Components of mRNA Technology “Could Lead to Significant Adverse Events in One or More of Our Clinical Trials,” says Moderna
Summary:
- mRNA vaccines undergoing Covid-19 clinical trials, including the Moderna vaccine, rely on a nanoparticle-based “carrier system” containing a synthetic chemical called polyethylene glycol (PEG).
- The use of PEG in drugs and vaccines is increasingly controversial due to the well-documented incidence of adverse PEG-related immune reactions, including life-threatening anaphylaxis.
- Roughly seven in ten Americans may already be sensitized to PEG, which may result in reduced efficacy of the vaccine and an increase in adverse side effects.
- If a PEG-containing mRNA vaccine for Covid-19 gains FDA approval, the uptick in exposure to PEG will be unprecedented—and potentially disastrous.
- Moderna documents and publications indicate that the company is well aware of safety risks associated with PEG and other aspects of its mRNA technology but is more concerned with its bottom line.
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Questioning the Use of PEGylation for Drug Delivery
Abstract
Polyethylene glycol (PEG) is widely utilized in drug delivery and nanotechnology due to its reported “stealth” properties and biocompatibility. It is generally thought that PEGylation allows particulate delivery systems and biomaterials to evade the immune system and thereby prolong circulation lifetimes. However, numerous studies over the past decade have demonstrated that PEGylation causes significant reductions in drug delivery, including enhanced serum protein binding, reduced uptake by target cells, and the elicitation of an immune response that facilitates clearance in vivo. This report reviews some of the extensive literature documenting the detrimental effects of PEGylation, and thereby questions the wisdom behind employing this strategy in drug development.
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VACCINE DEATH WAVE: UK government posts bid for AI system to process the expected flood of COVID-19 vaccine injuries and side effects described as a “direct threat to patient life”
Monday, November 16, 2020 by: Mike Adams
(Natural News) While the lying, treasonous mainstream media is telling us all that covid-19 vaccines are perfectly safe and “95% effective” — and this lie is being repeated by PJ Media, Breitbart and other so-called “conservative” news publishers — the UK government has posted a bid and an award contract notice, seeking an Artificial Intelligence (AI) system that can process the expected flood of covid-19 vaccine injuries and side effects.
Titled simply, “Supplies – 506291-2020” and found at this link on Tenders Electronic Daily, this contract award notice we originally posted on October 19th, 2020 and is summed up as follows:
The MHRA urgently seeks an Artificial Intelligence (AI) software tool to process the expected high volume of Covid-19 vaccine Adverse Drug Reaction (ADRs) and ensure that no details from the ADRs’ reaction text are missed.
The request for the AI system to process covid-19 vaccine reactions comes from the UK’s Medicines & Healthcare Products Regulatory Agency, the MHRA.
Further in the document, the MHRA describes an “extreme urgency under Regulation 32(2)(c) related to the release of a Covid-19 vaccine” and says that the expected flood of covid-19 vaccine adverse reactions will overwhelm its current “legacy systems.”
“If the MHRA does not implement the AI tool,” the MHRA explains, “it will be unable to process these ADRs effectively. This will hinder its ability to rapidly identify any potential safety issues with the Covid-19 vaccine and represents a direct threat to patient life and public health.”
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The shocking reason why Pfizer’s coronavirus vaccine requires storage at -70C … because it contains experimental nanotech components that have NEVER been used in vaccines before
Wednesday, November 18, 2020 by: Mike Adams
Tags: adverse reactions, badhealth, badmedicine, coronavirus, genocide, Moderna, mRNA, nanotechnology, Pfizer, side effects, vaccine wars, vaccines
(Natural News) You’re seeing the reports all over the news: Pfizer’s new coronavirus vaccine requires storage at -70C (-94F), which is much colder than the North Pole. If it’s not stored at this temperature, its ingredients begin to break down and it fails to work. Currently Pfizer is claiming, without evidence, that its vaccine is “90% effective.” But this claim is little more than corporate propaganda designed to drive up stock prices through false projections.
But why do these vaccines need to be kept at -70C in the first place?
The answer, it turns out, is because they contain potentially hazardous ingredients that have never been used in vaccines before.
As Children’s Health Defense explained in an August 6th article, “mRNA vaccines undergoing Covid-19 clinical trials, including the Moderna vaccine, rely on a nanoparticle-based “carrier system” containing a synthetic chemical called polyethylene glycol (PEG).”
CHD goes on to explain:
The use of PEG in drugs and vaccines is increasingly controversial due to the well-documented incidence of adverse PEG-related immune reactions, including life-threatening anaphylaxis.
Roughly seven in ten Americans may already be sensitized to PEG, which may result in reduced efficacy of the vaccine and an increase in adverse side effects.
If a PEG-containing mRNA vaccine for Covid-19 gains FDA approval, the uptick in exposure to PEG will be unprecedented—and potentially disastrous.
Moderna documents and publications indicate that the company is well aware of safety risks associated with PEG and other aspects of its mRNA technology but is more concerned with its bottom line.
