Pharmacology and legal status of cannabidiol

Ann Ist Super Sanita. 2020 Jul-Sep;56(3):285-291. doi: 10.4415/ANN_20_03_06.

Abstract

Cannabidiol (CBD) is the second most abundant cannabinoid present in Cannabis sativa L. It is not associated with psychotropic activity and is capable to mitigate the psychotomimetic effects produced by tetrahydrocannabinol (THC). The latest cannabis decriminalization policies and the high applicability in therapeutic and technologic-industrial fields, have determined an exponential marketing growth of foods, cosmetics and in particularly medicinal products containing CBD, which are easily available for consumers. Most importantly, on 2018 United States Food and Drug Administration approved CBD oral solution with the trade name of Epidiolex® for the treatment of two rare and severe forms of epilepsy, "Lennox-Gastaut syndrome" and "Dravet syndrome", in pediatric patients. The aim of this review was to focus on pharmacology and on legal status of CBD, to highlight the lack of harmonization of international regulatory laws over the marketing authorization of CBD-based products.

Publication types

  • Review

MeSH terms

  • Anticonvulsants / therapeutic use
  • Biotransformation
  • Cannabidiol* / adverse effects
  • Cannabidiol* / pharmacology
  • Cannabidiol* / therapeutic use
  • Drug Interactions
  • Epilepsies, Myoclonic / drug therapy
  • European Union
  • Humans
  • Italy
  • Legislation, Drug / trends*
  • Lennox Gastaut Syndrome / drug therapy
  • Marketing
  • Molecular Structure
  • United States
  • United States Food and Drug Administration

Substances

  • Anticonvulsants
  • Cannabidiol