The mRNA vaccines were released globally in early 2021 with the slogan “safe and effective.” Unusually for a new class of medicine, they were soon recommended by public health authorities for pregnant women.
By late 2021, working-age women, including those who were pregnant, were being thrown out of employment for not agreeing to be injected. Those who took the mRNA vaccines did so based on trust in health authorities—the assumption being that they would not have been approved if the evidence was not absolutely clear. The role of regulatory agencies was to protect the public and, therefore, if they were approved, the “vaccines” were safe.
The report contains significant new information that had been suppressed by the TGA and by Pfizer itself. Much of this relates directly to the issue of safety in pregnancy and impacts on the fertility of women of childbearing age. The whole report is important, but four key data points stand out:
• The rapid decline in antibody and T cells in monkeys following the second dose • Biodistribution studies (previously released in 2021 through an FOI request in Japan) • Data on the impact of fertility outcomes for rats • Data on fetal abnormalities in rats
We focus on the last three items as, for the first point, it is enough to quote the report itself: “Antibodies and T cells in monkeys declined quickly over 5 weeks after the second dose of BNT162b2 (V9), raising concerns over long term immunity.”
This point indicates that the regulators should have anticipated the rapid decline in efficacy and must have known at the outset that the initial two-dose “course” was unlikely to confer lasting immunity and would, therefore, require multiple repeat doses. This expectation of failure was recently highlighted by Dr. Anthony Fauci, former director at the U.S. National Institute of Allergy and Infectious Diseases.
The study demonstrated that the vaccine will travel throughout the body after injection and is found not only at the injection site but in all organs tested, with a high concentration in the ovaries, liver, adrenal glands, and spleen. Authorities who assured vaccinated people in early 2021 that the vaccine stays in the arm were, as we have known for two years, lying.
In terms of the impact on fertility and fetal abnormalities, the report includes a study of 44 rats and describes two main metrics: the pre-implantation loss rate and the number of abnormalities per fetus (also expressed per litter). In both cases, the metrics were significantly higher for vaccinated rats than for unvaccinated rats.
Roughly speaking, the pre-implantation loss ratio compares the estimated number of fertilized ova and the ova implanted in the uterus. The table below is taken from the report itself and clearly shows the loss rate for vaccinated (BNT162b2) is more than double the unvaccinated control group.
In a case-control study, a doubling of pregnancy loss in the intervention group would represent a serious safety signal. Rather than take this seriously, the authors of the report then compared the outcomes to historical data on other rat populations, 27 studies of 568 rats, and ignored the outcome because other populations had recorded higher overall losses. This range is shown in the right-hand column as 2.6 percent to 13.8 percent. This analysis is alarming, as remaining below the highest previously recorded pregnancy loss levels in populations elsewhere is not a safe outcome when the intervention is also associated with double the harm of the control group.
A similar pattern is observed for fetal malformations with a higher abnormality rate in each of the 12 categories studied. Of the 11 categories where Pfizer confirmed that the data are correct, there are only two total abnormalities in the control group, versus 28 with the mRNA vaccine (BNT162b2). In the category that Pfizer labeled as unreliable (supernumerary lumbar ribs), there were three abnormalities in the control group and 12 in the vaccinated group.
As with the increased pregnancy losses, Pfizer simply ignored the trend and compared the results with historical data from other rat populations. This is very significant, as it is seen across every malformation category. The case-control nature of the study design is again ignored, in order to apparently hide the negative outcomes demonstrated.
Known unknowns and missing data
Despite the negative nature of these outcomes, the classification of this medicine as a vaccine appears to have precluded further animal trials. Historically, new medicines, especially in classes never used in humans before, would require a very rigorous assessment. Vaccines, however, have a lower burden of proof requirement than ordinary medicines. By classifying mRNA injections as “vaccines,” this ensured regulatory approval with significantly less stringent safety requirements, as the TGA itself noted.In fact, mRNA gene therapies function more like medicines than vaccines in that they modify the internal functioning of cells, rather than stimulating an immune response to the presence of an antigen. Labeling these gene therapy products as vaccines means that, as far as we are aware, even today no genotoxicity or carcinogenicity studies have been carried out.
This report, which was only released after an FOI request, is extremely disturbing, as it shows that authorities knew of major risks with mRNA COVID-19 vaccination while simultaneously assuring populations that it was safe. The fact that mainstream media has (as far as we are aware) completely ignored the newly released data should reinforce the need for caution when listening to the advice of public health messaging regarding COVID-19 vaccination.
Similarly, the concept of a two-dose “course” was inaccurate, as endless boosters would likely have been required given the rapid decline in antibodies and T cells observed in the monkeys.
Most importantly, the data do not in any way support the “safe” conclusion with respect to pregnancy; a conclusion of “dangerous” would be more accurate. The assurances of safety were, therefore, completely misleading given the data disclosures in the recent FOI release.
Regulatory authorities knew that animal studies showed major red flags regarding both pregnancy loss and fetal abnormalities, consistent with the systemic distribution of the mRNA they had been hiding from the public.
Even now, it is impossible to give these assurances, given the fact that important studies have not, to the best of our knowledge, been done.
Pfizer elected not to follow up the vast majority of pregnancies in the original human trials, despite high miscarriage rates in the minority they did follow. Given all of the problems with efficacy and safety, the administration of these products to women of childbearing age and administration to healthy pregnant women is high risk and not justified.
