Why Didn’t The Regulators See This?
Peak Prosperity
Chris Martenson
4.7 • 591 Ratings
🗓️ 1 March 2023
⏱️ 48 minutes
🧾️ Download transcript
Summary
The covid vaccine safety data collected by Pfizer and submitted to US, Australian and European regulators are packed with an unacceptable amount and variety of obvious vaccine-related concerns and probable harms. It screams “disaster!” These un-safety reports should have immediately led to the cessation of the shots or, at a minimum, kicked off deep inquiries into the signals to either rule them in or out.
Neither were done.
Transcript
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| 0:00.0 | Today we're going to be discussing three separate Pfizer safety documents on Cormonarity or the BNT 162 COVID vaccine. |
| 0:09.0 | I cannot believe the regulators in the United States and Europe and Australia individually and collectively missed what we're about to look at. |
| 0:17.0 | So, hey, thanks so much for being here. It's good to be back with you. It's always fun to be here doing what I do, which is scouting for information, spending a lot of time figuring out how to present it, and then being here with you talking about it and seeing what comes of it. Because it's time for us to move to common knowledge. We have to get there. It's way past time to get past this charade. We need to get on with some very important things in this world. |
| 0:40.0 | And it begins. |
| 0:41.3 | There can be no reconciliation without truth, they said, in ending apartheid in South Africa. |
| 0:46.9 | I agree with that. |
| 0:47.8 | I agree with the idea. |
| 0:48.8 | So let's get to the truth as much as we can. |
| 0:50.9 | And we'll start here by looking at the safety documents now. |
| 0:54.0 | We're looking at a |
| 0:55.0 | couple of them from the EU and Australia, but of course the FDA has these as well. Actually, one |
| 1:01.7 | from one from the US as well. So here are the three that we're going to be reviewing. This is the |
| 1:06.4 | first one. I reviewed this one many months ago, and this was the first 2.3 months, as it were, |
| 1:13.5 | about two months of safety data that Pfizer had collected in what's called post-marketing |
| 1:18.6 | surveillance, so that's cumulative analysis of post-authorization, adverse event reports, |
| 1:24.1 | and this was from through the 28th of February 2021. And of course, they started |
| 1:28.9 | with the vaccinations on the 19th of December 2020. Here's another report. This is the PSUR. This is |
| 1:36.4 | out of the EMA's grasp in Europe. So the periodic safety update report, and this is from |
| 1:42.9 | December 19th, 2020 through the 18th of June 2021, so six months there. |
| 1:50.1 | And as well, just released through FOIA and we just got our hands on it from Australia is this one here, which is the cumulative number of case reports. |
| 1:59.2 | This is a total of 16 months of data and as of April 16th, |
| 2:05.2 | 2022. So when we compare all three of these, we should be able to get a pretty decent picture and we |
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