by Dr. Joseph Mercola, Mercola:
- Die Welt, a mainstream media outlet in Germany, revealed that numerous subjects who suffered adverse events, including deaths, during Pfizer’s COVID-19 shot trials were removed from the trial data
- A person known as “Pfizer subject C4591001 1162 11621327” died three days after receiving the second dose of Pfizer’s COVID shot, reportedly due to stroke and arteriosclerosis; it was deemed unrelated to the shots
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- The CDC has since warned that people ages 65 and older who received Pfizer’s updated (bivalent) COVID-19 booster shot may be at increased risk of stroke
- Die Welt also revealed contradictions in Pfizer documents, adverse events from the shot downplayed and mass unblinding of study subjects, which wasn’t revealed in a later approval study
- In November 2020, Pfizer claimed their COVID-19 shot was 95% effective against COVID-19, but this was highly misleading and based on flawed methodology, including excluding people who got COVID-19 within 14 days after their first shot
- Pfizer has profited immensely despite the concerns, earning a record $100 billion in 2022, including $37.8 billion for its COVID-19 shots and $18.9 billion for its antiviral drug Paxlovid
Details continue to emerge about coverups and fraud that took place during Pfizer’s COVID-19 shot trials. Die Welt, a mainstream media outlet in Germany, revealed that numerous subjects who suffered adverse events, including deaths, were removed from the trial data.1,2
Meanwhile, trial data were manipulated “to create the illusion” the shot is 90% effective, for instance by excluding participants who got injected and developed COVID-19 within the next 14 days.3 Taken together, it leaves little doubt that COVID-19 shots cannot be trusted.
Deaths Occurred Within Days of Shots
The Die Welt report described several deaths that occurred shortly after the injections, but were excluded from the trial data. Among them was a person known as “Pfizer subject C4591001 1162 11621327.” The person, a 60-year-old man, died three days after receiving the second dose of Pfizer’s COVID shot, reportedly due to stroke4 and arteriosclerosis.
Independent journalist Igor Chudov detailed the case on Substack, noting that the man was discovered via a welfare check, and may have died within two days of the shot. Chudov reported:5
“According to the medical examiner, the probable cause of death was progression of atherosclerotic disease. Relevant tests were unknown. Autopsy results were not available at the time of this report.
In the opinion of the investigator, there was no reasonable possibility that the arteriosclerosis was related to the study intervention, concomitant medications, or clinical trial procedures, but rather it was related to suspected underlying disease. Pfizer concurred with the investigator’s causality assessment.”
However, it appears the medical examiner may have been unaware the man had received an experimental COVID-19 shot shortly before his death, and didn’t give the examination a closer look. Pfizer also neglected to request the medical examiner’s report to assess a potential link. Chudov continued:6
“They just took the police report’s word that he died of ‘arteriosclerosis,’ stated that Covid Vax cannot cause ‘arteriosclerosis,’ and ruled it ‘unrelated.’ The patient was buried and forgotten. If I may guess, the examiner’s diagnosis was not even accurate. The medications that the deceased took, indicate no ongoing, severe sclerotic disease.”
Pfizer Falsely Ruled Deaths Were Unrelated to Shots
Another subject in Pfizer’s trial also died 20 days after the shots. The death was ruled as due to a cardiac arrest. But pharmaceutical specialist Susanne Wagner told Die Welt:7
“According to the current state of science, these two cases would be assigned to the vaccination, especially since the U.S. health authority CDC is currently investigating strokes in vaccinated people and it is known. [Pfizer’s investigators] falsely ruled these deaths unrelated.”
Indeed, an announcement made by the U.S. Centers for Disease Control and Prevention and the Food and Drug Administration warned that people ages 65 and older who received Pfizer’s updated (bivalent) COVID-19 booster shot may be at increased risk of stroke.8
The CDC’s Vaccine Safety Datalink (VSD), which uses near real-time surveillance to track vaccine safety, flagged the potential safety issue, revealing that those 65 and over were more likely to have an ischemic stroke 21 days after receiving Pfizer’s bivalent COVID-19 shot compared to 22 to 44 days later.9
The FDA and CDC released the statement on a Friday night before a three-day weekend, “which is proof they wanted to bury it,” Dr. Meryl Nass, a board-certified internal medicine physician with special expertise in vaccine safety and vaccine mandates, said.10 Even Florida Surgeon General Dr. Joseph Ladapo tweeted about the odd timing:11,12
“What better time than a Friday afternoon for @CDCgov and @US_FDA to let Americans know that the mRNA shots they’ve been pushing may be causing strokes? Don’t worry, we’ll make sure the word gets out — just like we’ve been doing for months.”
Die Welt also revealed contradictions in Pfizer documents and mass unblinding of study subjects, which wasn’t revealed in a later approval study:13
“In one fell swoop, the test management said goodbye to 53 subjects on August 31, 2020. The test candidates were ‘unblinded,’ which means they were informed about their vaccination status, a process that the Pfizer study protocol expressly only provides for ‘in emergencies.’
But there is nothing about it in the approval study. In protocol documents that are available to WELT, and which are actually not intended for the public, those responsible get caught up in contradictions.”
Severe Adverse Reaction to Shots Brushed Off
Another example revealed by Die Welt involves trial participant Augusto Roux, a lawyer in Argentina. After receiving his second dose of Pfizer’s COVID-19 shot, he experienced shortness of breath and chest pain, and passed out. Within days, he visited a hospital for his symptoms, where he tested negative for COVID-19 but a CT scan showed fluid, or pericardial effusion, in Roux’s heart.
A physician noted in his chart, “Adverse reaction to the coronavirus vaccine (high probability).” Despite this connection and ongoing health problems, this adverse reaction was downplayed by Pfizer and listed as unrelated to the shots. According to Die Welt:14
“Over the next few months, Roux lost 14 kilos [30.8 pounds], he had liver problems, and his heart sometimes beat irregularly … The diagnosis for the symptoms after the second vaccination is very likely to be ‘pericarditis,’ inflammation of the heart. All of this fits exactly with a clinical picture that the Paul Ehrlich Institute also has in its list of ‘rare side effects’ for mRNA vaccines.
… His story, one might think, should appear in Pfizer’s pivotal study papers, but it doesn’t. The pharmaceutical company’s papers say Roux informed the research team that he was hospitalized with pneumonia on both sides, following the initial report, which was classified as an ‘adverse event of toxicity level 1.’
That could have nothing to do with the vaccine, the file goes on to say, it is probably a Covid infection. Not a word that Roux had tested negative for Corona in several PCR tests.”
Pfizer Created an ‘Illusion’ of Effectiveness
In November 2020, Pfizer claimed its COVID-19 shot was 95% effective against COVID-19, but this was highly misleading and based on flawed methodology.15 One trick used to get this misleadingly high efficacy figure is to ignore people who got COVID-19 within 14 days after their first shot.
In Pfizer’s trial, 37.2% of those who were tested for COVID-19 within 13 days of their first shot were positive — but not counted as such. How can this skew results? As explained on Substack’s “Where are the numbers,” a newsletter about the abuse of science and statistics:16