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Originally posted by Sri Oracle
one of the online stores that I purchase vitamins from is asking for support to stop the AER bill that will supposedly allow lawmakers and the pharm.inc to limit or condemn sales of nutritional supplements that have even casual association to heart attack, stroke, etc.
Natural Product Insider
Do a google search for: aer bill supplements
The bill is being put forth as a "regulation on an underregulated industry". It allows user level feedback to later appear as warnings on labels and bans on products. It seems that it will place power in the hands of pharm.inc lobbyists to outlaw more natural remedies in favor of petroluem/synthetic concoctions.
Let me know your thoughts.
concerned shaman,
Sri Oracle
Umm..did you even READ the article you posted?
All the bill does is requires manufacturers to report any adverse effects, no different than drug companies are required to do. It does nothing to condemn, limit, or ban any product whatsoever.
Its passage WILL be used as guilt by association to further damage the reputation and public confidence in dietary supplements. It WILL be used by lawyers to mine the records of dietary supplement companies for records of ALL adverse events, serious or otherwise. It COULD be used nefariously by any parties interested in smudging the reputation of dietary supplements by reporting an association (but not a causal link) between a supplement and an adverse event. Let the witch hunt begin.
Bill Sardi, Knowledge of Health, Inc.
Originally posted by whitewave
Apparently none of you are familiar with codex alimentarius-a bill which has already passed and is now in the implementation stages. It has outlawed our access to dietary supplements except by prescription from a medical doctor (not naturopathic doctors). John Hammell from IAHF is spearheading the movement to repeal this repugnant legislation. You can access his site and learn all about this restriction to our rights to dietary supplements at www.IAHF.com. I've spent many hours talking to him and he is a committed, dedicated and passionate supporter of individual freedoms. IAHF stands for International Alliance for Health Freedom. If we join Canada and Mexico to become North America instead of 3 separate nations then we can expect to have the same access to dietary supplements that those 2 nations have. Some may see that as a good thing since so many Americans go to Mexico to get treatments that can't be gotten in the USA, however; as a nurse, I see and treat many of those returning from Mexico where there is little if any regulation on dosages, sterility, etc. It's not usually a pretty sight. Canada is a socialist nation and dietary supplements access is very limited and very regulated. It is very possible that we may wake up one day very soon and find that there is no more vitamins available on the shelves at wal-mart and the only way you can get them is with a prescription from your allopathically trained medical doctor who says you have an FDA approved need for them. In other words, no vitamin C unless you have a vitamin C deficiency as evidenced by scurvy. Vitamin C is not FDA approved for any other use. For those who think naturopathic remedies "don't work" and have no value except as an amusing old wives tale- please read Mosby's Handbook of Herbs and Natural Supplements. There are case studies cited under each herb listed stating the research done and results found regarding each herb. Many are being studied for their applications as antibiotics (having shown promise or previous results in that area), more efficient anti diabetic treatments than insulin. The list goes on but herbs are not "nonsense". They are a multibillion dollar industry for a reason and the pharmaceutical industry wants those multibillion dollars. This legislation ensures they'll get it while the herd is culled to a more manageable number.
In 1989, a large outbreak of a new, disabling, and in some cases deadly autoimmune illness called eosinophilia-myalgia syndrome (EMS) was traced to L-tryptophan. The bacterial culture used to synthesize tryptophan by a major Japanese manufacturer, Showa Denko KK, had recently been genetically engineered to increase tryptophan production; with the higher tryptophan concentration in the culture medium, the purification process had also been streamlined to reduce costs, and a purification step that used charcoal absorption to remove impurities had been omitted. This allowed another bacterial metabolite through the purification, resulting in the presence of an end-product contaminant responsible for the toxic effects. The FDA was unable to establish with certainty that this was the sole cause of the outbreak. Tryptophan was banned from sale in the US, and other countries followed suit.
