COVID-19
Health Canada received over a million reports of COVID vaccine adverse events: records
From LifeSiteNews
As reported first by True North, according to Access to Information correspondence, from December 2020 to December 2022 Health Canada got over a million serious adverse event reports regarding the COVID vaccines.
Newly uncovered records have revealed that during the so-called pandemic thousands of serious adverse event reports related to the mRNA COVID jabs were reported to Health Canada each day, at the same time public health officials and the media claimed the experimental vaccines were safe.
As reported first by True North, according to Access to Information (ATIP) correspondence, from December 2020 to December 2022 Health Canada got over a million serious adverse events (SAE) reports regarding the COVID vaccines from Pfizer, AstraZeneca, Moderna and Janssen. Broken down, some 600,000 of the reports related to the Pfizer jab, 220,000 to AstraZeneca, 160,000 to Moderna and 22,000 to Janssen. Of note is that the Pfizer jab was the most widely distributed in Canada.
As per regulations, pharmaceutical companies must report SAE that happen anywhere in the world to Canada’s public health minister within “15 days after receiving or becoming aware of the information.”
The access to information coordinator noted that a “broader interpretation (of your request) could encompass millions of records,” adding that as they had a “processing capacity of about 500 pages per month,” handling such a large volume would “require a significant amount of time to complete.”
Broken down, if one serious adverse event report totals just a page each, at the given processing speed, it would take 167 years before all the SAEs would be processed.
The first COVID jab to be approved for use in Canada was Pfizer’s BioNTech mRNA injection, which became available on December 9, 2020. Moderna’s mRNA jab soon followed a couple of weeks later. Of important note is the launch of the jabs came after the government of Prime Minister Justin Trudeau gave vaccine makers a shield from liability regarding jab-related injuries.
Health minister would have seen SAE submissions
By June of 2021, the SAE submissions just for the Pfizer shot totaled over 100,000 reports worldwide, with some 820 in Canada alone. Canada’s then-Minister of Health Patty Hadju would have had information at this time from the various drug jab makers showing how many SAEs there were both domestically and worldwide.
It is estimated that overall Health Canada was getting about 10,000 SAE reports from worldwide sources every week.
All levels of Canadian government heavily promoted the COVID shots, regularly touting them as both “safe and effective.”
However, LifeSiteNews has published an extensive amount of research on the dangers of the experimental COVID mRNA jabs, which include heart damage and blood clots.
The mRNA shots have also been linked to a multitude of negative and often severe side effects in children and all have connections to cell lines derived from aborted babies.
Brownstone Institute
Big Pharma Continues to Hide the Truth
From the Brownstone Institute
By
On Thursday, Joe Rogan and Marvel megastar Josh Brolin traded stories about the preponderance of Covid vaccine injuries among their friends. Brolin even described contracting “a mild case of Bell’s palsy” earlier this year, which Rogan attributed to the vaccine, noting he knew several people who suffered facial paralysis following Covid vaccination.
There is no perfect medicine. The benefits and harms of any treatment must be carefully considered in order to prescribe the safest, most effective course of action for a patient. While the FDA and CDC continue to extol the benefits of the Covid vaccines, they have ignored a growing body of evidence that these products can also be harmful. The code of medical ethics demands a transparent and balanced accounting of their impact on the American people. Only then can we set the best course for healthcare policy and future pandemics.
An honest accounting begins with clinical trials, supposedly “the most rigorous in history.” Pfizer’s own legal arguments suggest otherwise. Responding to a whistleblower lawsuit alleging major deviations from protocol, Pfizer’s lawyers noted that the company’s “Other Transactions Authority” agreement (OTA) with the Pentagon didn’t require clinical trials to comply with FDA regulations because the vaccine was a military prototype for “medical countermeasures.” This agreement allowed Pfizer to “grade its own homework,” so to speak — a point emphasized by DOJ lawyers in a separate filing in Pfizer’s support.
The FDA intended to keep Pfizer’s data hidden for 75 years, but attorney Aaron Siri’s FOIA lawsuit forced the agency to release them. Naomi Wolf’s DailyClout led 3,250 volunteer experts in analyzing more than 450,000 pages of internal Pfizer documents and uncovered massive harms ignored by the FDA, detailed in The Pfizer Papers: Pfizer’s Crimes Against Humanity.
This effort revealed 1,233 deaths in the first three months of the vaccine rollout, and a litany of injuries: “industrial-scale blood diseases: blood clots, lung clots, leg clots; thrombotic thrombocytopenia, a clotting disease of the blood vessels; vasculitis, dementias, tremors, Parkinson’s, Alzheimer’s, epilepsies.”
These harms are echoed by data from V-safe, a smartphone-based tool created by the CDC. Among 10.1 million registered V-safe users, 7.7 percent reported side effects so serious they were compelled to seek medical care, many more than once.
The main culprit is the Covid spike protein encoded in the vaccine’s mRNA technology. This protein is an antigen, or foreign immunogenic substance, located on the outer coat of the SARS-CoV-2 virus, that triggers an immune response. The mRNA in the shots instructs the body’s cells to produce identical spike proteins, inducing the immune system to create antibodies that bind to them, theoretically protecting vaccinated individuals against the virus. Unfortunately, this plan has a fatal flaw: The spike itself is toxic and potentially deadly.
