The US regulator quietly delays action on a petition calling for the suspension of mRNA injections—despite evidence of regulatory failure, DNA contamination, and a surge in cancers among young people.
Maryanne thanks. Your warnings over months are so well researched and reported. This really is another thalidomide !!!
- if young person increased cancer is connected with the “purported” vaccine which is non trialed/assessed gene therapy.
Now for the real questions - which countries relied on Pfizer/FDA allowing millions of gene therapy doses and which countries didn’t
AND when are RWE (real world evidence) studies comparing vaccines (or gene therapy) used by national govts with trajectories of cancers by aged group.
I’m of course very angry (7 vax - 4 mRNA as that was all available)
It’s not only myself but children and grandchildren who were forced to have mRNA. Authorities stopped AZ, they stopped CSL replacing with gene therapy injections that needed repeating every 4 months to even be effective. Questionable if anything needed more frequently than 12 mths can ever be a vaccine?
This vaccine promotion and Pfizer’s antiviral drugs were used to dominate treatment / prevention whilst good simple antiviral nasal sprays were forcibly stopped in 2021 and Australians have to jump through whoops for respiratory virus protection and treatment importation
The WHO secret COLLUDING WITH global govts has impacted us All
• Relied on independent expert committees (like CHMP) and data submitted by Pfizer/BioNTech and Moderna, including raw trial data.
• In some cases, national authorities in EU countries conducted lot-release quality testing via official medicines control laboratories (OMCLs) under the EU Official Control Authority Batch Release (OCABR) system.
So:
• ✅ Yes, EMA and EU member states did independent regulatory and quality reviews.
• ❌ No, EMA did not re-run its own clinical trials or develop the vaccines themselves.
„Doctors for individual vaccine decisions“ („Ärzte für individuelle Impfentscheidung“, a small expert ngo on vaccines in Germany) just received an answer from the PEI (national institution for the safety of vaccines) claiming they had conducted their own tests on DNA contamination in Comirnaty (the BioNTech vaccine) on six samples supplied by the manufacturer. According to the PEI these tests were conducted by PEI’s own labs Nov/Dec 2023. No results were revealed due to third-party interests worthy of protection.
Regardless of what the FDA does on this one, at some stage in the next few years we will have a widespread realisation of the catastrophic impact of these terrible shots. The dam will eventually burst....
As a pfizer injured victim, I have seen many “exposures” during these last years but nothing comes of it. I held a bit of hope that the RFK Jr and his picks would expose the dangers and remove them from the market. Nope. Just as democratic senator Blumenthal noted “he’s seen the power of pharma up close.” Makary, Prasad, RFK JR, Bhattacharya are all on record denouncing the shots so what’s happened? Obviously something has intervened and my guess is Pharma, 1600 lobbyists, wealthy investors along with if exposed would cause such chaos, disruption and high anxiety and eventual lawsuits. The governments assured us it was safe and effective, and mandated the shots. This is a very tangled web and can’t see a way forward besides burying it.
“It will test courage” is something that has been lacking in public health “which was prepared to falsify and ignore data to survive.” There were medical professionals who had courage but were ground down by the medical industry. I hope RFK jr and others withstand the onslaught of pharma. There was a report just last week about Louisiana Republican Senator Cassidy waging a behind the scenes attempt to takeout RFK jr. While many people want an immediate stop to the COVID vaccine, there are many people who are either corrupt or totally not aware of the dangers. Public health, the medical industry, and major media have special culpability for the damages caused by lockdowns and the Covid vaccine.
They are unable to respond because they lack jurisdiction over biological countermeasures imposed under the PREP Act for the Covid-19 emergency. The clinical trials and hearings and EUAs are all to keep up the charade that these are medical products to be regulated and perhaps there were failures due to urgency expediency etc. As head of HHS, RFKjr could declare the emergency over and then FDA would have to do their jobs. See https://sashalatypova.substack.com/p/the-covid-dossier-updated-a-record
Maryanne thanks. Your warnings over months are so well researched and reported. This really is another thalidomide !!!
- if young person increased cancer is connected with the “purported” vaccine which is non trialed/assessed gene therapy.
Now for the real questions - which countries relied on Pfizer/FDA allowing millions of gene therapy doses and which countries didn’t
AND when are RWE (real world evidence) studies comparing vaccines (or gene therapy) used by national govts with trajectories of cancers by aged group.
I’m of course very angry (7 vax - 4 mRNA as that was all available)
It’s not only myself but children and grandchildren who were forced to have mRNA. Authorities stopped AZ, they stopped CSL replacing with gene therapy injections that needed repeating every 4 months to even be effective. Questionable if anything needed more frequently than 12 mths can ever be a vaccine?
This vaccine promotion and Pfizer’s antiviral drugs were used to dominate treatment / prevention whilst good simple antiviral nasal sprays were forcibly stopped in 2021 and Australians have to jump through whoops for respiratory virus protection and treatment importation
The WHO secret COLLUDING WITH global govts has impacted us All
I asked 🔴ChatGPT🔴 for info on where mRNA was distributed and what testing was done. Also where Sinovax was used.
