rich:

It looks like you were on the righttrack. Good for you

regards
michael barron

On Mon, Mar 1, 2010 at 10:06 PM, Rich Murray <[email protected]> wrote:

> Arthur Hull Hayes Jr. 1933-2010 approved aspartame July 1981 -- NY Times
> says, "...can sometimes cause cause incapacitating headaches and even
> seizures.": Rich Murray 2010.03.01
> http://rmforall.blogspot.com/2009_03_01_archive.htm
> Monday, March 1, 2010
> http://groups.yahoo.com/group/aspartameNM/message/1596
> _____________________________________________________
>
>
> http://www.nytimes.com/2010/03/01/health/policy/01hayes.html
>
> http://www.nytimes.com/2010/03/01/health/policy/01hayes.html?pagewanted=print
>
> March 1, 2010
> Arthur Hayes Jr., Who Led F.D.A. in Tylenol Case, Is Dead at 76
> By Dennis Hevesi
>
> Arthur Hayes Jr., who while leading the Food and Drug
> Administration during the Reagan administration helped calm
> consumer fears after a Tylenol poisoning case and, amid some
> controversy, approved the use of the artificial sweetener found
> in Equal and Nutrasweet, died Feb. 11 in Danbury, Conn.
> He was 76 and lived in Oxford, Conn.
>
> The cause was leukemia, his son, Arthur III, said.
>
> Dr. Hayes, a pharmacological researcher, was appointed
> commissioner of the F.D.A. by President Ronald Reagan
> in April 1981.
> He served until August 1983.
>
> The biggest crisis faced by the agency under Dr. Hayes was a
> nationwide alarm in 1982 caused by the deaths of seven people in the
> Chicago area who had taken Extra-Strength Tylenol capsules laced
> with cyanide.
> The case remains unsolved.
> Under Dr. Hayes's leadership, the government and the drug industry
> responded by developing the first federal regulations requiring
> tamper-resistant packaging for all over-the-counter drugs.
>
> In 1981, Dr. Hayes granted approval for the use of the sugar
> substitute aspartame in dry foods and as a tabletop sweetener.
> Research had found that aspartame was associated with high rates of
> cancers in rats that had been given large doses, starting at what would
> be the equivalent of four to five 20-ounce bottles of diet soda a day
> for a 150-pound person.
>
> Dr. Hayes insisted that there was no need for people to avoid the
> sweetener.
>
> Marketed as NutraSweet (when used as a food additive) and Equal
> (the tabletop version), aspartame is now also used in products like
> soft drinks, breakfast cereals, pudding mixes and gum.
> Research done after Dr. Hayes's time as commissioner indicated that
> aspartame can sometimes cause incapacitating headaches and even
> seizures.
>
> Arthur Hull Hayes Jr. was born in Highland Park, Mich.,
> on July 18, 1933, one of four children of Arthur and Florence Gruber
> Hayes.
> His father was president of CBS Radio.
>
> Dr. Hayes received his bachelor's degree in philosophy in 1955 from
> Santa Clara University and then went to Oxford as a Rhodes scholar,
> earning a degree in philosophy, politics and economics in 1957.
> He returned to the United States to study medicine and graduated
> from Cornell University Medical School in 1964.
> He served in the Army Medical Corps from 1965 to 1967.
>
> From 1967 to 1981, Dr. Hayes was an assistant professor of
>>
> medicine and pharmacology at Cornell.
> He later became director of clinical pharmacology at the
> Pennsylvania State University medical school.
> After leaving the F.D.A., he was dean of New York Medical College
> and, in 1986, was named president of E. M. Pharmaceuticals.
>
> Besides his son, Arthur, he is survived by his wife of 49 years,
> the former Barbara Anne Carey; two daughters, Lisa Hayes and
> Kathy Saracino; two sisters, Mary Ann Kelley and Florence Hayes;
> his brother, Joseph; and eight grandchildren.
> _____________________________________________________
>
>
> methanol (11% of aspartame), made by body into formaldehyde in
> many vulnerable tissues, causes modern diseases of civilization,
> summary of a century of research, Woodrow C Monte PhD,
> Medical Hypotheses journal: Rich Murray 2009.11.15
