In a new interview with German attorney Reiner Fuellmich investigative reporter Sonia Elijah reports that during the period between December, 2020 and February, 2021 Pfizer recorded more than 158,000 adverse events and 1,200 deaths amongst the recipients of the COVID-19 “vaccines” in its clinical trial.
In a new interview with German attorneys Reiner Fuellmich and Viviane Fischer investigative reporter Sonia Elijah offers an overview of the shocking details of Pfizer’s clinical trial data. Elijah—who has pored over the Pfizer COVID-19 “vaccine” clinical trial documents since December of 2021—notes many highly “alarming” outcomes from the trial; including the recording of 158,893 adverse events, 1,228 deaths, 9,440 adverse event reports with “outcomes unknown,” and 1,403 instances of cardiovascular adverse events; of which the median time to symptom onset was 24 hours post injection.
Elijah, who’s a former BBC researcher with a background in economics, begins her interview with Fuellmich by thanking the Public Health and Medical Professionals for Transparency (PHMPT)—a “nonprofit, made up of public health professionals, medical professionals, scientists, and journalists [that] exists solely to obtain and disseminate the data relied upon by the FDA to license COVID-19 vaccines.” As Elijah notes, PHMPT—led by the now-famous Dr. Peter McCullough—is responsible for the submission of the clinical trial documents to the public, as the organization had to sue the FDA in order to get the regulatory body to produce them. (The FDA originally wanted up to 75 years to release all of the documents.)
As for what’s described in the Pfizer trial documents, Elijah highlights numerous instances of what she deems as (at least) grossly negligent behavior. The investigative journal lists a litany of reasons for that being the case, including a staggering 158,893 adverse events recorded in just a three-month-long period (from December 1, 2020 through February 28, 2021), amounting to three adverse events per clinical trial participant. Elijah also notes there were so many adverse events amongst participants, in fact, that Pfizer needed to hire on an additional 600 full-time staff members—on top of the original 1,200—responsible for going through the reports.
In the same three-month-long period Pfizer also logged 1,228 deaths amongst its COVID-19 “vaccine” recipients. Despite the incredible number of deaths (and all of the other adverse events) known to Pfizer by February of 2021, however, Elijah notes that former Pfizer Chief Medical Officer Dr. Mace Rothenberg told the Washington Journal in April of 2021 that “no corners were cut” during the company’s COVID-19 “vaccine” trial; specifically noting that “there have been no deaths that have occurred directly as a result of the vaccine alone.”
Elijah notes that, amongst the numerous adverse events, Pfizer recorded a large number of cardiovascular serious adverse events amongst trial participants; including arrhythmia, cardiac failure, coronary artery disease, myocardial infarction, stress cardiomyopathy, etc. There were an incredible 1,403 of these events recorded during the trial, with the median time to symptom onset being less than 24 hours post “vaccination.” Elijah notes Pfizer also knew by the end of February, 2021 that 136 of these adverse event cases ended up being fatal.
The investigative reporter goes on to note that women were three times as likely to be affected by the adverse effects of Pfizer’s COVID-19 “vaccine.” In regard to anaphylaxis, women were more than eight times as likely to experience the serious allergic reaction versus men post injection. Elijah notes this statistically significant finding suggests “gender-specific vaccine safety risks.”
Elijah also notes that despite the fact that “pregnant women were never officially part of Pfizer’s pivotal clinical trials” there were still 270 pregnancies amongst female participants. Unbelievably, out of the 270 pregnancies, outcomes for 238 were not reported. Amongst those that were reported, there were 23 spontaneous abortions, as well as instances of intrauterine death.
The Case Report Forms (or CRFs) were also erroneous or anomalous according to Pfizer’s clinical data dump. Elijah specifically notes missing severe adverse event case numbers; missing barcodes on lab samples; and inaccurate data entry. One peculiar case Elijah notes is in regard to the way the protocol for investigating “potential COVID-19 related pneumonia” was executed; or rather, note executed. The journalist notes that these instances should’ve triggered participant visits by Pfizer clinical administrators, but did not.
Elijah goes on to note many other serious logistical and ethical issues with Pfizer’s COVID-19 “vaccine” trial, saying “what’s really alarming are literally the safety studies that were not done. [No] safety pharmacology studies were done. No genotoxicity studies were done. No carcinogenicity studies were done. And [this is] a novel treatment.” Pfizer’s clinical scientists also apparently never looked to see where in the body the spike proteins produced by the COVID-19 “vaccines” were going in the body. “So they do not know, and we have this on record… . They have no idea. Those studies have not been done.”
Feature image: Corona Investigative Committee via Right2Freedom
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