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Section 6: Afterword

AFTERWORD:

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The above 1932 painting (a large fresco on the North Wall of the Detroit Institute of Arts) by the great Mexican muralist, Diego Rivera, was controversial because some members of the Christian faith thought it was sacrilegious. They thought Rivera was making a mockery of the Nativity Scene—with the child representing baby Jesus, the mother (or nurse) being Mary, the doctor being Joseph, the animals representing the stable animals, and the three scientists in the background representing the three wise men.

Supporters of the painting (who tended to be more progressive, more liberal-minded citizens of Detroit) believed that Rivera was appropriately honoring the wonders of medical technology—in this case, specifically, the potential of vaccines to save Humanity from life-taking diseases. The offended Christians wanted the fresco to be destroyed; Rivera’s supporters insisted that it be saved.

Although Rivera, himself, said that he was simply honoring medical technology, it is conceivable that he was either surreptitiously or subconsciously and unknowingly also issuing a warning—that humans must remain humble and not fall into the hubristic trap of thinking their medical discoveries, and the discoverers themselves, represent the new divine “Saviors” of Humanity. In that regard, it is interesting to note that the five adults in the painting appear to be quite satisfied and convinced that they are doing the right thing, while only the young child seems to have doubts.

Incidentally, although Rivera is said to have modeled the child after the Lindbergh baby (who had curly blond hair), the child’s facial appearance resembles that of Rivera.

Rivera probably chose to place farm animals in the foreground for two reasons: they represent the animals used in the early development of vaccines (e.g., vaccines derived from cowpox, horsepox, and sheep), and they represent farm animals in the nativity scene.

The fresco was not destroyed. Ninety years later, this fresco may still be viewed on the north wall of the Detroit Institute of Arts, where it continues to provoke thoughts about vaccination.

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Above is another Rivera fresco (1932) in the Detroit Institute of Arts. It is based on Rivera’s tour of the Parke-Davis pharmaceutical plant in Detroit in 1932 and is believed to represent a tribute to the pharmaceutical industry. It is conceivable, however, that it, too, is intended by Rivera (intentionally, or otherwise), at least in part, to convey a warning—about the potential to become too single-minded, too trusting, and too unquestioning, regarding the wonders of the pharmaceutical industry and its new products. It is unclear whether the gentleman in the foreground is entering scientific data or adding up profits.

Incidentally, Parke-Davis was bought by Warner-Lambert in 1974 and Warner-Lambert is now a subsidiary of Pfizer Inc, which acquired Warner-Lambert in 2000.

Parents and physicians might want to take into account that: In 2021 Pfizer made nearly $37 billion in sales from its COVID vaccine. Pfizer’s overall revenues in 2021 doubled to $81.3 billion. Pfizer anticipates record revenues of $98-102 billion during 2022. In 2009, Pfizer was ordered to pay $2.3 billion for illegally promoting and making false claims about four of its drugs. That represents the largest health care fraud settlement in history,

In 2004 Pfizer pleaded guilty to two FDA violations (committed by the Warner-Lambert pharmaceutical company before Pfizer bought the company) and paid $430 million in a Department of Justice (DOJ) settlement—for illegally marketing the drug Neurontin for unapproved purposes, “even when scientific studies had shown it was not effective” for those purposes. It was concluded that the company had manipulated data and had misrepresented or suppressed negative findings regarding the drug’s effectiveness.

In 2021, lawyers who were concerned about the safety and actual efficacy of Pfizer’s COVID vaccine, filed a FOIA (Freedom of Information Act) request that would require the FDA (Federal Drug Administration) to release all of the data (a total of 451,000 pages obtained from Pfizer) that the FDA relied upon to grant licensure of Pfizer’s COVID vaccine. In response to this FOIA request, the FDA asked a federal judge for permission to make the public wait until the year 2096 (75 years) before all of these 451,000 pages would be released. The FDA was willing to release no more than 500 pages per month (500 x 12 months x 75 years = 450,000 pages).

In January 2022, a U.S. District Judge ordered the FDA to produce at least 55,000 pages per month, which means the entire 451,000 pages would be released over a period of 8.2 months, rather than 75 years.

Perhaps the U.S. District Judge was influenced by the fact that, after lawyers filed their FOIA request in 2021, a confidential report prepared by Pfizer “for internal use only” was eventually released to the public (in October 2021): The title of this confidential report was: CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021. 5.3.6 Cumulative Analysis of Post-Authorization Adverse Event Reports of PF-07302048 (BNT162B2) received through 28-FEB-2021 : Worldwide Safety Pfizer : Free Download, Borrow, and Streaming : Internet Archive

The above is a report of the number of deaths and other adverse events that were spontaneously and voluntarily reported to Pfizer during the first three months after their COVID vaccine was first made available. The vaccines were initially shipped around the world on December 1, 2020. Cumulatively, from December 1, 2020, through 28 February 2021 (3 months), there was a total of 42,086 case reports of individuals who had experienced adverse events associated with their vaccination (25,379 medically confirmed and 16,707 non-medically confirmed). These individuals reported a total of 158,893 events. Most cases (34,762) were received from United States (13,739), United Kingdom (13,404) Italy (2,578), Germany (1913), France (1506), Portugal (866) and Spain (756); the remaining 7,324 were distributed among 56 other countries.