> http://rmforall.blogspot.com/2009_11_01_archive.htm
> Sunday, November 15, 2009
> http://groups.yahoo.com/group/aspartameNM/message/1589
>
>
> opportunities re BA Magnuson, GA Burdock et al., Aspartame
> Safety Evaluation 2007 Sept., Critical Reviews in Toxicology:
> Rich Murray 2008.07.11
> http://rmforall.blogspot.com/2008_07_01_archive.htm
> Friday, July 11, 2008
>
> [ This part of the Murray critique starts by quoting from the
> Magnuson review: ]
>
> Following the approval of aspartame, a formal objection was
> submitted to the FDA (FDA, 1981) questioning the conclusions
> from the rodent studies on aspartame conducted by Searle, and
> proposing that aspartame may have the potential to cause brain
> tumors in humans.
>
> This objection resulted in FDA staying the regulation approving the
> marketing of aspartame in 1975, and the establishment of a
> Public Board of Inquiry to reexamine the studies submitted
> by Searle to the FDA.
>
> Prior to the evaluation by the Board, the 15 studies submitted
> by Searle were thoroughly audited by the Universities Associated for
> Research and Education in Pathology, Inc. (UAREP)
> and by the FDA.
>
> The findings of the UAREP, the FDA, and the Public Board of Inquiry
> were considered and evaluated by the Commissioner of Food and
> Drugs, resulting in the issuance of the commissioner's Final Decision
> that at projected levels of consumption, aspartame would not pose a
> risk of brain damage and will not cause brain tumors
> (FDA docket, 75F-0355, 1981) (FDA, 1981).
>
> This decision resulted in FDA vacating the stay of the original 1974
> regulation.
>
> Objections to the of the use of aspartame were again filed with the
> FDA in 1983; however, the regulations approving the use of
> aspartame was not stayed following these objections, as the FDA
> stated that they failed to create sufficient doubt about the safety of
> aspartame.
>
> A response to the objections and a denial for a hearing was issued in
> 1984 by the Acting Commissioner of Food and Drugs
> (FDA docket 75F-0355 and 82F-0305)
> (FDA, 1984; Wurtman and Maher, 1987). "
>
> [ In fact the FDA brought suit against Searle for its radically biased,
> improper scientific studies.
>
> The industry won by persuading the FDA's two attorneys to let the
> legal process languish.
>
> Soon, the attorneys inexplicably found pleasant, prosperous futures
> in the industry's networks.
>
> Similar adroit exercises in corporate realpolitic were led by the CEO
> of Searle, none other than that modest American hero,
> Donald Rumsfeld, who used Reagan's victory to immediately
> manipulate the FDA's approval by a brand new Commissioner,
> Arthur Hull Hayes, in July, 1981, of aspartame in dry foods, and
> soon in beverages two years later, whereupon the fortunate
> Commissioner, troubled by hints of political corruption, found a
> gracious life with the industry's PR agency.
>
> Donald Rumsfeld CEO 1977-85 G.D. Searle & Co., got new
> President Reagan to prohibit FDA opposition to aspartame
> 1981.01.25, history by lawyer James S. Turner: Murray 2007.10.29
> http://groups.yahoo.com/group/aspartameNM/message/1483
>
> aspartame history Part 1/4 1964-1976: Gold: Murray 1999.11.06
> http://groups.yahoo.com/group/aspartameNM/message/53
>
> aspartame expose 96K Oct 1987 Part 1/3:
> Gregory Gordon, UPI reporter: Murray 2000.07.10
> http://groups.yahoo.com/group/aspartameNM/message/262
> http://www.dorway.com/upipart1.txt
>
> revolving door, Monsanto, FDA, EPA: NGIN: Murray 2002.12.23
> http://groups.yahoo.com/group/aspartameNM/message/928  ]
> _____________________________________________________
>
>
> Rich Murray, MA
> Boston University Graduate School 1967 psychology,
> BS MIT 1964, history and physics,
> 1943 Otowi Road, Santa Fe, New Mexico 87505
> 505-501-2298  [email protected]
>
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>
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> _____________________________________________________
>
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