World Health Organization (WHO) Report CBD causes NO public Health Issue
Under the worldwide rising popularity as well as the controversy around Cannabidiol, popularly known as CBD, the World Health Organization has taken keen attention to it. WHO’s expert committee on Drug Dependence has recently conducted a thorough review of CBD and its uses. They have concluded that “CBD is generally well tolerated with a good safety profile”.
WHO officially recommended on December 14, 2017, that CBD should not be internationally scheduled as a controlled substance - which means – it should not be subject to strict international regulations, including its production and supply.
According to a critical review report published in June 2018, WHO says that “CBD is one of the naturally occurring cannabinoids found in cannabis plants” and “In humans, it exhibits no effects indicative of any abuse or dependence potential.”
The WHO team also commented about CBD’s efficacy in different clinical trials. They mentioned that CBD has shown the potential to be “an effective treatment for epilepsy in several clinical trials, with one pure CBD product (Epidiolex®). This research has completed its Phase III trials and is currently under review for approval in the U.S.”
WHO officially recommended on December 14, 2017, that CBD should not be internationally scheduled as a controlled substance - which means – it should not be subject to strict international regulations, including its production and supply.
According to a critical review report published in June 2018, WHO says that “CBD is one of the naturally occurring cannabinoids found in cannabis plants” and “In humans, it exhibits no effects indicative of any abuse or dependence potential.”
The WHO team also commented about CBD’s efficacy in different clinical trials. They mentioned that CBD has shown the potential to be “an effective treatment for epilepsy in several clinical trials, with one pure CBD product (Epidiolex®). This research has completed its Phase III trials and is currently under review for approval in the U.S.”