Analysis by Dr. Joseph Mercola
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