Monday, April 17, 2023
Bad batches of Pfizer mRNA Vaccines?
A trio of Danish researchers led by high powered physician-investigator Peter Riis Hansen, Department of Cardiology, Copenhagen University Hospital-Herleve and Gentofe recently had a research letter published in peer reviewed journal European Journal of Clinical Investigation. Titled “Batch-dependent safety of the BNT162b2 mRNA COVID-19 vaccine,” the investigators found three groupings of Pfizer-BioNTech COVID-19 vaccination batches with low, medium and high rates of adverse events. According to TrialSite contributor Dr. David Wiseman, “Is this modRNA degradation or DNA contamination.” The findings may correspond to Sasha Latypova contributions to TrialSite concerning various levels of vaccine safety associated with batches.
Background
By November 2022, 701 million doses of the Pfizer-BioNTech vaccine are linked to 971,021 suspected adverse events (SAEs) in the European Union. The authors point out that “vaccine vials with individual doses are supplied in batches with stringent quality control to ensure batch and dose uniformity.” They noted that at the individual vaccine batch level, clinical data was never reported and that a scenario “highly unlikely” would be “batch-dependent variation in clinical efficacy and safety of authorized vaccines.” Yet the prospect of investigation into “batch dependent variation” was worthy of investigation, according to the authors. Hence the study, an investigation into SAEs between the different Pfizer-BioNTech batches administered across Denmark and its 5.8 million people from December 2020, to January 11, 2022. This inquiry was possible because all SAE cases are linked with corresponding vaccine batch labels reported to and classified by the Danish Medical Agency according to seriousness of SAE as well as numbers of Pfizer-BioNTech doses in individual vaccine batches registered by the Danish Serum Institute. This data is publicly available if requested.
The study
By linking individual SAES to the batch label(s) of Pfizer-BioNTech dose(s) administered by subject, the authors could report on SAEs at the batch level in Denmark.
They divided total number of SAEs associated by batch by the number of doses in the batch to obtain the rate of SAEs per 1000 doses. They could not apply conventional regression statistics due to the significant heterogenous aspect to the observed relationship between number of SAEs and Pfizer-BioNTech vaccine doses. Rather, the authors employed use of non-hierarchical cluster analysis and general linear model (GLM) test for differences in SAE rates between batches, with reporting conforming to the EQUATOR guidelines.
So, what did they find?
52 different BNT162b2 batches was associated with 7,835,280 doses administered to 3,748,215 persons (2340-814,320 doses per batch), and 43,496 SAEs were registered in 13,365 persons which came to 3.19 ± 0.03 (mean ± SEM) SAEs per person. “In each person, individual SAEs were associated with vaccine doses from 1.531 ± 0.004 batches resulting in a total of 66,587 SAEs distributed between the 52 batches.”
The authors had to further analyze 61,847 batch-identifiable SAEs because batch labels were not fully registered or even missing for a total of 7.11% of all Danish SAEs. Out of this analysis 14,509 (23.5%0 were classified as severe SAEs with 579 (0.9%) involving SAE-related deaths.
Vaccine-related SAEs per 1000 doses varies between batches which was an unexpected find for the Danish authors. They reported “2.32 (0.09–3.59) (median [interquartile range]) SAEs per 1000 doses, and significant heterogeneity (p < .0001) was observed in the relationship between numbers of SAEs per 1000 doses and numbers of doses in the individual batches.”
As Wiseman recently noted, the authors found three groupings of Pfizer-BioNTech COVID-19 vaccination batches with low, medium and high rates of adverse events. The authors noted:
“Compared to the rates of all SAEs, serious SAEs and SAE-related deaths per 1.000 doses were much less frequent and numbers of these SAEs per 1000 doses displayed considerably greater variability between batches, with lesser separation between the three trendlines.”
They further identified:
“The observed variation in SAE rates and seriousness between BTN162b2 vaccine batches in this nationwide study was contrary to the expected homogenous rate and distribution of SAEs between batches.”
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Big Pharma Is Coming for Your Food: All Eyes Should Be on Missouri
Two years ago, moms led a revolution. Many of us refused to accept an untested gene therapy “vaccine” rushed to market during unnecessary and prolonged Covid lockdowns. The years since have vindicated moms: Our concerns about adverse reactions and potentially life-altering complications are, unfortunately, proving to be true. Courageous patriots fought unethical vaccine mandates and drew attention to the lack of informed consent as pharmaceutical corporations experimented on the population at large.
