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Nonostante la sicurezza degli integratori, FDA insiste sul regolamento - salute supremo NewsGrabs 15 gennaio 2012

Written By anfaku01 on Monday, April 2, 2012 | 8:53 AM

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America's Largest Database Confirms: No Deaths from Vitamins

The new 203-page annual report of the American Association of Poison Control Centers, published online here, shows zero deaths from multiple vitamins; zero deaths from any of the B vitamins; zero deaths from vitamins A, C, D, or E; and zero deaths from any other vitamin.

Additionally, there were no deaths whatsoever from any amino acid or dietary mineral supplement.

Three people died from non-supplement mineral poisoning: two from medical use of sodium and one from non-supplemental iron. On page 131, the AAPCC report specifically indicates that the iron fatality was not from a nutritional supplement.


USA: The FDA is closing in on supplements

More telling about the FDA’s strategy for more heavy-handed regulation is the statement that “If you look at the numbers of NDI submissions versus the number of supplements introduced to the market since 1994, it would appear there is a significant lag in compliance.” On its face, the marketplace has changed over the last seventeen years. But who is responsible for this 17-year lag in compliance?

The Dietary Supplement Health and Education Act of 1994 (DSHEA) required manufacturers to submit pre-market notification applications for supplements and new ingredients when there is a history of use or other evidence establishing that an ingredient is safe when used as directed. The FDA has 75 days to accept or reject the application. A non-decision by the FDA means that the Agency accepts the evidence and that the product has complied, is approved, and can be marketed to the consuming public. Alternatively, a formal petition for a review and FDA issuance of an order prescribing the conditions under which a new dietary ingredient can be used and reasonably be expected to be safe, with the FDA having to respond within 180 days, can be filed. Again, shouldn’t a non-decision on a petition be considered as final Agency approval? If the Agency does not issue a decision either way, or if it cannot find a decision that was issued over the previous seventeen years, has it been the industry or the FDA itself who has not been in compliance with DSHEA?

Apparently, the FDA believes that manufacturers and suppliers have not met the FDA’s own self-interpreted DSHEA burden of proof standard to show to the FDA that there is reasonable evidence that supplements and new ingredients in supplements are safe.

I wish the FDA were that efficient on pharmaceuticals...

Some more details on this story and an action link

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Food and Nutraceutical Regulations - Global Snapshot

Every system of regulation has its pros and cons. The labelling of health-related foods should be based on scientific evidence, always bearing in mind harmonisation with global international standards. There should be a harmonisation of food regulations around the world. Economic growth and urbanisation are not enough evidence of the future growth of nutraceuticals, health demographic trends also support these growth forecasts. Consumers are deeply concerned about how their health care is managed, administered and priced. As health care cost has become high the consumers are frustrated with the expensive disease-treatment approach predominant in modern medicine; the consumer is now seeking alternative beneficial products like dietary supplement, functional food and nutraceuticals.

With innovative delivery mechanism to facilitate the use of nutraceuticals amongst its target groups, the world market is expected to witness a gradual shift toward natural ingredients.

The article discusses several of the major food regulatory systems and compares them. It becomes obvious that there are huge national differences in how to treat foods and in particular healthy foods. The question is: If those laws are to be somehow brought closer to each other, which would be the model to follow? I believe such a model (for ideal food legislation) needs to be worked out, to balance the current attempts - such as Codex Alimentarius - to put in the international food laws that are written by the large corporations.


Can Western guidelines govern Eastern herbal traditions?

Other supporters of herbal medicine worry that the rules are too demanding and could ban some therapies on which people depend. Adam Smith, science and communications officer for the Alliance for Natural Health International (ANHI) in Dorking, United Kingdom, a non-governmental campaign group promoting the use of herbal medicines and other approaches to healthcare, fears that patients will lose out on some Asian medicines because they have not been used in Europe for the requisite 15 years, even though they have been consumed in East Asia for considerably longer.

ANHI also detects a perceived bias in the THMPD towards products developed in the West, which often contain just one herb. Traditional Asian products contain mixtures of several herbs — making it difficult, time consuming and expensive to meet the directive's requirement to identify and quantify the active botanical ingredients or other biological agents in a herbal product. “These technical assessments require expensive methods,” says Smith. “The cost burden is a problem, particularly for small businesses,” he adds.

Middleton agrees that conducting scientific analyses are “tough” — even for products containing just one herb...

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News grabs are now being collected in a different way and will appear on this site a a stream of articles, linked as I find them. There will no longer be the weekly post that you are used to, and I do not know yet how the weekly feedblitz email alert will turn out. You can always check back directly at the site, however and you might want to get the RSS feed for notifications. The address of the site:

http://www.newmediaexplorer.org/sepp

the RSS feed for newsgrabs will be
feed://feeds.feedburner.com/Robin-Good-Breaking-New-Media-News

and the RSS feed for "features", articles that are original to the site, is
feed://www.newmediaexplorer.org/sepp/index.xml

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Change is coming ... to this site, after eight years of activity. The layout will be different and there will be, in addition to articles I may write from time to time, a running feed that is continually updated, of stories I highlight here. I will be using a new tool for the collection of information. It is called Scoop it... you can check it out here

http://www.scoop.it/t/health-supreme

Scoopit.jpg

If you liked this collection of health news, you can subscribe to the RSS feed or you can get it directly by email every week.

To do so, you need to enter your email in the space provided at the top of the page at health supreme , top of right side column, and click "subscribe me" and watch for a confirmation email.

If you find a particularly interesting story somewhere else, please tell me about it.

You can email me at (sepp@lastrega.com).

You can also find me on facebook (facebook.com/hasslberger)
and on Twitter

If you are interested in more than just health, also check out my other site on physics, economy and new energy

More information out there...

There is a lot more information out there about natural health and pharmaceutical medicine that I cannot cover ... but fortunately other sources for this kind of information exist.

Dr Mercola has a good health blog
Mike Adams publishes Natural News.
In the UK we have the One Click Group.
The Dr Rath Foundation campaigns for a New Healthcare System.
Natural health and nutrition on La Leva di Archimede
Food, Agriculture and more on the Organic Consumers Association site.


The individual is supreme and finds the way through intuition

posted by Sepp Hasslberger on Sunday January 15 2012

URL of this article:
http://www.communicationagents.com/sepp/2012/01/15/despite_safety_of_supplements_fda_insists_on_regulation_health_supreme_newsgrabs_15_january_2012.htm

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These articles are brought to you strictly for educational and informational purposes. Be sure to consult your health practitioner of choice before utilizing any of the information to cure or mitigate disease. Any copyrighted material cited is used strictly in a non commercial way and in accordance with the "fair use" doctrine.

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