Hundreds of peer-reviewed articles have demonstrated the spike’s potential for harm independent of the rest of the virus. Potential complications include myocarditis, blood clots, neurological injuries, and immune dysfunction. Pfizer’s own pre-market biodistribution studies show that vaccine components leave the injection site in the arm and penetrate every major organ system within hours, where mRNA can linger for weeks, forcing cells to churn out more and more of the toxic spike protein, which can persist for months. There is no way to predict how much spike protein the mRNA injections will produce in any individual, and there is no “off switch.”
According to CDC figures analyzed in Toxic Shot: Facing the Dangers of the COVID “Vaccines,” from 2021-2023 the US suffered 600,000 excess deaths not associated with Covid. Furthermore, Bureau of Labor Statistics data reveal that two million Americans became newly disabled, with unusual excesses in historically low-risk groups.
These trends coincided with mass Covid vaccination, including an unaccountable 59 percent surge in deaths among Americans ages 15-44 in the third quarter of 2021 compared to 2019. Crucially Covid contributed only part of this excess mortality: in that quarter the US suffered around 201,000 excess deaths, with Covid officially accounting for 123,000, leaving 78,000 excess deaths — 39 percent of the total — still unexplained.
Similar figures from abroad underscore a tragic loss of life among healthy people at minimal serious risk from the virus.
It could get worse. No carcinogenicity studies were performed on the injections prior to their launch, thus long-term cancer risks are essentially unknown. The spike protein also appears prone to prion-like misfolding, raising the specter of potential neurodegenerative disorders.
Medical ethics demand a balanced approach to every intervention, weighing potential benefits against potential harms. However, in the case of the Covid vaccines, federal agencies have chosen only to proclaim benefits. By surfacing data that bear upon both the positive and negative impacts of the Covid vaccines, and evaluating the pandemic performance of CDC, FDA, and other health agencies, the new administration can restore confidence and integrity in medicine and public health.
Republished from The Federalist
COVID-19
Mel Gibson tells Joe Rogan about alternative cancer treatments, dangers of Remdesivir
From LifeSiteNews
By Stephen Kokx
In the wide-ranging interview, Mel Gibson told Joe Rogan about his experience with Remdesivir, the pharmaceutical industry and alternative treatments for cancer.
Mel Gibson discussed a wide range of issues with podcaster Joe Rogan this week, almost all of them eliciting strong reactions on social media, especially his comments on cancer and the medical establishment.
Gibson contracted COVID-19 in April 2020. During a week-long hospital stay, he was administered the dangerous drug Remdesivir, which, despite having been known to have a mortality rate of over 50 percent in trials, was approved by Dr. Anthony Fauci for use in hospitals during the pandemic.
Gibson told Rogan that the experimental treatment nearly ended his life.
“[Remdesivir] kills you. I found that afterward. And that’s why I wonder about Fauci,” Gibson said.
Hospitals were incentivized to use Remdesivir, which has been shown to cause kidney failure, after the U.S. government approved a 20 percent reimbursement bonus for its use. Medical facilities also obtained money from the government for classifying deaths as being due to COVID-19. Critics allege that those policies enticed medical professionals to use the risky treatment in order to kill patients as a way to unethically boost profits.
Gibson told Rogan that he acquired COVID from his gardener, who he had known for twenty years, but that he did not survive his illness.
“We both went to the same hospital, and he died, and I didn’t … I think we both got Remdesivir, which is not good,” he explained.
“I don’t know why Fauci’s still walking around… or at least free,” he further remarked.
Gibson and Rogan also talked about cancer and Big Pharma. Gibson revealed that he knows people who have been healed from the illness due to alternative treatments.
“I have three friends. All three of them had stage 4 cancer. All three of whom don’t have cancer right now at all. And they had some serious stuff going on,” Gibson said.
“And what did they take?” Rogan asked.
“They took …what you’ve heard they’ve taken,” he replied.
“Ivermectin, Fenbendazole,” Rogan said. “I’m hearing that a lot.”
“They drank hydrochloride something or other … people drinking methylene blue,” Gibson said.
“There’s a lot of stuff that does work, which is very strange,” Rogan remarked. “Because, again, it’s profit, when you hear about things that are demonized and they turn out to be effective, you always wonder: ‘what is going on here?’ How is [sic] our medical institutions, how have they failed us so that things that do cure you are not promoted because they’re not profitable? They can’t control it. They don’t have a patent on it. Whether it’s Vitamin D, K2, Magnesium, Zinc. I do all that stuff.”
On Friday morning, an X-approved post titled “Mel Gibson’s Cancer Cure Claim Sparks Medical Debate” was published on the trending section. Some users piggybacked on Gibson’s remarks by stating that they too have used or know people who are using treatments similar to the ones Gibson’s friends did and that “cancer research” is a racket.
Others were unconvinced and re-iterated the media narrative that ivermectin is a simply a “dewormer.”
Elsewhere in their conversation, Gibson defended the authenticity of the Shroud of Turin and the historical reality of the resurrection of Christ, a topic Rogan has seemingly taken a heightened interest in recently given that he discussed the matter in depth on his show with a Protestant guest less than two weeks ago.
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