Dr. Brownstein: The FDA Needs to be Replaced

At FDA.gov, it states, “FDA (U.S. Food and Drug Administration) is responsible for protecting the public health by assuring the safety, efficacy and security of human and veterinary drugs, biological products, medical devices, our nation’s food supply, cosmetics, and products that emit radiation.”

That sounds good to me. Too bad it is simply not true.

Two things have irritated me today. (And irritation is one of the things that causes me to start writing!)

The first, is a Medscape article that is headlined, “FDA Proposes Ban of Powdered Medical Gloves.” (Found at: http://www.medscape.com/viewarticle/860722?nlid=102645_3901&src=wnl_newsalrt_160321_MSCPEDIT&uac=83217PG&impID=1031379&faf=1)

The article states that after signaling its intentions for years, the US FDA unveiled a proposal to ban most powdered medical gloves to guard against multiple health threats to clinicians and patients. Surgical gloves were first used in the late 19^th Century and powder was used to make them easier to put on. However, all powders used have been found to cause problems in the patients exposed to them including the formation of adhesions and granulomas.

The FDA described the problems with powdered gloves in 1997. Over the next 19 years, many professional organizations such as the American College of Surgeons recommended that powdered gloves should be banned. During this time, the FDA received several citizen petitions recommending a ban against these gloves.

Jeffrey Shuren, M.D., director of the FDA’s Center for Devices and Radiological Health stated, “We take bans very seriously and only take this action when we feel it’s necessary to protect the public health.”

Here’s what I state: “GIVE ME A BREAK. WHERE WERE YOU FOR THE PAST 19 YEARS WHILE PATIENTS WERE SUFFERING AND YOU KNEW THERE WERE PROBLEMS WITH THESE GLOVES?”

19 years? Pathetic.

Irritation number 2:

In this case, the FDA, the same FDA asleep at the switch for 19 years in the story above, has decided to act quickly.

(Some of the following information came from Mike Adams at Natural News.com: http://www.naturalnews.com/053369_CBD_hemp_oil_extract_FDA_regulations.html)

The FDA has just launched a massive regulatory assault against cannabidiol (CBD) oil. CBD oil comes from marijuana and it many medicinal uses. I have successfully used medical marijuana (in the form of CBD oil) for many patients including those suffering with pain, seizures, autoimmune disorders and cancer.

Since CBD oil is a natural substance, you would think that the FDA could not ban it. However, in our crazy world, you would think wrong. So, how does the FDA move to ban the use of a natural substance?

It is easy. A drug company decided to research the benefits of CBD oil. This research triggered the FDA to consider CBD a substance to be ‘authorized for investigation as a new drug’ if it is the subject of an Investigational New Drug application (IND) that has gone into effect. You can read this for yourself here, under section 13: http://www.fda.gov/NewsEvents/PublicHealthFocus/ucm421168.htm#dietarysuppl

Folks, the FDA does not work for us. It works for Big Pharma. The FDA has started sending letters to companies manufacturing CBD oil informing them to stop producing and marketing it. Then, a Big Pharma company will come in and offer CBD oil for a price many times above what people are paying now.

If the FDA was working for us, the citizens, it would not wait 19 years to ban something that has been proven to be harmful. Nor would it allow the second most toxic chemical known to mankind—mercury—in any vaccine. For that matter, it would not allow neurotoxins such as aluminum and MSG in vaccines as well. However, that is for another story.

I hope the next U.S. President will address the failures at the FDA. These failures are mammoth and criminal. Folks, the FDA is beyond fixing. It needs to be replaced with a true agency that is looking out for our health.

DrB

Read the full article at DrBrownstein.com

Published on April 5, 2016

3 Comments

Harvey Marder April 19, 2016 at 11:53 am - Reply

Admin said:

At FDA.gov, it states, “FDA (U.S. Food and Drug Administration) is responsible for protecting the public health by assuring the safety, efficacy and security of human and veterinary drugs, biological products, medical devices, our nation’s food supply, cosmetics, and products that emit radiation.” That sounds good to me. Too bad it is simply not true. Folks, the FDA does not work for us. It works for Big Pharma. The FDA has started sending letters to companies manufacturing CBD oil informing them to stop producing and marketing it. Then, a Big Pharma company will come in and offer CBD oil for a price many times above what people are paying now. If the FDA was working for us, the citizens, it would not wait 19 years to ban something that has been proven to be harmful. Nor would it allow the second most toxic chemical known to mankind—mercury—in any vaccine. For that matter, it would not allow neurotoxins such as aluminum and MSG in vaccines as well. These failures are mammoth and criminal. Folks, the FDA is beyond fixing. It needs to be replaced with a true agency that is looking out for our health.

President Obama publicly declared war on Alzheimer’s disease in 2010.
That’s when he signed a bill called the National Alzheimer’s Project Act (NAPA) into law. That created a huge nationwide task force of scientists and researchers.
It involved millions in funding, and a green light for hundreds of new studies…
It was great PR for Obama. Bumped up his approval ratings for a little while.
But actually curing the disease? That was NEVER part of their plan.