Unfortunately, we do not know how many total people had received vaccination by February 28, 2021. (That information is apparently redacted.)

From December 1, 2020, through February 28, 2021, there were 1223 spontaneous reports of deaths in vaccinated people. No data were provided, however, as to the age distribution of these 1223 people. Of the 42,086 total cases of people with adverse events, 76.4% of the cases were known to be less than 65 years old, 23.6% were known to be over 65, most (39%) were in the 31-50 age group. So, in general, the reported cases were not primarily in the elderly.

Despite 1223 reports of vaccine-associated deaths, Pfizer concluded that: “The data do not reveal any novel safety concerns or risks requiring label changes and support a favorable benefit risk profile of the BNT162b2 vaccine.”

Their report did not provide any detailed information about the 1223 fatalities. There was no information as to whether these 1223 fatalities were even investigated to obtain further details. The report provided no details as to the age distribution of the 1223 fatalities, or whether it was determined how many of the 1223 fatalities could convincingly be attributed to the vaccine as the cause of death (as opposed to death being unrelated to the vaccination). No details were provided as to the timing of the deaths in relation to the date of the vaccination. No information was reported as to the presence, absence, or nature of co-morbidities in those people who died. No information was reported as to the primary cause of death in those who died. There was no mention in the report of Pfizer planning to collect any further details, like those just mentioned, or being asked by the FDA to eventually report such details. Apparently, neither the FDA nor Pfizer were interested in knowing these details. Pfizer’s only plan was to continue filing the spontaneously reported adverse events.

As mentioned earlier, no data were provided, regarding the total number of people who had been vaccinated as of February 28, 2021. That is, we have no idea what the denominator was for the 1223 fatalities reported. Also, since these data depended on spontaneous reporting (as opposed to mandatory reporting), we have no idea whether this number of 1223 represents 100% of those who died in association with being vaccinated, or only 1% of the actual fatalities associated with vaccination, or somewhere in-between. The report did not indicate any plans to determine the denominator or the extent to which the 1223 fatalities represented an under-reported number. The report did not mention any need to shift to a mandatory reporting system. Apparently neither the FDA nor Pfizer were interested in these details.

One would think that reports of 1223 fatalities within the first 2-3 months after roll-out of the vaccine would have raised alarm and prompted: a shift to mandatory reporting (including retrospective reporting, not just prospective reporting); further, detailed investigation of all reported fatalities; determination of the denominator (the total number of people vaccinated); and at least a temporary halt to the mass vaccination campaign, until the just-mentioned details could be collected and analyzed. But neither the FDA nor Pfizer saw any cause for concern; any reason to even temporarily halt the campaign; any reason to collect any further details about those who had died; or any reason to determine the extent to which the 1223 represented an under-reporting of reality. Apparently, neither the FDA nor Pfizer were interested in these details.

Here we are, 2.5 years after the roll-out of the vaccine, and the latest official total numbers of vaccine-related deaths and injuries (as of April 3, 2022, as reported by the EudraVigilance Database, the MHRA Yellow Card Scheme, and the VAERS database—in the EU, UK, and USA, respectively) are: 69,053 vaccine-related deaths and 10,997,085 vaccine-related injuries. Historically, it appears that vaccine-related deaths are under-reported—with perhaps as few as 3-10% being reported. If 69,053 reported deaths represents only 3-10% of the actual number of deaths, that would mean an actual number between 2,301,766 and 690,530.

Despite the above data, Pfizer, the FDA, the CDC, the NIH, the WHO, and the conventional news media have seen no cause for concern, no need to even report this “confidential report” to the public, no need to even collect accurate detailed information (retrospectively or prospectively). This information would not even be available today, were it not for the FOIA request.

The above track record of the Pfizer pharmaceutical company (and the FDA) raises the possibility that Diego Rivera may well have been sending prescient warnings with the two frescos he painted for the Detroit Institute of Arts—90 years ago.

ACKNOWLEDGEMENT: I would like to acknowledge the enormous contribution Dr. Geert Vanden Bossche has made to global understanding of the COVID situation. Much of my personal understanding of the COVID situation is based on his deep scientific insights. I would like to thank him for his review of this document and his helpful comments, regarding it.

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