http://www.naturalnews.com/023175.html
(NaturalNews) In December of 1965, while James Schlatter, a chemist
for G.D. Searle & Company, was working on an anti-ulcer drug candidate
he accidentally discovered aspartame. He was recrystallizing aspartame
from ethanol when the mixture spilled onto the outside of the flask he
was using. Some of the powder landed on his fingers. Schlatter
discovered the sweet taste of aspartame when he absent-mindedly licked
his finger later. He realized that the sweet taste must have been the
aspartame.
G.D. Searle approached Dr. Harry Waisman (Biochemist, Professor of
Pediatrics, Director of the University of Wisconsin's Joseph P.
Kennedy Jr. Memorial Laboratory of Mental Retardation Research, and a
well-known expert in phenylalanine toxicity) in 1970 to research the
effects of aspartame on primates. The study began on January 15, 1970
and ended in late April, 1971. Dr. Waisman died unexpectedly in March,
of 1971.
In the study conducted by Dr. Waisman, seven infant monkeys were given
aspartame with milk. One died after 300 days. Five others experienced
grand mal seizures.
These actual research results were not included in the initial
application that G.D. Searle submitted to the FDA. G.D. Searle denied
knowledge of or involvement with anything involving this research
study. However, falsified results were submitted to the FDA bearing a
Searle Pathology-Toxicology project number. Dr. Waisman and G.D.
Searle both were responsible for the study design. Several false
statements were made by G.D. Searle, including that the animals
participating in the study were unavailable for autopsy after the
termination of the study.
Neuroscientist John W. Olney discovered that oral intake of glutamate,
aspartame and cysteine (all excitotoxic amino acids) cause brain
damage in mice. An internal G.D. Searle memorandum discussed the
strategy for getting aspartame approved.
In 1971, Ann Reynolds, a researcher who was employed by G.D. Searle,
confirmed aspartame's neurotoxicity in infant mice. Searle ignored her
discovery.
On July 26, 1974, the FDA approved aspartame for limited use. The
limited uses included free-flowing sugar substitute, tablets for
sweetening hot beverages, cereals, gum, and dry bases.
In August 1974 (before aspartame could go on the market) Dr. John
Olney, James Turner, and Label, Inc. (Legal Action for Buyers'
Education and Labeling) filed a formal objection stating that they
believed aspartame could cause brain damage, particularly in children.
On August 4, 1976, G.D. Searle representatives met with the FDA and
was successful in convincing them to allow G.D. Searle to hire a
private agency (University Associated for Education in Pathology
(UAREP) and pay them $500,000 to "validate" 12 other studies that
Searle had submitted to get aspartame approved by the FDA.
According to Arthur Hull Hayes, the FDA Commissioner during the early
1980s, the UAREP investigation was to "make sure that the studies were
actually conducted."
Dr. Kenneth Endicott, Director of UAREP, stated that the FDA had
"reasons to suspect" that Searle's tests "were not entirely honest."
Because the FDA doubted Searle's honesty, officials wanted UAREP "to
determine whether the re****ts were accurate."
In 1977, Donald Rumsfeld (a former member of the U.S. Congress and the
Chief of Staff in the Gerald Ford Administration) was hired as
President and CEO of G.D. Searle. Attorney James Turner, Esq. has
alleged that G.D. Searle hired Rumsfeld to facilitate the aspartame
approval difficulties that they were experiencing.
Rumsfeld's first action was to hire John Robson as Executive Vice
President. Robson was a former lawyer with Sidley and Austin (Searle's
Law Firm) and had also served as chairman of the Civil Aeronautics
Board (then connected with the Department of Trans****tation). Rumsfeld
also brought on Robert Shapiro as General Counsel. Shapiro had been
Robson's Special Assistant at the Department of Trans****tation.
Rumsfeld's next task was to hire William Greener, Jr., as Chief
Spokesman. Greener was a former spokesman in the Gerald Ford White
House.
At the time that Rumsfeld became President and CEO he was on the Board
of Directors of the Chicago Tribune. Shortly after Rumsfeld became CEO
of Searle he wrote an effusively positive article about the NutraSweet
Company.
On January 10, 1977, it was recommended to the U.S. Attorney that a
grand jury be set up to investigate G.D. Searle for violations of the
Federal Food, Drug, and Cosmetic Act, U.S.C. 331(e), and the False
Re****ts to the Government Act, 18 U.S.C. 1001. G.D. Searle and Company
and three of its responsible officers were investigated for willful
and knowing failure to make re****ts to the Food and Drug
Administration and for hiding pertinent facts and making false
statements in re****ts of the animal studies that were conducted to
establish the safety of the drug Aldactone and the food additive
Aspartame.
