"Garbage Soup": Alexandra Latypova on Regulatory and Manufacturing Fraud in C-19 Injections
Two Soviet expats talk about medical fraud and living under the mob.
This story is about my conversation with Alexanda Latypova, a Soviet expat and pharmaceutical industry expert.
Alexandra grew up in Soviet Ukraine and immigrated to America in the late 1990s. She got her MBA from Dartmouth College and the spent about twenty five years in pharmaceutical industry and biotech (including in the areas of drug safety and clinical trials).
Alexandra has been a successful entrepreneur. She has founded a number of startups, sold them several years ago, and retired, hoping to focus on pleasant things like painting (she is a great artist), traveling, etc.
But life planned differently, and when 2020 came, she smelled the rat early on on due to many “abnormalities” related to “COVID response,” including the very strange coordinated campaign to prevent effective treatment of COVID.
Compelled to understand what was going on, Alexandra rolled up her sleeves and got to work. For starters, she started looking at VAERS, and she discovered unreasonable discrepancies between different lots, where some lots had just a few reported severe adverse events, and some had thousands (she later learned from FOIA’ed documents that lot sizes were in a relatively similar range).
In the interview, Alexandra also talks about a very uneven distribution of “lot mortality” in the U.S. where the coasts did relatively okay, while some midwestern states had very poorly, with very high numbers of reported deaths per a hundred thousand doses. The worst state is South Dakota (30 reported deaths per 100,000 shipped doses). The areas that did even worse, according to Sasha, were some of the U.S. territories with high percentage of indigenous population (this slide from the presentation was made before that latter data became available.)
Another point that Alexandra highlights is the total, compete, and Soviet-like lack of any compliance to any expected standards of, well, anything, in all phases of development and production of this product. Not only did they skip important phases of clinical trials (which was known, and explained away by “warp speed,” etc.), there is no described procedure testing of vials, have also been blatant fabrications and distorion of facts, which, accoring to Alexandra, would have been very hard to pull off without conscious and deliberate “protection” of the manufacturers by the regulatory organs.
Furthermore, as Sasha points out, VAERS is the only publicly available database, designed as a signal (and let’s not forget the old Harvard Health study that showed that VAERS was severaly underreported—NOT overreported—capturing around 1% if actual adverse events). But in addition to VAERS, the health official currently have several other, relatively rigorously maintained, internal databases tracking adverse effects, and they have had access to all the data on carnage in real time. And they watched it. And they saw carnage. And they lied about it to our faces and to the faces of the vaccines injured and their loved ones.
An example of fraud: A Moderna maternal toxicity study (which seeminly was the only study they did, on rats, and only on female rats only) Moderna found a signal where a statistically significant portion of offspring of vaccinated female rats had developed skeletal malformations. And what did Moderna do after finding it and documenting it in their internal papers, FOIA’ed by Judicial Watch? They said that no issues had been found. Etc. etc. Things like that, from horizon to horizon!
She goes over everything in detail in the interview, and she also kindly allowed me to share the PDF of her presentation in case you like to read vs. watch.
But before I go into more detail, I would like to point out that besides being a super sharp, courageous, outspoken human being, she is a trained and very talented artist. Below are a couple of Sasha’s paintings. I am in awe of her talent!