The Food and Drug Administration had requested that it be granted at least 75 years to issue the full ‘redacted’ clinical trials data that Pfizer-BioNTech submitted to get its original Emergency Use Authorization in December 2020.
The judge in the case has now ordered the FDA to turn over the documents at a rate that is over a hundred times what it had requested.
“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!” Aaron Siri, who is the key litigator in the case, announced on his Substack page.
“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,” Siri continued.
The earlier court filing from the non-partisan Public Health and Medical Professionals for Transparency explained the need for urgent transparency.
“The FDA has proposed to produce 500 pages per month which, based on its calculated number of pages, would mean it would complete its production in nearly 55 years – the year 2076,” the court filing said. “Until the entire body of documents provided by Pfizer to the FDA are made available, an appropriate analysis by the independent scientists that are members of Plaintiff is not possible.”
“The entire purpose of the FOIA is to assure government transparency,” the plaintiffs argued. “It is difficult to imagine a greater need for transparency than immediate disclosure of the documents relied upon by the FDA to license a product that is now being mandated to over 100 million Americans under penalty of losing their careers, their income, their military service status, and far worse.”
The federal judge in the case has now issued a striking judgment against the FDA for attempting to cover up the clinical trials data at a pivotal time when the U.S. government and many states are claiming that we are presently in the middle of a pandemic-caused “emergency.” No.
Aaron Siri weighed in on the importance of the court’s ruling.
“No person should ever be coerced to engage in an unwanted medical procedure,” Siri said. ” And while it is bad enough the government violated this basic liberty right by mandating the Covid-19 vaccine, the government also wanted to hide the data by waiting to fully produce what it relied upon to license this product until almost every American alive today is dead. That form of governance is destructive to liberty and antithetical to the openness required in a democratic society.”
“In ordering the release of the documents in a timely manner, the Judge recognized that the release of this data is of paramount public importance and should be one of the FDA’s highest priorities,” he continued. “He then aptly quoted James Madison as saying a ‘popular Government, without popular information, or the means of acquiring it, is but a Prologue to a Farce or a Tragedy’ and John F. Kennedy as explaining that a ‘nation that is afraid to let its people judge the truth and falsehood in an open market is a nation that is afraid of its people’.”
The public transparency is critically important as news has surfaced that Pfizer buried the reporting of deaths in the placebo group prior to the “vaccine” authorization. And in November, a whistleblower came forward with revelations about how vaccine-maker Pfizer ‘falsified data’ and manipulated clinical trials.
Brook Jackson, a former clinical trial auditor who was fired after raising her concerns, came forward with inside information and documented evidence about Pfizer’s operations in a stunning BMJ investigation conducted by Paul Thacker. The disturbing report sends up red flags that the FDA and Pfizer were engaging in massive fraud against the American people to justify vaccine mandates.
Due to the federal judge’s order, however, there is at least some hope for transparency and for accountability for Big Pharma and the public health bureaucrats who perpetrated this massive fraud on the American people.