Aspartame Poison Century

1256 Words3 Pages
bulb-icon

Recommended: Analysis of aspartame

Aspartame Poison Century

Thalidomide is 90 years of aspartame, a.k.a. NutraSweet, Finn, Zero Cal, and other trademarks. The text of the American researcher Barbara Alexander Mullarkey was aired on the Internet by Betty Martini and his original can be found in http://www.dorway.com. This is a free radical for the Portuguese, made by me, Beatriz Medina in July 1996.

Aspartame can be considered thalidomide 90s. With names NutraSweet, Finn ZeroCal and other trademarks, sweeteners with aspartame are extremely dangerous because they are present in todaparte in dietetic foods, supposedly healthy, and even children's vitamins, medicines, puddings, gelatin and softening the more innocent coffee.

It is also found in Diet Coke and other diet sodas. Aspartame is a neurotoxin, i.e., a drug that destroys the brain and nervous system. The molecule has three components: aspartic acid, phenylalanine and methanol. Has been shown that aspartic acid causes brain lesions in animal experiments.

The existing phenylalanine in aspartame is neurotoxic when isolated from other amino acids in proteins. Facilitates the occurrence of seizures and blocks the production of serotonin, which is one of the substances on the brain to regulate sleep. Low levels of serotonin, and insomnia, causing depression, anxiety, moodiness and even symptoms of paranoia.

Finally, methanol poisonous wood alcohol that has blinded and killed thousands of converts after ingestion of formaldehyde and formic acid (the main component of the venom of the sting of fire ants). Formaldehyde, a deadly neurotoxin that is stored in adipose tissue, particularly in the hips and thighs, is used to embalm corpses and violent is a carcinogen.

There are 92 documented symptom...

... middle of paper ...

... because of the existing tests in its application for approval of the product, but switched sides and was working closely with attorneys from Searle. The case died when the time ran out.

Until 1996, the FDA received over 10,000 complaints from consumers against NutraSweet. This corresponds to 80% of all complaints on food additives, but the FDA does nothing to alert the public, which assumes that a product advertised as healthy as it should be safe. Not the first time the FDA approved a drug harmful.

Researchers at the Massachusetts Institute of Technology (MIT) observed 80 people who suffered brain seizures after eating or drinking products with aspartame. The Community Nutrition Institute declared: "These 80 cases which fit the FDA definition of imminent risk to public health, which requires the FDA to immediately withdraw the product from the market."

Show More
Related

  • Nutrasweet, Equal, Spoonful And Equal Measure

    1485 Words  | 3 Pages

    Aspartame, or more commonly known as NutraSweet, Equal, Spoonful and Equal Measure; was discovered purely by chance in 1965 by a chemist named James M. Schlatter, who was testing an antacid drug (Prantini; 2014). The commercial industry believed that “a wonder product” had been discovered, which stood to revolutionise the food industry as an artificial sweetener. Aspartame is an artificial sweetener which is found in many of our foods and beverages universally. Aspartame is two-hundred times sweeter than sugar and is commonly used as a tabletop sweetener, a sweetener in prepared foods, diet foods or drinks, flavored waters, chewing gum, condiments and is even found in flavoring of medicines. It is found in majority of our food products marketed for weight control (Prantini; 2014). Aspartame has a sweeter taste in comparison to sugar, and therefore less of the sweetener can be used in food products in order to achieve the same level of sweetness as if sugar was used; which results in an individual consuming fewer calories and less sugar (American Cancer Society; 2014).

    Read More

  • THE FDA SHOULD BE REQUIRED TOREGULATE THE INGREDIENTSIN ENERGY DRINKS

    1777 Words  | 4 Pages

    Consuming energy drinks such as Red Bull, Monster and the 5- Hour Energy Shot, which contains caffeine and other additives, is dangerous to an individual’s health and in some cases fatal. Manufacturers of energy drinks claim consumption of their products will improve athletic performance, concentration and reaction time, as well increase basal metabolism. However, manufacturers’ of energy drinks add additional energy-enhancing ingredients such as glucose, taurine, guarana and ginseng. Each of those ingredients has numerous adverse side effects, see table 1 on page 8. Yet, energy drink manufacturers are not required to list the amount or type of additive used in their products. According to the Food and Drug administration (FDA), approval of the FDA is required in order to use additives in conventional foods. Dietary supplements, is considered by the FDA as generally recognizes safe by qualified experts therefore not considered a food additive. Unfortunately, the FDA need not approve adding them to conventional foods such as drinks. Consequently, manufacturers of energy drinks are taking advantages of this by labeling their products as “dietary supplements. “ Therefore, the Food and Drug Administration (FDA) should be in a position to regulate the ingredients added to energy drinks. In addition, the Federal Food, Drug, and Cosmetic Act (FFDCA), which regulates both dietary supplements and conventional foods does not require manufacturers of conventional foods to report serious adverse events (FDA, 2012).

    Read More

  • Stella Liebeck: Coffee and Frivolity

    1199 Words  | 3 Pages

    ...rthrate in infants are all over the packages. Most medicines list a whole plethora of possible side effects of the medication. Yet coffee cups to this day have no mention of the ramifications of spilled coffee. Maybe someday McDonald’s and other fast food chains will print on their cups “Can cause life threatening burns. Handle with care.”

    Read More

  • Regulating Dietary Supplements

    2092 Words  | 5 Pages

    With all the unregulated dietary supplements being sold and recommended, our health insurance costs will continue to rise. If the product causes severe side effects, it should no longer be permitted to be sold in stores. The only way to touch the minds of many people is to inform them of the dangers of consuming dietary supplements. Disposing of all incorrect information in product labeling and ingredient lists is important. People need to recognize the faults that plague many advertisements. In addition businesses should promote safe products instead of the harmful ones that they advocate for. The United States Congress should consider regulating dietary supplements to maintain safety. If people are aware of the many lies companies present, then dietary supplements will be one less problem to worry about.

    Read More

  • Arsenic

    3034 Words  | 7 Pages

    Schroeder, Henry A., M.D., 1974, The Poisons Around Us; Toxic Metals in Food, Air, and Water: Indiana University Press

    Read More

  • Aspartame

    1623 Words  | 4 Pages

    I have had friends who were having symptoms, had all kinds of tests and were taking all kinds of medications and when they stopped consuming Aspartame, the symptoms disappeared. Written by Lisa Zak Physician Credentialer University Pediatric Associates, Inc. Women & Children's Hospital of Buffalo:

    Read More

  • Forensic Toxicology Essay

    1530 Words  | 4 Pages

    In the past, poisoning was one of the most popular forms of murder. There are countless natural substances in the world that when ingested into the body in high doses, can become lethal to the human body. What made this form of murder so famous is that most poisons mimic common medical diseases, leading physicians to believe a victim died of natural causes (Ramsland, n.d.). Aside from murder, this forensic discipline is also essential for determining accidental deaths and suicides. As stated earlier, forensic toxicology is the examination of toxic substances in human tissues, organs, and body fluids that may have contributed or caused death to an individual (Tilstone, Savage, Clark,

    Read More

  • Investigating Factors Affecting the Heat of Combustion of Alcohols

    1809 Words  | 4 Pages

    Investigating Factors Affecting the Heat of Combustion of Alcohols PLANNING SECTION Introduction ------------ Alcohols are organic substances, and consist of Hydrogen, Oxygen and Carbon. All alcohols are toxic but the amount that can be tolerated by the human body varies for different alcohols. For example drinking small amounts of Methanol can lead to blindness and even death.

    Read More

  • Trial Procedure in the Movie A Civil Action

    778 Words  | 2 Pages

    Before the jury decides a verdict, the last step in the trial process is the closing arguments. There were no closing arguments because the parties had to settle on nine million dollars. They did this because the plaintiff’s attorneys went bankrupt due to this case and they couldn’t afford to invest any more money into the case. Beatrice Foods ended up being not liable for the deaths of children so they were allowed to leave the case. Due to this, only W.R. Grace had to settle with the plaintiff. Later on in 1988, Jan Schlichtmann brought this case to the EPA’s attention and the EPA decided to bring lawsuits against the companies. W.R. Grace and Beatrice Foods ended up having to pay for their huge mistake. They had to pay for the largest chemical cleanup in the Northeastern which cost sixty- four million dollars.

    Read More

  • Junk Science by Lee Ann Fisher Baron

    1609 Words  | 4 Pages

    In Lee Ann Fisher Baron’s “Junk Science,” she claims that the “food industry with the help of federal regulators” sometimes use “[a science that] bypasses [the] system of peer review. Presented directly to the public by…‘experts’ or ‘activists,’ often with little or no supporting evidence, this ‘junk science’ undermines the ability…[for] everyday consumers to make rational decisions” (921). Yet Americans still have a lot of faith in the U.S. Food and Drug Administration (FDA). According to a 2013 Pew Research study, 65% of Americans are “very favorable” or “mostly favorable” of the FDA. When it comes to what people put in their bodies, the FDA has a moral obligation to be truthful and transparent. The bottom line of the FDA’s myriad of responsibilities is to help protect the health of Americans. Deciding what to eat is a critical part of living healthily, and consumers must be able to trust that this massive government agency is informing them properly of the contents of food. While the FDA does an excellent job in many areas, it has flaws in other areas. One of its flaws is allowing the food industry to print food labels that are deceptive, unclear, or simply not true (known as misbranding). This is quite the hot topic because a Google search for “Should I trust food labels” returns well over 20 million results, many of which are blog posts from online writers begging their readers not to trust food labels. HowStuffWorks, a division of Discovery Communications, published an online article whose author claims that “[the food industry] will put what they want on labels. They know the game….” While the food industry is partially at blame for misbranding, the FDA is allowing it to happen. If a mother tells her children that it is oka...

    Read More

  • Thalidomide Research Paper

    1921 Words  | 4 Pages

    Thalidomide (α- phthalimido-glutarimide) was first marketed in Germany in 1956 as a sedative. In the following few years, it was prescribed in many countries in Europe, Asia, and Australia, to pregnant women in order to alleviate nausea and help them sleep [1]. However, it was banned in 1961 following an epidemic of malformations of the limbs, ears, and of internal organs. The negative effects of thalidomide led to the development of more structured drug regulations and control over drug use and development [1]. Despite its teratogenic effects, thalidomide has diverse pharmacologic properties and therapeutic potential in infectious, autoimmune, and many inflammatory conditions [2]. This paper will outline the current uses of thalidomide with

    Read More

  • The Poison of Physostigmine

    743 Words  | 2 Pages

    ...involuntary twitching of muscles. The mechanism underlying the toxic effects is that physostigmine targets the acetylcholinesterase and inhibits its activity, which inhibits the hydrolysis of acetylcholine, so increased acetylcholine will be useful to treat cholinergic disorders. Physostigmine, as a tertiary amine and can easily crosses blood-brain barrier. It is a soluble lipid and able to cross-placental barrier mainly by passive diffusion. It is rapidly absorbed from GI tract, subcutaneous tissues and metabolized largely destroyed in body.

    Read More

  • Thalidomide Research Paper

    1423 Words  | 3 Pages

    The continuous introduction of new drugs into the pharmaceutical world proves to have immense benefits to society’s treatment of medical issues, however it has also proved to cause disaster. A seamless example of the often terrible events that occur due to quickly advancing medicine is the disaster caused by the drug Thalidomide in the late 1950’s to the early 1960’s. Thalidomide was taken by thousands of pregnant mothers to battle symptoms of morning sickness. It is estimated that ten to twenty thousand babies were born with serious disabilities and physical defects due to this seemingly harmless drug. As researchers are finding new uses for the drug, controversy has arisen whether

    Read More

  • Persuasive Speech To Persuade People Not To Drink Energy Drinks?

    854 Words  | 2 Pages

    On the fox news program publish March 06, 2014 mentions how energy drinks effects the organs.

    Read More

  • Forensic Toxicology Essay

    943 Words  | 2 Pages

    Toxicology is the study of the adverse effects of chemicals on living organisms. Forensic toxicology takes it a step further, including a number of

    Read More

More about Aspartame Poison Century

Open Document