathinones , on the Schedule 1 with a temporary ban, effective February 27, The President of the Republic of Italy classified cathinone and all structurally derived analogues including pyrovalerone analogues as Narcotics on January It is encompassed by those provisions, and therefore has been illegal for many years in New South Wales. The legislative action followed the death of two individuals from using it; one jumping off a balcony, another having a heart attack after a state of delirium. From Wikipedia, the free encyclopedia. For the pharmaceutical excipient called PVP, see polyvinylpyrrolidone. Anlage I Authorized scientific use only UK: Schedule I Illegal in: Society of Forensic Toxicologists. Archived from the original PDF on April 6, Journal of Mass Spectrometry. National Institute on Drug Abuse. Method development, drug distribution and interpretation of results'. Journal of Analytical Toxicology. Para-halogenated amphetamines and pyrovalerone cathinones'. A promising class of monoamine uptake inhibitors'. Journal of Medicinal Chemistry. Acquisition of self-administration and fixed ratio dose-response curves in rats. Retrieved 3 December Disposition of toxic drugs and chemicals in man. Retrieved September 29, China Food and Drug Administration. Retrieved 1 October The Sydney Morning Herald. Retrieved November 11, Retrieved 21 July Adapromine Amantadine Bromantane Memantine Rimantadine. Oxiracetam Phenylpiracetam Phenylpiracetam hydrazide. Retrieved from ' https: Designer drugs Norepinephrine-dopamine reuptake inhibitors Pyrrolidinophenones Stimulants. Views Read Edit View history. This page was last edited on 3 November , at By using this site, you agree to the Terms of Use and Privacy Policy.

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