Tag: Big Pharma

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Industry’s FDA

It’s no secret that the FDA represents the interests of Big Food and Big Pharma – not consumers. Here is a small example of its allegiance to large corporations that we hadn’t noticed before. Unfortunately, many people still believe that if the FDA says something it must be true.

The following comes from the FDA page called “Questions and Answers on Monosodium glutamate (MSG)” found here: https://www.fda.gov/food/food-additives-petitions/questions-and-answers-monosodium-glutamate-msg accessed on 7/22/2020.

What is MSG?

The FDA says that monosodium glutamate (MSG) is the sodium salt of the common amino acid glutamic acid. Glutamic acid is naturally present in our bodies, and in many foods and food additives.

How is it made?

The FDA says that MSG occurs naturally in many foods, such as tomatoes and cheese. People around the world have eaten glutamate-rich foods throughout history. For example, a historical dish in the Asian community is a glutamate-rich seaweed broth. In 1908, a Japanese professor named Kikunae Ikeda was able to extract glutamate from this broth and determined that glutamate provided the savory taste to the soup. Professor Ikeda then filed a patent to produce MSG and commercial production started the following year.

What is MSG?

Mono (single) sodium glutamate in science-speak is glutamate tied to a sodium ion, just as monopotassium glutamate would be glutamate tied to a potassium ion. That’s the makeup of the mono sodium glutamate occurring naturally in our bodies. (Glutamate is rarely found “free,” but is ordinarily tied to an ion such as sodium or potassium.)

The monosodium glutamate that Ajinomoto is selling is made up of manufactured glutamate, the impurities that invariable accompany manufactured glutamate, and sodium.

How is it made?

MSG doesn’t occur naturally anywhere — it’s made – manufactured! The monosodium glutamate that Ajinomoto is selling is a product made in Ajinomoto’s plant in Eddyville Iowa where glutamate is produced by genetically modified bacteria that secrete glutamate through their cell walls, which is then mixed with sodium. (The process for manufacturing MSG has been patented, and as the process is improved over time new patents are awarded.)

Want to learn more about how the FDA cooperates with industry? You’ll find it in our just-out book, The Perfect Poison (available here), on the webpages of the Truth in Labeling Campaign, on Pinterest, in The toxicity/safety of processed free glutamic acid (MSG): A study in suppression of information, and in countless books such as White Wash by Carey Gillam, and Eating May Be Hazardous To Your Health – The Case Against Food Additives by J. Verrett and J. Carper.

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Who’s Kidding Who

According to the Brownstone Institute, “Experts are concerned that a memorandum of understanding between the Bill & Melinda Gates Foundation and the U.S. Food and Drug Administration could give Gates ‘undue influence’ over the agency’s regulatory decisions.”

The truth is that Big Food and Big Pharma have been calling the shots at the FDA since 1968 when then FDA Commissioner Ley testified before the Senate Select Committee on Nutrition and Health and presented evidence from four studies that, he alleged, demonstrated that MSG was safe. It was later disclosed that two of the studies Commissioner Ley cited were incomplete and two did not even exist.

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Industry’s FDA

It’s no secret that the FDA represents the interests of Big Food and Big Pharma – not consumers. Here is a small example of its allegiance to large corporations that we hadn’t noticed before. Unfortunately, many people still believe that if the FDA says something it must be true.

The following comes from the FDA page called “Questions and Answers on Monosodium glutamate (MSG)” found here: https://www.fda.gov/food/food-additives-petitions/questions-and-answers-monosodium-glutamate-msg accessed on 7/22/2020.

What is MSG?

The FDA says that monosodium glutamate (MSG) is the sodium salt of the common amino acid glutamic acid. Glutamic acid is naturally present in our bodies, and in many foods and food additives.

How is it made?

The FDA says that MSG occurs naturally in many foods, such as tomatoes and cheese. People around the world have eaten glutamate-rich foods throughout history. For example, a historical dish in the Asian community is a glutamate-rich seaweed broth. In 1908, a Japanese professor named Kikunae Ikeda was able to extract glutamate from this broth and determined that glutamate provided the savory taste to the soup. Professor Ikeda then filed a patent to produce MSG and commercial production started the following year.

