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Originally posted by boncho
reply to post by v1rtu0s0
FDA's actual position:
FDA's guidance documents, including this guidance, do not establish legally enforceable responsibilities. Instead, guidances describe the Agency's current thinking on a topic and should be viewed only as recommendations, unless specific regulatory or statutory requirements are cited. The use of the word should in Agency guidances means that something is suggested or recommended, but not required.
Source
Feel free to quote the part where the FDA bans all suppliments and tries to take over the world.
Originally posted by Openeye
reply to post by v1rtu0s0
Thanks for posting this.
I mean how can you ban things which are natural?
Originally posted by nickendres
I have no clue who the guy in the video is, but he's full of it. If the FDA is taking supplements off the market, there's a reason for it! And I am talking as a collegiate athlete who has taken supplements for almost 9 years. In my experince, the supplements getting taken off the market have literally been steroids under the guise of "pro-hormones", or the supplements combination is pure crap and the supplement company is completely lying about what's in it. And guess what, if they really do take fish oil off the market and other related supplements, guess what supplement companies will do? THEY WILL STILL PUT IT IN THEIR SUPPLEMENTS, the only difference will be instead of telling the consumer that they are buying fish oil, they will say something to the effect in the ingredients section Ultimate,Mega,Scare-Small-Children Proprietary Heart-Blend. "Hey bro, isn't it time you get your heart JACKED too! Take our product that now include our state of the art Ultimate,Mega,Scare-Small-Children Proprietary Heart-Blend" Even though it's really still Fish Oil. Open up your pantry and look at some of your food, I gaurantee at least one product will have "spices" as an ingredient. It's kinda like that.
Originally posted by v1rtu0s0
Originally posted by nickendres
I have no clue who the guy in the video is, but he's full of it. If the FDA is taking supplements off the market, there's a reason for it! And I am talking as a collegiate athlete who has taken supplements for almost 9 years. In my experince, the supplements getting taken off the market have literally been steroids under the guise of "pro-hormones", or the supplements combination is pure crap and the supplement company is completely lying about what's in it. And guess what, if they really do take fish oil off the market and other related supplements, guess what supplement companies will do? THEY WILL STILL PUT IT IN THEIR SUPPLEMENTS, the only difference will be instead of telling the consumer that they are buying fish oil, they will say something to the effect in the ingredients section Ultimate,Mega,Scare-Small-Children Proprietary Heart-Blend. "Hey bro, isn't it time you get your heart JACKED too! Take our product that now include our state of the art Ultimate,Mega,Scare-Small-Children Proprietary Heart-Blend" Even though it's really still Fish Oil. Open up your pantry and look at some of your food, I gaurantee at least one product will have "spices" as an ingredient. It's kinda like that.
I'm not even sure how to reply to this...
Why are you talking about legislation and law?
Originally posted by Jean Paul Zodeaux
Legislation is not law, merely evidence of law. If it is law, that legislation is protecting the rights of individuals, if the legislation is not doing that then it is merely legislation not rooted in law.
FDA's guidance documents, including this guidance, do not establish legally enforceable responsibilities. Instead, guidances describe the Agency's current thinking on a topic and should be viewed only as recommendations, unless specific regulatory or statutory requirements are cited. The use of the word should in Agency guidances means that something is suggested or recommended, but not required.
I don't know why people are talking about laws and legislation. This is neither.
There was a large tryptophan-related outbreak of eosinophilia-myalgia syndrome (EMS) in 1989, which caused 1,500 cases of permanent disability and at least thirty-seven deaths. Some epidemiological studies[41][42][43] traced the outbreak to L-tryptophan supplied by a Japanese manufacturer, Showa Denko KK.[44] It was further hypothesized that one or more trace impurities produced during the manufacture of tryptophan may have been responsible for the EMS outbreak.[45][46] The fact that the Showa Denko facility used genetically engineered bacteria to produce L-tryptophan gave rise to speculation that genetic engineering was responsible for such impurities.[47][48] However, the methodology used in the initial epidemiological studies has been criticized.[49][50] An alternative explanation for the 1989 EMS outbreak is that large doses of tryptophan produce metabolites that inhibit the normal degradation of histamine, and excess histamine in turn has been proposed to cause EMS.[51] Most tryptophan was banned from sale in the US in 1991, and other countries followed suit. Tryptophan from one manufacturer, of six, continued to be sold for manufacture of baby formulas. At the time of the ban, the FDA did not know, or did not indicate, that EMS was caused by a contaminated batch,[52][53] and yet, even when the contamination was discovered and the purification process fixed, the FDA maintained that L-tryptophan is unsafe. In February 2001, the FDA loosened the restrictions on marketing (though not on importation), but still expressed the following concern: