|(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.
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The first report of the discovery of the artificial sweetener was in the Journal of the American Chemical Society. It stated:
“We wish to report another accidental discovery of an organic compound with a profound sucrose (table sugar) like taste… Preliminary tasting showed this compound to have a potency
of 100-200 times sucrose depending on concentration and on what other flavors are present and to be devoid of unpleasant aftertaste.”
G.D. Searle has spent the last 40 years aggressively and recklessly promoting their accidental discovery with total disregard to the evidence they have gathered that show how dangerous and toxic this chemical is to human beings.
As early as 1984, studies were performed that clearly indicated the toxicity of Nutrasweet (aspartame) to living organisms. In 1984, the State of Arizona completed studies showing that aspartame in carbonated beverages can break down into free methanol (among other things) in 99°F temperatures. Compare this to human beings’ average body temperature and we begin to see a problem.
On May 13, 1998, the University of Barcelona produced a study clearly showing that Aspartame was transformed into formaldehyde in the bodies of the living creatures, and that upon later examination the formaldehyde had spread throughout the vital organs of their bodies.
The chemical breakdown of Aspartame in the human body is as follows:
Methanol, from Aspartame, is released in the small intestine when it meets the enzyme chymotrypsin.
The methanol is then converted to formaldehyde. The formaldehyde is next converted to formic acid. Formic acid is toxic and is commonly used as an activator to strip epoxy and urethane coatings. Phenylalanine and aspartic acid (90% of Aspartame) are amino acids normally used in the synthesis of protoplasm when supplied by the foods eaten. When unaccompanied by other amino acids, they become neurotoxic.
The FDA has established at least 92 medical/health problems that have symptoms associated with Aspartame. These include abdominal pain, anxiety attacks, Arthritis, Asthma and asthmatic reactions, bloating, edema , blood sugar control problems, brain cancer, breathing difficulties, burning eyes or throat, burning urination, chest pains, chronic cough, chronic fatigue, confusion, death, depression, diarrhea, dizziness, excessive thirst or hunger, flushing of face, hair loss or thinning of hair, headaches/migraines, dizziness, hearing loss, heart palpitations, hives , hypertension, impotency and sexual problems, insomnia, irritability, joint pains, laryngitis, marked personality changes, memory loss, menstrual problems or changes, migraines and severe headaches, muscle spasms, nausea or vomiting, seizures and convulsions, slurring of speech, swallowing pain, tachycardia, tremors, tinnitus, vertigo, vision loss, and weight gain.
Aspartame disease mimics the symptoms and many times worsens the following diseases:
Fibromyalgia, Arthritis, Multiple Sclerosis, Parkinson’s Disease, Lupus, Diabetes, Epilepsy, Alzheimer’s Disease, birth defects, Chronic Fatigue Syndrome, Lymphoma, Lyme Disease, and Attention Deficit Disorder.
In September 2004, an affidavit was signed describing the third world studies and the health hazards of aspartame. These studies were conducted in 1983 and 1984 by the G.D. Searle Company and were translated to English from Spanish in 1984. The “double blind” studies showed irrefutable evidence that aspartame caused severe health problems and even death to the study group. According to the affidavit, the doctor directing the studies has not been seen since the approval of aspartame in 1984. The affidavit also describes how the affiant was directed by G.D. Searle officials to destroy all records of the studies (including filed notes and/or translations) possessed by the affiant. The affiant also described how the translations were forwarded to the G.D. Searle corporate offices in Illinois.
These studies were destroyed and kept from the public and from health investigators.
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 reports 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 Transportation). Rumsfeld also brought on Robert Shapiro as General Counsel. Shapiro had been Robson’s Special Assistant at the Department of Transportation. 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 Reports 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 reports to the Food and Drug Administration and for hiding pertinent facts and making false statements in reports 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 important 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.
In August 1977, the Bressler Report 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 reported 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 report 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 documentation 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 documented.
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 reportedly 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.
By: Jo Hartley
About the author
Source: NaturalNews.com, April 29 2008