Daniel Horowitz
Over 10,000 categories of nearly 1.6 million adverse events – many of them serious and debilitating – brought to you by Pfizer!
You might not have heard it in the news, but in recent months, Pfizer’s pharmacovigilance documents requested by the European Union’s drug regulator, the European Medicines Agency, have been released. They show that Pfizer knew about a sickening level of injury early on. An August 2022 document shows that the company already had observed the following scope of vaccine injury:
- 508,351 individual case reports of adverse events containing 1,597,673 events;
- One-third of the AEs were classified as serious, well above the standard for safety signals usually pegged at 15%;
- Women reported AEs at three times the rate of men;
- 60% of cases were reported with either “outcome unknown” or “not recovered,” so many of the injuries were not transient;
Highest number of cases occurred in the 31-50 year age group, and 92% did not have any comorbidities, which makes it very likely it was the vaccine causing such widespread, sudden injury.