Corporate Take Over of Medical Marijuana Begins

“The FDA just criminalized one of the most miraculous healing medicines in the world by handing it over to Big Pharma”

In a well coordinated move, just a week after GW Pharmaceuticals (GWPH) just received FDA approval of their synthetic drug Sativex, (as strain of Sativia w/ chemicals) to treat seizures, when the weed alone was curing it naturally and cheaply, the FDA lays down the hammer on Med. Marijuana growers.

A Weed, A WEED, cures cancer, and disallows remote mind control, so Big PHarma, in bed with the FDA simply are chemically synthesizing the weed that cures all, rebranding, patenting, and then claiming patent rights to the WEED!

Of course the new synthetic pill will never, ever CURE, because that would end a multi-billion dollar business, so change the cure with some added chemicals, file a patent, get your buds at FDA to ban natural curing marijuana, and viola…you just tapped into another huge market to make billions and billions and never,ever find the cure.

****

The FDA just outlawed CBDs and hemp oil extracts by claiming all plant molecules now belong exclusively to Big Pharma

(NaturalNews) Hemp oil extracts containing CBDs (cannibidiols) are such a threat to the pharmaceutical industry that the FDA is now invoking totally insane justifications for outlawing them.

CBDs are non-psychoactive compounds found naturally in hemp plants. They work so well as powerful natural medicine that people everywhere are realizing CBDs work better than pharmaceuticals for treating epilepsy, seizures, neurological disorders and other serious health conditions (including HIV infections).

So the FDA has just launched a massive regulatory assault against CBDs by invoking the most insane logic you’ve ever heard. Here’s how it goes:

1) CBDs work so well that drug companies are now investigating them to be approved by the FDA as medicines.

2) Because CBDs are being investigated by drug companies, the FDA has granted CBDs status as being “investigated as a new drug.” In the FDA’s own language from their website, “FDA considers a substance to be ‘authorized for investigation as a new drug’ if it is the subject of an Investigational New Drug application (IND) that has gone into effect.”

3) Because CBDs work so well and have been authorized for drug investigations, the FDA now OUTLAWS them being sold as dietary supplements. Per the FDA’s own website: “FDA has concluded that cannabidiol products are excluded from the dietary supplement definition under section 201(ff)(3)(B)(ii) of the FD&C Act. Under that provision, if a substance (such as cannabidiol) has been authorized for investigation as a new drug for which substantial clinical investigations have been instituted and for which the existence of such investigations has been made public, then products containing that substance are outside the definition of a dietary supplement.”

4) Now the FDA has begun sending warning letters to CBD makers, claiming they are in violation of FDA regulations because they are selling “adulterated products.” Adulterated with what, exactly? CBDs, of course! “The debate over hemp CBD’s legal status continues after FDA sent eight warning letters to manufacturers of CBD dietary supplement and food products earlier this month,” reports Nutritional Outlook. “The warning letters cite impermissible health claims used to market the products, as well as CBD’s invalid status as a dietary ingredient due to its presence in two drug applications currently under consideration.”

Cancer is BIIIIIIIIIIIIIIIIIG Business and is predicted by W.H.O. to increase 70% in just the next 14 years