Pfizer COVID Vaccine Safety Report Identified Nearly 1.6 Million Adverse Events Early On

Original article here.

By June of  2022, Pfizer had identified over 10,000 categories of nearly 1.6 million adverse events, a recently-released safety update report shows. Pfizer’s pharmacovigilance documents were requested and released by the European Medicines Agency, the EU’s drug regulator, Conservative Review’s Daniel Horowitz reported on Wednesday.

The 396-page confidential Pfizer report, dated August 18, 2022, reveals that Pfizer was well aware its product was causing an unacceptable level of serious and debilitating injuries early on.

In the reporting period of December 19, 2021 through June 18, 2022, the company observed 1,597,673 adverse events in 508,351 case reports—one-third of them classified as serious.

The report also shows that women reported adverse events at three times the rate of men, although many of their complaints were not considered serious.

Signals that were addressed and inexplicably “determined not to be risks” include heavy menstrual bleeding, loss of taste and smell, Appendicitis, Hemolytic Anemia, uveitis, flareups of autoimmune disease and inflammatory disorders, and vasculitis. Signals that were determined to be important identified risks included Anaphylaxis, Myocarditis and Pericarditis. “Hearing loss” was catalogued as an  “ongoing signal.”

The report also acknowledged that Vaccine-Associated Enhanced Disease (VAED) and Vaccine-Associated Enhanced Respiratory Disease (VAERD) were important potential risks of taking the shot. The report indicated that it was “missing information on the potential risks for pregnant or breastfeeding mothers, immunocompromised individuals and use in frail patients with comorbidities. Regardless, the mRNA injections were strongly recommended for everyone, and for most working aged individuals, it was mandated.

The Pfizer data shows that more than 60 percent of cases were classified as either “outcome unknown” or “not recovered,” indicating that a concerning number of the injuries were long term. Only 35 percent were listed as recovered or recovering.

The highest number of cases thus occurred in the 31-50 year-old group,  92 percent of whom did not have any comorbidities prior to the jab.

Conservative Review also highlighted a recently released Pfizer summary documenting “serious and non-serious adverse reactions from post-marketing data sources” dated “as of June 18, 2022.”

The data show:

•  Pfizer was aware of 73,542 cases of 264 categories of vascular disorders from the shots. Many of them are rare conditions.
•  There were hundreds of categories of nervous system disorders, totaling 696,508 cases.
•  There were 61,518 AEs from well over 100 categories of eye disorders, which is unusual for a vaccine injury.
•  Likewise, there were over 47,000 ear disorders, including almost 16,000 cases of tinnitus, which even Mayo Clinic researchers observed as a common but often devastating side effect early on.
•  There were roughly 225,000 cases of skin and tissue disorders.
•  here were roughly 190,000 cases of respiratory disorders.
•  Disturbingly, there were over 178,000 cases of reproductive or breast disorders, including disorders you wouldn’t expect, such as 506 cases of erectile dysfunction in men.
• Very disturbingly, there were over 77,000 psychiatric disorders observed following the shots, lending credence to Dr. Peter McCullough’s research observing case studies showing psychosis correlating with vaccination.
•  3,711 cases of tumors – benign and malignant
• Of course, there were almost 127,000 cardiac disorders, running the gamut of about 270 categories of heart damage, including many rare disorders, in addition to myocarditis.
• There were over 100,000 blood and lymphatic disorders, for both of which there’s a wealth of literature linking them to the spike protein.

“When reading what Pfizer knew early on juxtaposed to independent studies, it’s clear that nobody could have mistaken most of these AEs for mere incidental ailments,” Horowitz wrote.