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The FDA was forced by a judge to release clinical data on the COVID vaccines back in January and so 55,000 pages of documents were just released. The FDA had originally wanted to hide the data for 75 years and release it in 2096 because, of course, the FDA is basically engaged in a criminal conspiracy. The COVID vaccines should never have been approved. This was obvious from the very beginning when animal trials were skipped in the Trump Administration’s ill-fated “Operation War Speed.” And now it’s undeniably true. We have the clinical data, and it’s horrific.
Hiding out in one appendix is the clinical data for Pfizer’s vaccine — which lists 1,291 adverse side effects in alphabetical order. Let’s give you just the bad things that can happen to people who took the Pfizer vaccine that start with the letter “a” to enjoy:
...
Why would the FDA approve a new vaccine when 15,000 people had serious disorders of the nervous system after taking it?
There’s simply no good reason.
Tell your friends and tell your family: the vaccination of children must stop immediately. The U.S. government has bought 50 million doses of this poison for children under the age of 5 pedning FDa approval and it must never be allowed to use them.
Call your elected representatives, call your senators, call everyone you know to put a stop to this today.
Do not allow anyone to jab a child with this stuff.
Please help us to crowdsource review of these Pfizer documents! As you read the various documents, please comment and include reference to the document in question.
This is one of the most productive things that you could do to help at this point.
On behalf of myself and many others, thank you in advance.
https://creativedestructionmedia.com/news/2022/03/04/pfizer-drops-deadly-side-effects-document-bomb-on-vaccine-consumers/?source=patrick.net
Will this help?
The Pfizer Documents
>42,000 Adverse Events in First 3 Months
Justin Smith
In August 27 last year, four days after the Pfizer covid-19 vaccine was approved for children 16 years and above, a group of doctors and scientists submitted a Freedom of Information Act Request.
The group, known as Public Health and Medical Professionals for Transparency (PHMPT), simply wanted access to the same data that was submitted to the Food and Drug Administration (FDA) for the approval of the Pfizer vaccine.
The FDA said it will need more than 75 years to process the request, because commercially sensitive data had to be redacted. The vaccines were developed using public money, from the USA and Germany. Most people seem to have forgotten about that. The public have not got their cut of the $65 billion projected profits from the vaccines. Only the deaths and adverse effects. However, let’s put that small issue aside for the moment.
The group of doctors (PHMPT) sued the FDA after the FDA quoted the lead time of 75 years. Thankfully, the judge agreed with the doctors and ordered the documents to be released more quickly. Recently the first batch of these documents was released.
Yesterday, Dr. John Campbell, published a video analysing these documents. While I am very grateful to Dr. Campbell for helping to bring this information to the public, it also has to be stated that Dr. Campbell has done his fair share of promoting the vaccines during the course of the pandemic. He trusted the companies involved and the authorities. This was a mistake on his behalf, especially considering the criminal fines that the companies involved had already received in the past for falsely marketing their products. Nonetheless, Dr. Campbell for the most part does seem to have had something of an awakening and I am happy about that. I recommend watching the video all the way through.
Of course, the corporate media are silent.
03/14/22
Pfizer, FDA Hid Data Showing Clinical Trials Failed, Says Former BlackRock Advisor
In an interview with Naomi Wolf, former BlackRock investment advisor Edward Dowd explained why Wall Street lost faith in Pfizer and Moderna stocks when Pfizer and the U.S. Food and Drug Administration tried to hide clinical trial data.
The US Food and Drug Administration (FDA) attempted to delay the release of Pfizer's COVID-19 vaccine safety data for 75 years despite approving the injection after only 108 days of safety review on December 11th, 2020.
The FDA originally said that they were prepared to release 500 pages per month in a response to the Freedom of Information (FOI) request filed on behalf of Public Health and Medical Professionals for Transparency (PHMPT) requesting the safety data.
Instead, in early January 2022, Federal Judge Mark Pittman ordered them to release 55,000 pages per month. They released 12,000 pages by the end of January.
Since then, PHMPT has posted all of the documents to their website. The latest drop happened on March 1st 2022 and shows alarming statistics.
One of the members of PHMPT, Dr. Aaron Kheriaty, tweeted a link to the documents and noted that an analysis would be coming soon. A few hours later, he again tweeted this time noting that oncologists will be busy in the coming years.
In a massive drop of the Clinical Overview, Table 59 shows the percentage of subjects reporting at least one adverse event following dose one, dose two and the control group (i.e. placebo). This table shows that the vaccinated suffered fever, chills and pain 13 times more than the placebo group.
In another document, the APPENDIX: List of Adverse Events of Special Interest (AESI) totals over eight pages in length. It’s a monstrosity of a list but a search for “death” yields neonatal death and sudden unexplained death.
I have reached out to PHMPT for an interview to discuss further analysis.
https://www.rebelnews.com/fda_dumps_55_000_pages_of_pfizer_safety_data_per_judges_order?source=patrick.net