Withholding serious Covid-19 vaccine adverse event outcome information from the medical community, from authorized dispensers, and from all potential Covid-19 vaccine recipients
There are five (5) sets of documents/videos below. The third document article includes a link to a particularly interesting set of letters to the CDC and FDA’s CBER, from a California ICU MD physician and from her attorneys.
Documents 1 and 2 (below) are slide presentations by the U.S. CDC and by the U.S. FDA’s Center for Biologics and Research (CBER) to FDA heads on October 22, 2020, two months prior to the start of Covid-19 vaccinations here in the U.S.
Within each slide presentation is one slide which lists the possible serious adverse event outcomes known, as of October 22, 2020, to be associated with the Covid-19 vaccines. Since these presentations, the FDA has not provided either of these two Covid-19 serious adverse event outcome lists (hereafter: “FDA C-19VAE lists”) to the medical community, nor to authorized dispensers, nor to potential Covid-19 vaccine recipients.
Thus, most, if not practically all, doctors, dispensers, and allied healthcare personnel are not aware that the FDA fully expected the diseases in these lists to start being reported to the FDA and CDC following the start of Covid-19 vaccinations. Consequently, reporting of these serious Covid-19 vaccine adverse event outcomes to the FDA and CDC has been thwarted by the FDA.
1) Available here is the presentation by Tom Shimabukuro, MD, MPH, MBA of the CDC COVID-19 Vaccine Task Force, Vaccine Safety Team. Page/Slide 31 is titled, “Preliminary list of VAERS AEs of special interest”. AE signifies Adverse Event.
2) Available here is the presentation by Steve Andersen, PhD, MPP, who is the Director, Office of Biostatistics & Epidemiology, CBER. Page 17, known as “slide 16”, is the “FDA Safety Surveillance of COVID-19 Vaccines : DRAFT Working list of possible adverse event outcomes”. This CBER slide presentation has been the subject of the article, FDA knew COVID vaccines would lead to severe adverse events, sanitized info was given to people to prevent vaccine-hesitancy, which includes an interview of Dr. Bryan Ardis, who first uncovered this list.
These two lists are essentially the same, since multiple sclerosis (MS), optic neuritis (ON), chronic inflammatory demelinating polyneuropathy (CIDP), ataxia, and vaccine enhanced disease (also known as Antibody Dependent Enhancement, or ADE) are autoimmune diseases.
Since, as Dr. Ardis noted, there are eighty (80) autoimmune diseases, each of these FDA C-19VAE lists represents approximately one hundred and ten (110) possible serious adverse event outcomes, including “Death”, which were expected to start being reported to the CDC and FDA following the start of public vaccination.
The FDA’s failure to provide either of these lists to healthcare professionals, to authorized dispensers, and to potential Covid-19 vaccine recipients is a violation of the FDA’s disclosure requirements for vaccines administered under an EUA (Emergency Use Authorization of Medical Products and Related Authorities – See Appendix A. EUA Conditions of Authorization: Required vs. Discretionary).
If the medical community and, eventually, the general public were to be made fully aware of these FDA C-19VAE lists, the public narrative would be vastly different than it is at the moment, as the alleged Covid-19 “vaccines” would begin to lose all legitimacy and the public would start to think twice about having one of these alleged Covid-19 “vaccines” injected into their bodies. As we’ve witnessed during this “Plandemic”, fear can be a great motivator; but, in light of these FDA C-19VAE lists, fear would motivate people to not receive any of these jabs.
3) On 10/13/21, The Children’s Health Defense newsletter, The Defender published an article titled, Physician to FDA, CDC: In 20 Years of Practicing Medicine, ‘I’ve Never Witnessed So Many Vaccine-Related Injuries’, where California ICU MD physician, Dr Patricia Lee’s letter to the CBER/FDA and CDC specifies the vaccine-related injuries she’s seeing in her patients. Dr. Lee also apparently has no idea these FDA C-19VAE lists exist. The vaccine-related injuries Dr. Lee names are the same as those in the FDA C-19VAE lists.
To view Dr. Lee’s and her attorneys’ letters to the CBER/FDA and the CDC, go to the above article and, in the first paragraph, click on the “a letter” link (or click on it here), which will provide you the opportunity to download these letters or open them in Adobe Reader or in your browser. Note that the letters are addressed, in part, to Tom Shimabukuro of the CDC, who presented the Document 1) list above, which likely explains why, as of October 6, 2021, neither the CDC or CBER had responded to Dr. Lee’s inquiry.
Now, less than a month later, Dr. Patricia Lee’s attorney, Aaron Siri of Siri | Glimstad, has revealed eleven (11) more physicians who have come forward, from “…across the country attesting to serious harms from Covid-19 vaccines. …Worse, many of these physicians were injured by a Covid-19 vaccine themselves and despite being physicians, the physicians from whom these injured physicians sought treatment also typically dismissed their injuries.” These eleven physician declarations are included in the following communication from Aaron Siri:
One Brave ICU Physician Reporting Covid-19 Vaccine Injuries Leads to a Dozen More
Hospital physician assistants, nurse case managers, nurses (also the four in the link above), physical therapists, occupational therapists, and other hospital healthcare personnel are now coming forward as whistleblowers, many stating that it is now primarily the vaccinated, not the unvaccinated, who are presenting to hospital, but not with Covid-19 symptoms, but symptoms indicative of one or more apparently vaccine-induced diseases; and, although these whistleblowers apparently have no idea of the existence of the FDA C-19VAE lists, the diseases they name are those in those FDA C-19VAE lists.
We need to get these FDA C-19VAE lists into the hands of every physician and allied healthcare worker, across the U.S., and stop this nonsense that the vaccinated have to beware of the unvaccinated, when the truth is actually vice versa; and, it is the vaccinated who need to become aware of what they’ve done to themselves. Only then, will the physicians and allied healthcare workers who are still doubters begin to realize that the diseases they are witnessing in their vaccinated patients are the vaccine-associated diseases in these FDA lists.
(Fuellmich’s translations to German have been removed from this particular copy of the video)
Dr. Bryan Ardis uncovered the CBER FDA C-19VAE list of document 2) above; and, has been working full time to get this information out to the medical community and to the public.
The interviewer is international trial attorney Dr. Renier Fuellmich who is at the forefront, globally, of exposing the fraud that was, and still is, employed to perpetrate this Covid-19 “pandemic”. Dr. Fuellmich is licensed in Germany and California and owns a ranch in northern California. He has successfully sued large multinational corporations such as Deutsche Bank for financial fraud, Volkswagen for their recent emissions fraud, and is now suing the world’s largest shipping company.
The 2nd half of the video, starting at Time = 32:15, deals with the CBER FDA C-19VAE list of possible serious adverse event outcomes (of Document 2 above); and briefly discusses the tens of thousands of apparently vaccine-related deaths reported to the VAERS and to the CMS (Medicare/Medicaid) reporting systems.
At Time = 54:32, attorney Fuellmich asks, “Ah, again, um, it’s bizarre. What is this about? It’s never been about health. This is about genocide, isn’t it?” – To which Dr. Ardis responds, “That’s what it appears to me. Genocide through infertilizing and sterilizing the world and, then, of course, there’s been tons of deaths, also. It appears there’s been no respect for life, or humanity at all, for the individuals who have been putting this in place and these mandates.” (and more about why are we trusting the FDA with our lives).