What you might not have seen coming is that Big Pharma has a back door to mass distributing the vaccine: the food supply. Moms for America learned from industry sources that this month farmers and ranchers will begin using mRNA vaccines on cattle and pigs. From the mainstream media? Crickets.
Not everyone is accepting this unprecedented power grab. Brave legislators in Missouri are facing off against the agricultural lobbyists and big corporations. Missouri House Bill 1169 is a simple measure to require disclosure of gene therapy products in everything from food to cosmetics, including soap. This two-page bill would not ban anything. It simply requires that products we purchase to consume or apply to our bodies are appropriately labeled if they contain materials that can alter our genetic material.
The disclosure bill defines a “gene therapy” as “any product with any capacity to alter, interfere with, or otherwise act in any manner similar or equivalent to genes.” If these substances were not going into our food supply, why are the lobbyists pitching a fit? The level of outrage among agricultural associations and professional lobbyist groups suggests that this is a very big deal.
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Civil Society Group in Canada Intensifies Its Investigation Into COVID-19: Was Pandemic Convenient Excuse for Government Overreach?
Canada’s Nationwide Citizens Inquiry (NCI) continues a private, civic society investigation into the COVID-19 response organize and led by that country’s national government. Afterall, this is the country that initially had no real strategy for COVID-19 vaccination, depending on a deal with China’s CanSino Biologics, which ultimately failed miserably. Canada, traditionally a solid long-time partner of the United States surprisingly did not participate in Operation Warp Speed initiated by former President Donald Trump.
This week the group will continue to conduct hearings this time in Winnipeg this Thursday, April 13, 2023. A group of prominent expert witnesses will offer their point of view, analysis and testimony. The country’s majority political class used the pandemic has a means to tighten their grip on power.
For example, during the well-publicized trucker protests, persons who contributed financially to those grassroots, political protests in some cases had their bank accounts frozen. Prime Minister Justin Trudeau enacted the Canadian Emergencies Act, arguing it wasn’t overreach given the mounting crisis across the country. On the other hand, an alternative point of view suggests Trudeau’s actions caused a breakdown in government, and Civil Liberties groups have claimed the use of the Emergencies Act was an abuse of government power.
NCI is a Canada-wide citizen-led and citizen-funded initiative to investigate governments’ COVID-19 policies in a fair and impartial manner that is completely independent from government. Through questioning led by lawyers, individual Canadians and experts will present evidence under oath to Independent Commissioners. The first six days of hearings were held in Truro, NS and Toronto, ON.
These expert witnesses include:
Natalie Bjorklund Gordon – Geneticist and Epidemiologist
Stephen Theriault – Medical microbiologist
Jessica Rose – Expert on the VAERS data
Staff Sgt Rick Abott – Edmonton Police Officer
Jay Bhattacharya – Professor of Medicine at Stanford, co-author The Great Barrington Declaration
Jeffrey Tucker – Founder of the Brownstone Institute
Deanne McLeod – Medical Researcher
Charley Hooper – Researcher on Early Covid Treatment
The Winnipeg hearings, from 9:00 am to 5:00 pm Central, will be broadcast live on the NCI website and on the NCI Rumble Channel. Follow the NCI on social media:
https://twitter.com/Inquiry_Canada and https://www.facebook.com/NationalCitizensInquiry
The Winnipeg venue is Holiday Inn Winnipeg – Airport West, 2520 Portage Ave., Winnipeg, MB R3J 3T6 Ph. (204) 885-4478
The conference organizations report that due to limited space in the room, the public is asked to arrange for access through Eventbrite.
Members of the media are asked to provide identification to NCI volunteers on site to obtain access. Prior notification of attendance to press@nationalcitizensinquiry.ca will assist in assuring seating.
NCI spokesperson, Michelle Leduc Catlin, will be at the hearings and is a contact for assistance.
Other hearings are planned in other locations across this vast country to the north of the U.S.
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Also see my other blogs. Main ones below:
http://edwatch.blogspot.com (EDUCATION WATCH)
http://antigreen.blogspot.com (GREENIE WATCH)
http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH) Also here
http://australian-politics.blogspot.com (AUSTRALIAN POLITICS)
http://snorphty.blogspot.com (TONGUE-TIED)
https://immigwatch.blogspot.com (IMMIGRATION WATCH) Also here
https://awesternheart.blogspot.com (THE PSYCHOLOGIST)
http://jonjayray.com/blogall.html More blogs
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