Page 3 - CANNABIDIOL (CBD) Critical Review Report Geneva, 4-7 June 2018 World Health Organization
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Cannabidiol (CBD)

                                                         Contents

                   Acknowledgements .................................................................................................................. 4

                   Summary................................................................................................................................... 5

                  1.     Substance identification ........................................................................................................ 6

                    A.   International Nonproprietary Name (INN) ............................................................................ 6
                    B.   Chemical Abstract Service (CAS) Registry Number .............................................................. 6
                    C.   Other Chemical Names .......................................................................................................... 6
                    D.  Trade Names .......................................................................................................................... 6
                    E.   Street Names........................................................................................................................... 6
                    F.   Physical Appearance.............................................................................................................. 6
                    G.  WHO Review History ............................................................................................................. 6

                  2.     Chemistry ............................................................................................................................... 6

                    A.   Chemical Name ...................................................................................................................... 6
                    B.   Chemical Structure................................................................................................................. 7
                    C.   Stereoisomers ......................................................................................................................... 7
                    D.  Methods and Ease of Illicit Manufacturing............................................................................ 7
                    E.   Chemical Properties............................................................................................................... 9
                    F.   Identification and Analysis ..................................................................................................... 9

                  3.     Ease of Convertibility Into Controlled Substances ............................................................ 10

                  4.     General Pharmacology........................................................................................................ 11

                    A.   Routes of administration and dosage ................................................................................... 11
                    B.   Pharmacokinetics ................................................................................................................. 11
                    C.   Pharmacodynamics .............................................................................................................. 12

                  5.     Toxicology............................................................................................................................ 13

                  6.     Adverse Reactions in Humans ............................................................................................ 13

                  7.     Dependence Potential .......................................................................................................... 14

                    A.   Animal Studies ...................................................................................................................... 14
                    B.   Human Studies...................................................................................................................... 14

                  8.     Abuse Potential.................................................................................................................... 14

                    A.   Animal Studies ...................................................................................................................... 14
                    B.   Human Studies...................................................................................................................... 14

                  9.     Therapeutic Applications and Extent of Therapeutic Use and Epidemiology of Medical

                         Use........................................................................................................................................ 15

                  10.    Listing on the WHO Model List of Essential Medicines.................................................... 18

                  11.    Marketing Authorizations (as a Medicinal Product) ......................................................... 18

                  12.    Industrial Use ...................................................................................................................... 19

                  13.    Non-Medical Use, Abuse and Dependence ........................................................................ 20

                  14.    Nature and Magnitude of Public Health Problems Related to Misuse, Abuse and

                         Dependence.......................................................................................................................... 20

                  15.    Licit Production, Consumption and International Trade .................................................. 20





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