https://www.youtube.com/watch?v=EWWvk2SaMS4. This is an extremly informative interview with Dr. Malone concerning the gross abuse of power and dissemination of misinformation by the FDA and CDC, the likely disastrous effect of the vaccine mandates, and related topics. All explained in a mild, soft voice. No histrionics or overt display of indignation. You have to listen carefully. But all the more devasating because of Dr. Malone’s unemotional tone.
Somehow this got past Youtube’s censors. I have no idea how. Best to access it quickly before it is taken down.
1
@EDGAR
The FOIA request was a the district level, Norhthern District of Texas, and the process is open to appeal. The reasons provided in the decision of the court cited that the burden on the FDA was outweighed by obvious urgency of the pandemic and a need to provide the American people evidence that the drug trials were not rushed (LOLOLOL) and the need to present the evidence prior to it becoming “stale”. Though these arguments are important and persuasive, I would not be surprised for this to not be the end of the legal challenges on this topic. The first drop is by January 31 with 12K pages and the first 55K page drop by March 1. The January date will likely go thru as the FDA had already agreed to it, but the March drop is another question altogether.
@PE LONI-
I figured that there would be 450.000 pages and with enough trained staff, they’d be read in a little over 8 months. Going more carefully we can assume a year but not longer.
I didn’t look at the video and don’t know what level Federal Judge made the ruling. Can it be possible that it may be appealed to higher courts. If so it can be stalled for years, unless expedition is granted. I know nothing much of American Law, better left to the Americans on this site.
The highlight of the report you put at the bottom of this page seems to indicate that it it a final decision.
Edgar there’s little difference between your position and the anti-vaxxers. There’s only one solution and that is to use the vaccine, make it available to all lands, along with science approved treatments.
@EDGAR
Sorry, my error. Yeah, this will be very rewarding I believe. We all owe Aaron Siri a great deal of thanks. The problem, however, with receiving 55K pages per month is that it will take someone dedicated enough to parse thru 55K pages per month to find all the choice details, which when I realize how long it took me to read that report on the autopsies which was only 56 pages, I am quite intimidated. Still, crowd sourcing works very well and I expect there will be a great deal to motivate the public within these pages. The FDA and Pfizer both wanted those records held til everyone on the planet was either dead or well into their seniority(75yrs from now). They weren’t hiding nothing, as we have already seen with the first report documenting several safety signals in Pfizer’s own records that were all ignored.
@PELONI-
I wasn’t really thinking of the courts. Like you say, I was thinking of a wide swell of the people’s demands on Government, and/or an FDA “relaxation”, of their “rules”.
@EDGAR
Well, we can hope, but I would not place too much faith in the courts regarding ordering these treatment be used, IMHO. On a case by case basis, with the family suing to use IVM, for instance, it is very much a mixed bag of success.
Personally, I don’t think the courts will ever come to the point of ordering such medicine to be used on a wide basis, ie for a city or a state or a nation. They do not feel knowledgeable enough to do so. If they did do so, a higher court would likely strike it down for that very same reason. It’s the white coat effect, and it is a powerful tool.
I personally believe that this will require a political remedy. As more and more nations, such as India and Japan, display the valid benefit of using treatments and achieving zero deaths it will eventually be too impossible for even the most vaccine addled supporter to ignore. Then it will require the public to demand their govts respond to the reality that their failed policy of no treatments are not achieving zero deaths, or anything remotely close to it, as wave after wave of the ill succumb to the illness.
This is why we are so lucky to have the benefit of Omicron. It will take time, and many will still die from Delta and her daughter variants, but Omicron will dominate and eventually the world will reach herd immunity. That is, unless they create new variants from Omicron due to a focused vaccine or due to a mutating treatment option such as Mulnipivar.
But I put no faith in the courts. Not even a little bit.
@PELONI-
A big victory indeed. An added result may be that the hitherto banned alterative medications which have long-proven successful use.. -like IVM and HCQ-, with be ordered, or allowed to be prescribed.
On behalf of a client, my firm requested that the FDA produce all the data submitted by Pfizer to license its Covid-19 vaccine. The FDA asked the Court for permission to only be required to produce at a rate of 500 pages per month, which would have taken over 75 years to produce all the documents.
I am pleased to report that a federal judge soundly rejected the FDA’s request and ordered the FDA to produce all the data at a clip of 55,000 pages per month!
