Dr. Robert Chandler - In the Adverse Event Reports, 77% were women. | Clip

Pfizer Papers contributing author Dr. Robert Chandler:

"Vinny Prasad & Marty Makary...are unable to independently evaluate information...you're telling us this is just for old people...We're easy to bump off anyway, so you save this toxic poison for us...?"

This clip of Chandler, an esteemed (retired) orthopedic surgeon who has significantly advanced orthopedic surgery through clinical trials and medical management, is taken from a discussion with Liz Gunn and VAERSAware creator Albert Benavides posted to Rumble on May 30, 2025.

---------------Partial transcription of clip---------------

"The two that I found just totally disappointing were Vinny Prasad and Marty Makary. And I've concluded these two are unable to independently evaluate information. And, because the amount of stuff that the researchers around the world have produced, whether you look at peer review or this less formal stuff stuff, it's massive. It's absolutely massive.

"And to have a split-the-baby-type approach, which, I don't know if you saw their article in New England Journal of Medicine, you just go, okay, so now you're telling us this is just for old people like me that have a bunch of medical problems. We're easy to bump off anyway, and so you save this toxic poison for us old people?

"Well, I'm happy to hear the kids are spared, but, I'm not sure they pull the pregnant women out of there, which is. They have not. They have not. Which is totally unforgivable. Totally unforgivable. Because we identified early, when we got the Rosetta, stone for the clinical work is document 5.3.6, which summaries the pharmacovigilance in the first 10 weeks in the US and 12 weeks in the UK. It was just, my eyes fell out of my head because I looked at the female/male, discrepancy in the adverse event reports, and it was like 77% were women.

"Then as we got more and more information, 16% of those adverse events affected the reproductive system, compared to less than 1% of males. What accounts for this? And when some of, Albert's favorites, Manish. When they looked at the data in Sweden. In, Sweden... But they found 80% of the adverse events in the early lots were, in women. And, then they cooled off. They changed. This is something that should have ended it immediately.

"They changed the process from the clinical trials to the release in December of 2020. It was a different formulation, which means it's a different drug, which means you've got to go back all the way to the animal testing and, and go through the phase three trials. No, they didn't do that. They just produced it in bulk and started injecting it in billions of people. It's totally untested. And that's when the process two came to light and we realised that the, vaccine was contaminated with bacterial DNA that can incorporate into the human genome, apparently. So there's a lot of detail here, and that alone should have killed it."

Sense Receptor on the clip - https://x.com/SenseReceptor/status/1928990671173452262

Full interview - https://rumble.com/v6u3y9h-vaers-myocarditis-data-cover-up-with-dr.-robert-chandler-and-albert-benavid.html?e9s=src_v1_ucp