FDA Gives Sole Herbal Product Rights to Big Pharma

Unbreakable

Bluelighter
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The FDA has taken a freely-available herbal product, sap of the dragon's blood tree, defined it as the drug Fulyzac, handed it to Big Pharma. Nature's gift is being polluted. What you get after Big Pharma and the FDA get their hands on it has lost much of its value and often been rendered into a poison, the very nature of a drug.

An extract from a South American tree known as dragon's blood is now classed as a drug and the FDA has handed sole rights to a single pharmaceutical corporation. The drug, which is made by Salix Pharmaceuticals, will be sold by Napo Pharmaceuticals of San Francisco under the brand name of Fulyzac. The generic term for it is crofelemer. It will be sold as a treatment for the diarrhea that's a common adverse effect of harsh HIV drugs.


The tree is botanically named Croton lechleri and called sangre de grado in Spanish and Portuguese, Long known to have several health benefits, extract from the tree is commonly available in health food stores around the world. This, though, is likely to change in the face of the FDA's action. It signals their role in facilitating Big Pharma's takeover of the natural world's largesse. Piece by piece, anything that holds any health value is being declared a drug. Exclusive rights to that drug are then handed over to a private corporation.

That's what happened to pregnenolone, a natural hormone that was routinely and inexpensively produced by compounding pharmacies, which provided it to pregnant women to prevent miscarriages.The FDA first targeted the compounding pharmacies, ordering them to stop producing it. Then, they handed exclusive rights to pregnenolone to a single corporation, which then turned around and raised the price 15,000 percent! That increase has taken it out of the reach of most women, making it available only to those of wealth or good insurance.

The name sangre de grado means dragon's blood. The trees are given that name for their red sap, as shown in the photo to the right. The sap has been used since time immemorial by residents of South America. As the photographer of the photo stated, it "seems to cure many things, including herpes simplex in my experience."

The sap of dragon's blood is traditionally used externally as a liquid bandage for wounds to staunch bleeding and promote healing. It's used internally for both stomach and intestinal ulcers. Other native uses include hemorrhoids, infected gums, skin disorders, and hemorrhage after childbirth.

Source:
http://www.disclose.tv/news/FDA_Gives_Sole_Herbal_Product_Rights_to_Big_Pharma/90918
 
well at least they can standardize it

the problem with herbal medicines is that the regulations make it so its not clear exactly what you're getting
 
I support the FDA here. It should be made in a GMP compliant facility, labelled properly, and full information should be disclosed in the form of a drug product abstract available to physicians and patients to determine if this drug is indicated, and for the patient to make fully informed consent to taking it.
 
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I support the FDA here. It should be made in a GMP compliant facility, labelled properly, and full information should be disclosed in the form of a drug product abstract should be available to physicians and patients to determine if this drug is indicated, and for the patient to make fully informed consent to taking it.
lol
 
Why lol?

You think stuff should be sold with no oversight on it's manufacture, and no standard of information regarding contraindications, side effects, effectiveness, and other results of clinical trials?

Cool, I think we should make chemo agents and radiotherapy devices available OTC too, then.
 
Can they really award exclusivity when it comes to a plant extract? There is a law that supposedly protects vendors from the DEA. From Wikipedia:

In the United States, a dietary supplement is defined under the Dietary Supplement Health and Education Act of 1994 (DSHEA) as a product that is intended to supplement the diet and contains any of the following dietary ingredients:

  • a vitamin
  • a mineral
  • an herb or other botanical (excluding tobacco)
  • an amino acid
  • a concentrate, metabolite, constituent, extract, or combination of any of the above
  • a substance historically used by humans to supplement the diet

Furthermore, it must also conform to the following criteria:

  • intended for ingestion in pill, capsule, tablet, powder or liquid form
  • not represented for use as a conventional food or as the sole item of a meal or diet
  • labeled as a "dietary supplement"

http://en.wikipedia.org/wiki/Dietary_supplement#Regulation
 
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