Though it is indisputable that Showa Denko KK did produce and sell a contaminated batch of L-tryptophan, there are some concerns that the FDA's handling of this accident unfairly favoured the pharmaceutical industry and the new antidepressant Prozac if only because of its curiously fortuitous timing. The March 22, 1990 ban on public sale of L-tryptophan came only four days before the media announcement of Prozac on March 26, 1990 in Newsweek magazine
Originally posted by bsl4doc
Why are you afraid of there being a database charting supplements and their effects? Scared that mean old Mr. Science will show herbs can't cure much?
Mariella
Originally posted by DontTreadOnMe
Originally posted by bsl4doc
Why are you afraid of there being a database charting supplements and their effects? Scared that mean old Mr. Science will show herbs can't cure much?
Mariella
Mariella,
As you plan to practice medicine in Europe, and are studying it there, are you so sure you know what the Medical/Drug Industry is up to in America
As I'm sure you are aware, some countries in Europe have a far more flexible approach to alternative medical practices.
Some MD s in this country think chiropractors are quacks and charlatans.
It is in no way a stretch of the imagination to think that Big Drugs and Big Medicine not only want a portion of the HUGE supplements industry in America, they want to CONTROL it.
Originally posted by DontTreadOnMe
Or that the consumer/patient does NOT want yet another drug. I guess you don't get it that a LOT of people want to take their health care into their own hands and not rely on MSM. We want alternative choices and don't want the government to interfere.
We don't want or need the government of MSM telling us what is good for us :shk:
Original Article
If passed, the bill will require companies to include on their product labels an address or phone number through which consumers can report adverse events that they associate with their use of a supplement or OTC drug. These companies will be required to notify FDA of any serious AERs they receive within 15 business days.
I think that answer is for more doctors to treat patients as human beings rather than subjects.
Originally posted by bsl4doc
The last time important medical care was "in our hands", things like bloodletting and spirit possession were common...
Originally posted by whitewave
Hey BS Doc,
The site I posted was the home page for the FDA. If I've been "hooked into it" then I propose that you have been hooked by the FDA as well since you are not allowed to prescribe anything they have not approved. Also, they were not selling any books, tapes, videos, etc. on their site. Please get your facts straight before you speak condescendingly on subjects you obviously have not researched. By the way, why would big pharmaceutical companies want to pay billions to buy out the alternative therapies businesses when it would be much cheaper to buy legislation that will force the pesky beggars out for you?
Honey, I've been a critical care nurse for 16 years and I'm waaaaaayyyy past the time of being impressed with the title "Doctor". I've seen too many outright stupid ones and quite a few dangerous ones, not to mention the arrogant, megalomaniacal, thoughtless, callous ones. Since it's obvious you didn't check out the sites I referenced, your opinion is another among many of the uninformed, swaggering, belicose braggart types so common among your profession.
The loss of our access to dietary supplements and alternative (to allopathic) treatments is a serious issue and needs discussion and plans of action among serious minded lovers of freedom. We can pick up patranizing prattle anywhere. Thanks for playing. Next.
Originally posted by bsl4doc
I still don't see where people are getting the impression that their supplements are being taken away from them. You equate having a number to report side effects to taking supplements off the shelf? That's a bit moronic.
Pharmaceutical companies have spent billions of dollars trying to get Washington to regulate your dietary supplements like European governments do. So far, that effort has failed in America, in part because of a 1994 law called the Dietary Supplement Health and Education Act. Big Pharma and the medical establishment hate this Act, because it allows consumers some measure of freedom to buy the supplements they want. Americans like this freedom, however-- especially the health conscious Baby Boomers.
The largely government-run health care establishment, including the nominally private pharmaceutical companies, want government to control the dietary supplement industry-- so that only they can manufacture and distribute supplements. If that happens, as it already is happening in Europe, the supplements you now take will be available only by prescription and at a much higher cost-- if they are available at all. This alone is sufficient reason for Congress to oppose the unconstitutional, sovereignty-destroying CAFTA bill.