Because the COVID gene-based Spike injections (incorrectly referred to as “vaccines”) were developed, tested and released in only 10 months, many of the usual safety tests were either not conducted or were compromised. Drug regulatory agencies around the world, including the US FDA, our Therapeutic Goods Administration (TGA) and the European Medicines Agency (EMA), rightly requested ongoing and timely adverse event reporting to roughly assess the safety of these injections as a condition of the conditional approval of the injections.
These adverse event reporting systems rely upon the goodwill and cooperation of health professionals to take the time to report adverse events which occur post-injection although patients and family members can also report. However, it is widely accepted that only a small fraction of adverse events are ever reported. In the case of the COVID gene-based Spike injections probably only about 1-2% of adverse events are ever reported because health professionals fear any such reporting may be interpreted as undermining the prevailing government narrative that the injections are “safe”.
The Pfizer Periodic Safety Update Report (PSUR) # 3 has just been made public. You might well ask……where are PSUR reports #1 and #2? Anyway……
PSUR #3 (up to August 2022) shows the following (the current numbers will be far higher):
1.6 million adverse events covering nearly every organ system.
•73,542 vascular disorders •696,508 nervous system disorders
•61,518 eye disorders
•47,000 ear disorders
•225,000 skin and tissue disorders
•178,000 reproductive disorders
•190,000 respiratory disorders
•77,000 psychiatric disorders
•127,000 cardiac disorders
•100,000 blood disorders
•3,711 tumors
CLICK HERE for the full 400 page PSUR #3.
CLICK HERE for a brief overview of the report release by Daniel Horowitz on 14 June 2023.
The adverse event rate in women is 3 times that of men!
60% of adverse events reported were either classified as “outcome unknown” or “not recovered” thus indicating sustained injuries.
The highest number of cases occurred in the 31-50 year age group and 92% did not have any comorbidities thus suggesting the injections were the cause of the reported adverse effects.
It is now wonder that it was reported that soon after the COVID gene-based Spike injections were rolled out, Pfizer needed to hire more than 2000 employees to deal with the flood of adverse event reports. Nothing like this has ever been seen previously.
Australia seems to have been hit particularly hard in relation to adverse effects following the injections. Watch Dr. John Campbell’s latest review of cardiac deaths in Australia. CLICK HERE to view.
I encourage all to take responsibility for your own health and to learn what this means for each one of us . It’s not as “ convenient “ as relying on your doctor but it’s a breathtakingly exciting journey into informed consent.
Thanks Phillip.
It may be a higher rate of reporting for woman, but as we all know men are hesitant to report most stuff that is wrong with them to Doctors or the TGA( that’s of course if they know it exists) and wait to see if they can fix it themselves.