I hope this is an accurate response as real global evaluation is surely required
Here’s a clear breakdown to answer your questions:
⸻
✅ Which countries used mRNA vaccines?
mRNA COVID-19 vaccines—Pfizer-BioNTech (Comirnaty) and Moderna (Spikevax)—were used primarily in:
• North America:
• USA, Canada (widespread use, early adopters)
• Europe:
• Most EU countries via EMA approval (e.g., Germany, France, Italy, etc.)
• UK (Pfizer, then also Moderna, via MHRA approval)
• Asia-Pacific:
• Australia, New Zealand, Japan, South Korea, Singapore
• Latin America:
• Chile, Uruguay, Argentina, Mexico (among others)
• Others:
• Israel, UAE, Saudi Arabia, etc.
⸻
🔬 Is Sinovac (CoronaVac) an mRNA vaccine?
No. Sinovac’s CoronaVac is NOT an mRNA vaccine. It is:
• A traditional inactivated virus vaccine
• It contains chemically inactivated SARS-CoV-2 virus particles to stimulate an immune response
• Used widely in China, Indonesia, Brazil, Chile, Turkey, and several African nations
⸻
🇪🇺 Did the European Medicines Agency (EMA) conduct independent testing of mRNA vaccines like Comirnaty?
Yes—but not in the way that implies in-house lab testing.
• The EMA did not conduct its own laboratory trials, but it required and reviewed all preclinical and clinical trial data from manufacturers.
• The European Medicines Agency:
• Assessed Phase 1–3 clinical trial data, manufacturing standards, and pharmacovigilance plans.
• Relied on independent expert committees (like CHMP) and data submitted by Pfizer/BioNTech and Moderna, including raw trial data.
• In some cases, national authorities in EU countries conducted lot-release quality testing via official medicines control laboratories (OMCLs) under the EU Official Control Authority Batch Release (OCABR) system.
So:
• ✅ Yes, EMA and EU member states did independent regulatory and quality reviews.
• ❌ No, EMA did not re-run its own clinical trials or develop the vaccines themselves.
„Doctors for individual vaccine decisions“ („Ärzte für individuelle Impfentscheidung“, a small expert ngo on vaccines in Germany) just received an answer from the PEI (national institution for the safety of vaccines) claiming they had conducted their own tests on DNA contamination in Comirnaty (the BioNTech vaccine) on six samples supplied by the manufacturer. According to the PEI these tests were conducted by PEI’s own labs Nov/Dec 2023. No results were revealed due to third-party interests worthy of protection.
@maryanne about three weeks ago I wrote you an email on a potential cooperation. Did you receive that? We’d be interested to join forces with you.
I don’t recall seeing an email—though I receive hundreds each week. Apologies if my reply is delayed; I’m currently travelling.
I can send it again if you want to. Safe travels!
It will be coming from markus.frieauff@individuelle-impfentscheidung.de
Regardless of what the FDA does on this one, at some stage in the next few years we will have a widespread realisation of the catastrophic impact of these terrible shots. The dam will eventually burst....
We can only hope for a reckoning.
FDA = Fools Delaying Action !
As a pfizer injured victim, I have seen many “exposures” during these last years but nothing comes of it. I held a bit of hope that the RFK Jr and his picks would expose the dangers and remove them from the market. Nope. Just as democratic senator Blumenthal noted “he’s seen the power of pharma up close.” Makary, Prasad, RFK JR, Bhattacharya are all on record denouncing the shots so what’s happened? Obviously something has intervened and my guess is Pharma, 1600 lobbyists, wealthy investors along with if exposed would cause such chaos, disruption and high anxiety and eventual lawsuits. The governments assured us it was safe and effective, and mandated the shots. This is a very tangled web and can’t see a way forward besides burying it.
Maybe it was an mRNA jab they took to protect themselves from the corrupto virus . . . . .
Such a long way to go. So many vested interests and lack of courage to take them on. The behemoth will not go down without a fight.
“It will test courage” is something that has been lacking in public health “which was prepared to falsify and ignore data to survive.” There were medical professionals who had courage but were ground down by the medical industry. I hope RFK jr and others withstand the onslaught of pharma. There was a report just last week about Louisiana Republican Senator Cassidy waging a behind the scenes attempt to takeout RFK jr. While many people want an immediate stop to the COVID vaccine, there are many people who are either corrupt or totally not aware of the dangers. Public health, the medical industry, and major media have special culpability for the damages caused by lockdowns and the Covid vaccine.
They are unable to respond because they lack jurisdiction over biological countermeasures imposed under the PREP Act for the Covid-19 emergency. The clinical trials and hearings and EUAs are all to keep up the charade that these are medical products to be regulated and perhaps there were failures due to urgency expediency etc. As head of HHS, RFKjr could declare the emergency over and then FDA would have to do their jobs. See https://sashalatypova.substack.com/p/the-covid-dossier-updated-a-record