BREAKING! Exposing Shocking Secrets: Why You Can Sue mRNA COVID Vaccine Manufacturers – 90 Lawyers Ready to Fight
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In a shocking turn of events, it has come to light that you now have the power to sue the manufacturers of mRNA COVID vaccines for damages, and the FDA is obligated to remove these vaccines from the market due to a grave issue – adulteration. Plasmid bioactive contaminant sequences, concealed from regulatory authorities, have tainted the integrity of these vaccines, making them a serious threat to public health. The FDA stands at a crossroads, and its decision could change the course of the COVID vaccine narrative forever.
As the world grapples with the ongoing COVID-19 pandemic, the race to develop and distribute vaccines has been a beacon of hope. mRNA vaccines, such as those developed by Pfizer, have played a pivotal role in this fight. However, recent revelations suggest that these vaccines may have a dark secret – adulteration.
Unveiling the Shocking Truth
The essence of this alarming revelation lies in the plasmid bioactive contaminant sequences that were deliberately withheld from regulatory authorities. This act, known as adulteration, raises critical questions about the safety and transparency of the mRNA COVID vaccines.
The implications are staggering: either the FDA was aware of the plasma contamination and failed to disclose it to the public and external committees, or they were unaware of it, making Pfizer liable. Compelling evidence in the form of Pfizer documents submitted to the FDA indicates a glaring absence of disclosure regarding SV40 contamination. This points to an adulterated vaccine that must be promptly removed from the market.
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The Urgent Need for Action
If the FDA fails to take swift action and withdraw these tainted vaccines from circulation, it should face criminal prosecution for jeopardizing public safety and disregarding the law. The stakes couldn’t be higher. As we delve deeper into this unprecedented controversy, let us explore the ramifications and what lies ahead for vaccine manufacturers, regulatory authorities, and the general public.
The Legal Crusade: 90 Lawyers Ready to Fight
For those seeking justice, there is hope. A list of 90 skilled lawyers stands ready to help you pursue legal action against the vaccine manufacturers. Your right to hold them accountable for damages is now more accessible than ever. Link to list of lawyers
The Shadow of SV40 Contamination
One of the most concerning aspects of this controversy is the potential presence of SV40 contamination. Simian Virus 40 (SV40) is a virus known to infect both monkeys and humans, and its presence in vaccines has sparked public outrage in the past. While there is no concrete evidence of SV40 contamination in the mRNA COVID vaccines, the absence of disclosure raises alarming questions.
The Gravity of Adulteration
Adulteration, as defined by the FDA, refers to the act of introducing impurities or contaminants into a product, compromising its safety and quality. In the case of mRNA COVID vaccines, the concealment of plasmid bioactive contaminant sequences fits this definition all too well.
FDA’s Dilemma: A Critical Decision
The FDA now finds itself at a crossroads. The agency must choose between two unsettling narratives. If they admit to prior knowledge of plasma contamination and its concealment, it raises questions about their role in safeguarding public health. Alternatively, if they claim ignorance, Pfizer becomes accountable for the lack of disclosure in its documents submitted to the FDA.
Public Safety vs. Profits: A Tense Standoff
At the heart of this controversy lies the balance between public safety and the interests of pharmaceutical giants. The public has a right to know if they are receiving vaccines that meet the highest safety standards, free from any contaminants. Failure to disclose such vital information undermines public trust and safety.
The Urgency of Transparency
Transparency is not a luxury; it is a necessity when it comes to public health matters. The revelations regarding the concealment of plasmid bioactive contaminant sequences demand immediate attention and disclosure. Public health agencies and pharmaceutical companies alike must prioritize transparency and accountability.
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The Call for Immediate Action
The consequences of inaction are dire. If the FDA fails to promptly remove adulterated vaccines from the market, it risks not only public health but also legal repercussions. The time for decisive action is now, and it is imperative that the FDA fulfills its obligation to safeguard the well-being of the public.
In a shocking turn of events, the revelation of plasmid bioactive contaminant sequences concealed from regulatory authorities has thrown the safety and transparency of mRNA COVID vaccines into question. The FDA faces a pivotal decision that could alter the course of the pandemic response and the future of vaccine development. Public trust is at stake, and accountability is paramount.
As you consider your options, remember that a list of 90 dedicated lawyers is ready to assist those seeking legal action against vaccine manufacturers. Your right to seek damages is a powerful tool in holding those responsible accountable.
In this era of unprecedented challenges, transparency and public safety must remain at the forefront. The decision made by the FDA in the coming days will reverberate through history, shaping the way we view vaccine development, regulatory oversight, and corporate responsibility. The clock is ticking, and the world watches with bated breath.
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2 Comments
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