BUT THEY DID CURE ALZHEIMERS
And the results they’re getting aren’t simply better than prescription drugs – they’re in a whole different league.
In fact, the stunning transformations have some doctors and researchers cautiously whispering the word “cure”…
• One patient – a 69-year-old business owner named Tom – was getting so bad he couldn’t remember the names and faces of the people who worked for him. But what really set off the alarm bells was when he read 6 chapters of a book… before he realized he had just finished that same book a week ago.
Brain scans showed clear evidence of Alzheimer’s disease. And things were getting rapidly worse.
But just a few short months of the ICT protocol completely reversed his symptoms. His memory snapped back to life. He could recall the name and face of everyone he worked with without a second thought.
Well, I’m afraid president Obama can’t let that happen.
Let me explain…

See, NAPA – like all Big Government’s “wars on disease” – was really just a handout to Big Pharma, plain and simple.
You see, by creating programs like NAPA, the government gets to control the flow of money used for research.
Then they funnel that money into research that they KNOW will never lead to a cure.
For Alzheimer’s disease, that means lots of studies on new prescription drugs, even though…
Billions of dollars and decades of research into prescription Alzheimer’s drugs have completely FAILED to slow the disease, let alone cure it!
Billions of dollars and decades of research into prescription Alzheimer’s drugs have completely FAILED to slow the disease, let alone cure it!

The FDA cant make any money on the cure for Alzheimers desease was discovered by NAPA IS FROM A HEALTH FOOD STORE THAT COSTS PENNIES ON THE DOLLAR AND CURES and reverses ALZHEIMERS DESEASE within 2 months back to normal and. THATS WHY THEY ARE TRYING TO FIND A PRESCRIPTION DRUG WITH SIDE EFFECTS THAT CAN LEAVE YOU LIFELESS and costs tens of thousands of dollars and thats why ALZHEIMERS ,CANCER,DIABETES, WILL NEVER BE CURED AND WILL ONLY SERVE AS A WAY THE GOV’T CAN FUNNEL TRILLIONS TO THE FDA FOR RESEARCH

TO CONTROL OUR DOCTORS,OUR GOVERNMENT,AND WALL STREET AND IN TURN CONTROL CONGRESS .

THE ICT protocol CURE : LITHIUM,VITAMIN E AND FLAXSEED OIL (NO SIDE EFFECTS)

(page 355 of treasuty of natural cures )
use low-dose lithium only (capsules or tablets containing 5 milligrams
of lithium from lithium aspartate or lithium orotate) is available from a
few natural food stores and compounding pharmacies, as well as from
the Tahoma Clinic Dispensary.
To be on the safe side,anyone taking lithium
also take a teaspoonful or two of flaxseed oil (or other essential fatty
acid), along with 400 IU vitamin E each day.
Lithium at high doses is dangerous for the heart so take 5 to 10 mg at the most availabe at health food stores but lithium over 30 megs is available only on prescription. aLL THIS COSTS ABOUT $35.00 FOR A MONTHS SUPPLY.

GO ALSO TO : pubmed.org and look up lithium

Abe April 14, 2016 at 8:58 pm - Reply

I think ‘d change the word replaced to prosecuted. I want to see some heads roll !!! They can start with Julie and go back and forward from there!!!

brad April 7, 2016 at 10:14 am - Reply

Admin said:
> At FDA.gov, it states, “FDA (U.S. Food and Drug Administration) is responsible for protecting the public health by assuring the safety, efficacy and security of human and veterinary drugs, biological products, medical devices, our nation’s food supply, cosmetics, and products that emit radiation.”
> 
> That sounds good to me.  Too bad it is simply not true.
> 
> Folks, the FDA does not work for us.  It works for Big Pharma.  The FDA has started sending letters to companies manufacturing CBD oil informing them to stop producing and marketing it.  Then, a Big Pharma company will come in and offer CBD oil for a price many times above what people are paying now.
> 
> If the FDA was working for us, the citizens, it would not wait 19 years to ban something that has been proven to be harmful.  Nor would it allow the second most toxic chemical known to mankind—mercury—in any vaccine.  For that matter, it would not allow neurotoxins such as aluminum and MSG in vaccines as well.
> 
> These failures are mammoth and criminal.  Folks, the FDA is beyond fixing.  It needs to be replaced with a true agency that is looking out for our health.

Rockefeller was instrumental in turning the UNITED STATES CHEMICAL AGENCY – kind of a chemical company chamber of commerce – into the FDA. 

This was about the time  he formed the AMA – whose LEADERSHIP elects it’s leadership. This is one reason why the AMA has such horrible and stupid “studies” like the one allegedly proving that taking “vitamin E” causes prostate cancer increases. What it REALLY showed is that FAKE vitamins don’t work, because the “vitamin E” they used in the study was dl-alpha tocopherol – the pharmaceutical drug.  The most effective i’ve  heard of that fake “E” acting was 70% as effective as real vitamin E. The worst i’ve heard about was zero vitamin effect – but it STILL blocked vitamin E receptors, preventing the uptake of vitamin E that would have actually helped your body. 

This is the same AMA which has lobbied congress for at least 2 yrs i know of to force mandatory adult vaccination on every legitimate adult resident of the USA – and they provided a really stupid excuse: they can’t get enough people for their vaccine studies…..

Every drug that was withdrawn from the market (such a benign, gentle word implying little danger, when they really needed to pull it because it was _____ing people UP!) because it was unsafe and inefffective had already been approved by the FDA because it was “proven safe and effective”.  (my adze) 

The 1958 FDCA – law of the land – states that ANY new product put into our food, drugs, or cosmetics IS LEGALLY DEFINED AS UNSAFE and MUST be PROVEN to be safe through extensive testing. WHICH HAS NEVER BEEN DONE  making ALL our GMOs totally illegal BECAUSE THE FDA BROKE THE LAW for any GMO in our foods – all over that garbage – our drugs – HPV and other really, really bad vaxxes – and probably in our cosmetics.

The FDA is a total lawbreaker – and WE DON’T NEED TO LABEL GMOs, WE JUST NEED TO HAVE “OUR” PREZ HAVE THE LAW UPHELD BY THE PSYCHO DRUG DEALERS IN FDA MGMT.