This is a great win for transparency and removes one of the strangleholds federal “health” authorities have had on the data needed for independent scientists to offer solutions and address serious issues with the current vaccine program – issues which include waning immunity, variants evading vaccine immunity, and, as the CDC has confirmed, that the vaccines do not prevent transmission.
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https://www.youtube.com/watch?v=EWWvk2SaMS4. This is an extremly informative interview with Dr. Malone concerning the gross abuse of power and dissemination of misinformation by the FDA and CDC, the likely disastrous effect of the vaccine mandates, and related topics. All explained in a mild, soft voice. No histrionics or overt display of indignation. You have to listen carefully. But all the more devasating because of Dr. Malone’s unemotional tone.
Somehow this got past Youtube’s censors. I have no idea how. Best to access it quickly before it is taken down.
@EDGAR
The FOIA request was a the district level, Norhthern District of Texas, and the process is open to appeal. The reasons provided in the decision of the court cited that the burden on the FDA was outweighed by obvious urgency of the pandemic and a need to provide the American people evidence that the drug trials were not rushed (LOLOLOL) and the need to present the evidence prior to it becoming “stale”. Though these arguments are important and persuasive, I would not be surprised for this to not be the end of the legal challenges on this topic. The first drop is by January 31 with 12K pages and the first 55K page drop by March 1. The January date will likely go thru as the FDA had already agreed to it, but the March drop is another question altogether.
@PE LONI-
I figured that there would be 450.000 pages and with enough trained staff, they’d be read in a little over 8 months. Going more carefully we can assume a year but not longer.
I didn’t look at the video and don’t know what level Federal Judge made the ruling. Can it be possible that it may be appealed to higher courts. If so it can be stalled for years, unless expedition is granted. I know nothing much of American Law, better left to the Americans on this site.
The highlight of the report you put at the bottom of this page seems to indicate that it it a final decision.
Edgar there’s little difference between your position and the anti-vaxxers. There’s only one solution and that is to use the vaccine, make it available to all lands, along with science approved treatments.
@EDGAR
Sorry, my error. Yeah, this will be very rewarding I believe. We all owe Aaron Siri a great deal of thanks. The problem, however, with receiving 55K pages per month is that it will take someone dedicated enough to parse thru 55K pages per month to find all the choice details, which when I realize how long it took me to read that report on the autopsies which was only 56 pages, I am quite intimidated. Still, crowd sourcing works very well and I expect there will be a great deal to motivate the public within these pages. The FDA and Pfizer both wanted those records held til everyone on the planet was either dead or well into their seniority(75yrs from now). They weren’t hiding nothing, as we have already seen with the first report documenting several safety signals in Pfizer’s own records that were all ignored.
@PELONI-
I wasn’t really thinking of the courts. Like you say, I was thinking of a wide swell of the people’s demands on Government, and/or an FDA “relaxation”, of their “rules”.
@EDGAR
Well, we can hope, but I would not place too much faith in the courts regarding ordering these treatment be used, IMHO. On a case by case basis, with the family suing to use IVM, for instance, it is very much a mixed bag of success.
Personally, I don’t think the courts will ever come to the point of ordering such medicine to be used on a wide basis, ie for a city or a state or a nation. They do not feel knowledgeable enough to do so. If they did do so, a higher court would likely strike it down for that very same reason. It’s the white coat effect, and it is a powerful tool.
I personally believe that this will require a political remedy. As more and more nations, such as India and Japan, display the valid benefit of using treatments and achieving zero deaths it will eventually be too impossible for even the most vaccine addled supporter to ignore. Then it will require the public to demand their govts respond to the reality that their failed policy of no treatments are not achieving zero deaths, or anything remotely close to it, as wave after wave of the ill succumb to the illness.
This is why we are so lucky to have the benefit of Omicron. It will take time, and many will still die from Delta and her daughter variants, but Omicron will dominate and eventually the world will reach herd immunity. That is, unless they create new variants from Omicron due to a focused vaccine or due to a mutating treatment option such as Mulnipivar.
But I put no faith in the courts. Not even a little bit.
@PELONI-
A big victory indeed. An added result may be that the hitherto banned alterative medications which have long-proven successful use.. -like IVM and HCQ-, with be ordered, or allowed to be prescribed.
Big Win against PHARMA/FDA
INSTEAD OF FDA’S REQUESTED 500 PAGES PER MONTH, COURT ORDERS FDA TO PRODUCE PFIZER COVID-19 DATA AT RATE OF 55,000 PAGES PER MONTH!