What is MSG?

Mono (single) sodium glutamate in science-speak is glutamate tied to a sodium ion, just as monopotassium glutamate would be glutamate tied to a potassium ion. That’s the makeup of the mono sodium glutamate occurring naturally in our bodies. (Glutamate is rarely found “free,” but is ordinarily tied to an ion such as sodium or potassium.)

The monosodium glutamate that Ajinomoto is selling is made up of manufactured glutamate, the impurities that invariable accompany manufactured glutamate, and sodium.

How is it made?

MSG doesn’t occur naturally anywhere — it’s made – manufactured! The monosodium glutamate that Ajinomoto is selling is a product made in Ajinomoto’s plant in Eddyville Iowa where glutamate is produced by genetically modified bacteria that secrete glutamate through their cell walls, which is then mixed with sodium. (The process for manufacturing MSG has been patented, and as the process is improved over time new patents are awarded.)

Want to learn more about how the FDA cooperates with industry? You’ll find it in our just-out book, The Perfect Poison (available here), on the webpages of the Truth in Labeling Campaign, on Pinterest, in The toxicity/safety of processed free glutamic acid (MSG): A study in suppression of information, and in countless books such as White Wash by Carey Gillam, and Eating May Be Hazardous To Your Health – The Case Against Food Additives by J. Verrett and J. Carper.

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Have your say!

FDA Commissioner Dr. Robert Califf sits in front of a teleprompter on Feb. 23 holding his first virtual meeting with FDA employees.

FDA Commissioner Califf is looking for suggestions for staffing.  The Truth in Labeling Campaign tweeted that he should start by hiring someone who will oversee removing toxic chemicals from food.  Someone who doesn’t work for Big Food or Big Pharma.  Someone who will really do something.

Commissioner Califf’s twitter address is @DrCaliff_FDA.

Drop him a tweet to inspire the FDA to do something that will benefit consumers.  It’s @DrCaliff_FDA.

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‘Recycled FDA commissioner’ with Big Pharma ties, returns to head agency. But does it really matter?

Dr. Robert Califf, a prominent cardiologist with extensive clinical research experience and big ties to Big Pharma, who served as FDA commissioner during Obama’s final year in office has once again been appointed top boss at the FDA.

Califf, who was dubbed the “ultimate industry insider” in 2015, hasn’t changed much during the years since he last was tagged to run the FDA. He may have even improved on his Pharma connections.

The consumer group Public Citizen notes that after Califf left the FDA in 2017 he “revived his lucrative ties with FDA-regulated pharmaceutical companies, receiving consulting fees totaling tens of thousands of dollars…”

The group called for the Senate to reject “Biden’s recycled FDA commissioner pick.”

But they didn’t. Despite being close, 50 YEAs to 46 NAYs, Califf’s nomination was confirmed. But in the scheme of how things work at the FDA, does the name of the FDA head really matter?

Big Food and Big Pharma run the show at the FDA, with agents in place at every level saving the commissioner from making hard decisions – such as how to continue to claim that toxic MSG and its toxic manufactured free glutamate (MfG) are harmless. 

But thinking on the bright side, maybe the Senate confirmation hearings could be made to serve a different purpose. Perhaps someone could get those 46 Senators who voted against Califf to have the use of toxic glyphosate (Roundup) banned – or even just limited. Or, maybe they could order an investigation as to why the FDA continues to serve the glutamate industry and not have MfG banned from use in processed foods – or at least labeled.  Now that would really be something.

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Food for Thought

Who has more clout with the FDA?  Is it Big Food or Big Pharma?

The FDA requires this statement to appear on all direct-to-consumer drug advertising:

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.

But you won’t find a phone number dedicated to taking reports of negative side effects of food.

In the mid 1990s, when there was consumer pressure (and a lawsuit) on the FDA to identify and label MSG and its toxic manufactured free glutamate (MfG), one could report reactions to the FDA’s Adverse Reactions Monitoring System (ARMS) if you could figure out a way to reach them. But ARMS was eventually shut down, not because it was no longer receiving reports, but because “They” knew that MSG and MfG and aspartame and sulfites were harmless.