There were two studies where the violations committed by G.D. Searle
appeared to be especially grievous. The two studies investigated were
the previously mentioned 52-week toxicity study on infant monkeys
performed by Dr. Waisman (G.D. Searle withheld im****tant information
from the FDA) and a 46-week toxicity study of hamsters (G.D. Searle
had taken blood from healthy animals at the 26th week and claimed that
the tests had actually been performed at the 38th week). Apparently
many of the animals from this study were dead by the 38th week.
On January 26, 1977, G.D. Searle's law firm, Sidley & Austin,
requested a meeting with the U.S. Attorney prior to a grand jury
convening. A representative of Sidley & Austin who was present at that
meeting was Newton Minow (also on the Board of Directors at the
Chicago Tribune at that time).
On April 13, 1977, a memo from the U.S. Justice Department urged U.S.
Attorney Samuel Skinner to proceed quickly with the grand jury
investigations of G.D. Searle. The memo clearly shows that the Statute
of limitations on prosecution was going to expire soon (October 10,
1977 for the Waisman study and December 8, 1977 for the other study).
On July 1, 1977, U.S. Attorney Samuel Skinner left his U.S. Attorney
position to work for the G.D. Searle law firm of Sidley & Austin.
Thomas Sullivan became Samuel Skinner's successor. Assistant U.S.
Attorney William Conlon convened a grand jury, but he allowed the
Statute of Limitations to run out on the aspartame study charges.
Just over a year later, Conlon also accepted a job with G.D. Searle's
law firm, Sidley & Austin.
Robert McConnell was the Director of G.D. Searle's Department of
Pathology and Toxicology, the department that oversaw most of the
aspartame research. Mr. McConnell was specifically named in the
initial recommendation for investigation. According to McConnell's
attorney, his client was given a $15,000 bonus and it was requested he
take a 3-year sabbatical (he received $60,000 for each year). He was
deemed a "political liability."
In August 1977, the Bressler Re****t involving three key aspartame
studies (E5, E77/78 and E89) was released. Some of the findings from
these three studies reviewed by the Bressler-led FDA Task Force
included:
1. In one study, 98 of the 196 animals participating died but were not
autopsied until as much as one year later. Because of this delay, most
of the animal tissue could not be used. At least 20 animals had to be
excluded from postmortem examinations.
2. There was a discrepancy between the original pathology sheets and
the pathology sheets submitted to the FDA. There were differences
shown for 30 animals.
3. One animal was actually re****ted alive at week 88, dead between
weeks 92 and 104, and then alive again at week 108, and finally
permanently dead at week 112.
4. An outbreak of an infectious disease was not included in the re****t
to the FDA.
5. Tissue from some animals was noted to be unavailable for analysis
on the pathology sheets. However, the results from an analysis of this
"unavailable" tissue were submitted to the FDA.
6. There was evidence that the diet mix was not homogeneous (allowing
the animals to eat around the test substance). This evidence included
a picture as well as statements by a lab technician.
7. Fifteen fetuses from animals involved in one experiment were
missing.
8. Some sections from the animals were too thick for examination.
9. There was no do***entation about the age or source of the animals.
10. For one study, there was no protocol until it was well underway.
11. Animals were not adequately tagged to prevent mistakes.
12. Some laboratory methods were changed during the study but this was
not do***ented.
In March of 1979, the FDA was able to conclude that G.D. Searle's
aspartame studies were acceptable. They decided to convene the Public
Board of Inquiry (PBOI). This had been agreed to by Dr. John Olney and
Attorney James Turner over four years earlier.
In April of 1979, the FDA outlined the specific questions that were
going to be addressed by the PBOI. The scope of investigation was
limited to:
a. Whether the ingestion of aspartame (alone or together with
glutamate) poses a risk of contributing to mental retardation, brain
damage, or undesired effects on neuroendocrine regulatory systems.
b. Whether the ingestion of aspartame may induce brain neoplasms
(tumors) in rats.
Based on the answers to the above queries:
a. Should aspartame be allowed for use in foods or should the approval
of aspartame be withdrawn?
b. If aspartame is allowed for use in foods (if its approval is not
withdrawn) what conditions for use and labeling should be required, if
any?
