FDA and Pfizer Collusion
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 25 Minutes (2 videos) |
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In August of 2021, the Public Health and Medical Professionals for Transparency (PHMPT) field a Freedom of Information Act request with the FDA to obtain documents used in the Pfizer mRNA vaccine approval.
Pfizer then petitioned the FDA to block release of that information for 75 years!1 Obviously, pretty much everyone who cared about or could be hurt by that information would be dead by then.
Fortunately, a judge rejected that proposal, and the documents are starting to be released, and it's becoming clear why they wanted nobody to see them.
Dr. Wolf has organized a large team of volunteer health professionals, lawyers, scientists, and others to pour through the huge number of pages, as they are released, to analyze the information. So far, some of their findings are:
- The 'vaccine' mRNA ingredients were not manufactured in the United States (where they would be subject to scrutiny by the FDA and other U.S.-based overseers) but in Belgium and Germany, working with a Chinese partner organization.
- In one of the U.S. facilities that combined and packaged the ingredients from overseas, FDA inspectors repeatedly found mold and bacterial contaminants in the supposedly sterile preparation areas. The FDA also noted that Pfizer was not doing adequate testing of samples to check for toxic contaminants.
- Safety test reports were missing large amounts of pertinent data.
- Testing data shows evidence of sampling that could skew the results to show a lower incidence of certain conditions such as myocarditis.
- There were 1200 deaths at the beginning of the vaccination program. Pfizer is still not giving up information that could tell us what percentage of the people taking the 'vaccine' were affected.
- The results reported by Pfizer was sloppily categorized as to make drawing any valid conclusions next to impossible.
The FDA ignored all these problems (and probably more to be seen) when it granted approval without further investigation. These, and other findings, suggest that the FDA is ignoring its normal procedures to give Pfizer carte blanche approval, no matter what problems may be present.
1 For more details, see this Report.
Naomi Wolf's Web Site: dailyclout.io
