by Dr. Joseph Mercola 7/5/2022
Story at-a-glance • Pfizer classified almost all severe adverse events that occurred during its Phase 3 trials as unrelated to the injection. A 2,566-page document catalogues serious adverse events and six deaths during the trial. These events were all classified as “toxicity level 4,” which is the most serious, yet none of them was deemed related to the injection
• Examples of Level 4 adverse events — all of which were written off as “not related” to the mRNA injection — include acute respiratory failure, cardiac arrest, brain abscess, adrenal carcinoma (adrenal cancer) and chronic myeloid leukemia (blood and bone marrow cancer)
• Most Level 3 adverse events were also dismissed as unrelated to the shot. Only a small number were listed as related. Examples of Level 3 side effects include tachycardia (disruption of the normal electrical impulses that control your heart rate — the very problem that underlies most cases of “sudden adult death syndrome” or SADS) and ventricular arrhythmia (abnormal heart rhythm that makes the lower chambers twitch rather than pump — another underlying cause of SADS)
• A reanalysis of data from the Pfizer and Moderna COVID vaccine trials found that, combined, Pfizer and Moderna mRNA COVID-19 jabs were associated with a risk increase of serious adverse events of special interest of 12.5 per 10,000 vaccinated. Meanwhile, the risk reduction for COVID-19 hospitalization was only 2.3 per 10,000 participants for Pfizer and 6.4 per 10,000 for Moderna
• Whether intentional or not, mounting evidence now indicate the COVID-19 injections will result in depopulation through premature death and adverse effects on fertility in women and men alike. Research from Israel reveals the shot deteriorates sperm count and sperm motility in men for about three months post-jab
As the U.S. Food and Drug Administration continues to release Pfizer's clinical trial documentation,1 we're finding more and more evidence that very little has been done on the up-and-up, and the COVID jab trials may be among the most fraudulent in medical history.
Can All Serious Adverse Effects Be Written Off?Importantly, Pfizer classified almost all severe adverse events that occurred during its Phase 3 trials as unrelated to the injection. As reported by The Defender, June 21, 2022:2
"The latest release by the U.S. Food and Drug Administration (FDA) of Pfizer-BioNTech COVID-19 vaccine documents reveals numerous instances of participants who sustained severe adverse events during Phase 3 trials. Some of these participants withdrew from the trials, some were dropped and some died.
The 80,000-page document cache includes an extensive set of Case Report Forms (CRFs) from Pfizer Phase 3 trials conducted at various locations in the U.S., in addition to other documentation pertaining to participants in Pfizer-BioNTech vaccine trials in the U.S. and worldwide ...
A 2,566-page document4 catalogues the serious adverse events and six deaths that occurred during the trial. These events were all classified as "toxicity level 4," which is the most serious, yet none of them were deemed related to the injection.
This simply isn't believable. It's completely unrealistic, especially when serious events occur in multiple participants. A handful of examples of Level 4 adverse events listed in this document — all of which were written off as "not related" to the mRNA injection — include:5
• Acute respiratory failure
• Cardiac arrest
• Brain abscess
• Adrenal carcinoma (adrenal cancer)
• Chronic myeloid leukemia (blood and bone marrow cancer)
The six deaths reported were listed as being caused by arteriosclerosis, cardiac arrest, hemorrhagic stroke and myocardial infarction.6 Many participants also dropped out or were excluded from the trial due to serious side effects involving the heart, cardiovascular system, cancer, stroke, hemorrhage and neurological impacts.
Examples of Level 3 Adverse EventsMost Level 3 adverse events were also dismissed as unrelated to the shot. As reported by The Defender, only a "small number" were listed as being related to the injection. Examples of Level 3 side effects include:7
• Deafness/hearing loss
• Tachycardia (disruption of the normal electrical impulses that control your heart rate — the very problem that underlies most cases of "sudden adult death syndrome" or SADS)
• Ventricular arrhythmia (abnormal heart rhythm that makes the lower chambers twitch rather than pump — another underlying cause of SADS)
• Neutropenia (low neutrophil level in your blood; neutrophils are a type of white blood cell made by your bone marrow that fight infections by destroying viruses and bacteria)
• Vertigo
45% Experienced One or More Adverse EventsAnother document8 that raises suspicions of bias is one admitting that "40% to 45% of participants who received BNT162b1 and BNT162b2 across age groups and across dose levels reported one or more AEs [adverse events] from Dose 1 through 28 days (i.e., 1 month) after Dose 2."
BNT162b2 was the candidate injection that went on to receive Emergency Use Authorization (EUA) from the FDA. Among those who got the highest dose (30 micrograms) of BNT162b2, 50% of younger participants 25% in the older age group reported one or more adverse events.
More:
https://articles.mercola.com/sites/articles/archive/2022/07/05/covid-vaccine-adverse-effects.aspx