In June of 1979, Acting FDA Commissioner Sherwin Gardner selected the
3-person Public Board of Inquiry (BOI). The selected panelists were
Peter J. Lampert, M.D. (Professor and Chairman, Department of
Pathology, University of California - San Diego), Vernon R. Young,
Ph.D. (University of Nutritional Biochemistry, M.I.T.) and Walle
Nauta, M.D., Ph.D. (Institute Professor, Department of Psychology and
Brain Science, M.I.T).
Dr. John Olney objected to the Commissioner's selection of Dr. Vernon
Young on grounds of both conflict of interest and lack of
qualifications.
Dr. Young had written articles in collaboration with G.D. Searle
scientists, though they were not aspartame related. Additionally, Dr.
Olney thought that the question of aspartic acid's neurotoxicity
needed to be examined by a neuropathologist and that Dr. Young was not
qualified because his field was Nutrition and Metabolism. Dr. Olney's
objections were overruled by the Acting FDA Commissioner. In the end,
Dr. Young was assigned to study the issue of aspartic acid toxicity.
One of the PBOI panelists, Dr. Walle Nauta, said, "It was a shocking
story we were told [about Searle's animal testing] but, there was no
way we could go after it. We had absolutely no way of knowing who was
right. We had to take the FDA's word."
On January 21, 1981, the day after Ronald Reagan became the 40th
President of the United States, G.D. Searle reapplied for the approval
of aspartame. G.D. Searle submitted new studies along with their
application. Reagan was expected to replace Jere Goyan, the FDA
Commissioner. G.D. Searle President & CEO, Donald Rumsfeld's
connections to the Republican Party were also thought to be connected
to Searle's decision to reapply for aspartame's approval at that time.
According to a former G.D. Searle salesperson, Donald Rumsfeld told
his sales force that, if necessary, "he would call in all his markers
and that no matter what, he would see to it that aspartame would be
approved that year."
Meanwhile, there were FDA scientists who were very concerned about
specific problems linking aspartame with brain tumors, brain lesions,
and general brain chemistry. Another concerned neuroscientist, Dr.
John Olney studied aspartame extensively and he expressed his concern
about the serious negative health effects aspartame consumption had on
the human body.
The concerns of these top scientists were of no consequence to
Rumsfeld. Rumsfeld made the decision to solve this problem politically
– not scientifically.
On October 15, 1982, G.D. Searle petitioned the FDA for approval of
aspartame use in soft drinks and children's vitamins.
On October 1, 1982 an amendment was attached to the Orphan Drug Act.
This act encourages the development of drugs for rare diseases. The
amendment extended the patent on one product -- aspartame -- by 5
years, 10 months and 17 days. The amendment did not mention aspartame
or G.D. Searle specifically and there was no debate or discussion on
this amendment.
This amendment was proposed by Senator Howell Heflin, brought up for
vote by Senator Robert Byrd, and pushed through by Representatives
Henry Waxman and Orrin Hatch. G.D. Searle requested Senator Heflin
sponsor the amendment. Heflin re****tedly received $9,000 in campaign
donations from G.D. Searle company executives shortly after this
amendment was approved. Senator Byrd received a $1,000 campaign
contribution from the CEO of G.D. Searle (Rumsfeld) before the
amendment was proposed. Representative Waxman received a $1,500
campaign contribution from the soft drink political action committee.
Senator Hatch also received $2,500 from the soft drink political
action committee prior to his re-election and $1,000 each from Daniel
Searle, Wesley Dixon (Daniel Searle's brother-in-law), and William
Searle. Senator Hatch has blocked hearings looking into the safety of
aspartame many times.
In 1985, G.D. Searle was sold to the chemical company, Monsanto.
Monsanto then created the NutraSweet Company as a separate subsidiary
from G.D. Searle.
In 1992, NutraSweet signed agreements with the Coca-Cola and PepsiCo
stipulating that The NutraSweet Company was their preferred supplier
of aspartame. The patent for aspartame expired on December 14, 1992.
This opened up the market to other companies.
In light of all of this information, it is not at all surprising that
most health-conscious people now believe avoiding NutraSweet is a
prudent practice. At some future point, if a scientific consensus
finally concludes that aspartame puts most consumers at risk, it will
be much too late. The best thing is to eat safely now.
About the author
Jo Hartley
Wife, Mother of 8, and Grandmother of 2
Jo is a 40 year old home educator who has always gravitated toward a
natural approach to life. She enjoys learning as much as possible
about just about anything!
http://www.loftymatters.com
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