Big Pharma Forced To Yank COVID Vaxx Study Due To Lack Of Participants​

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Two of the major pharmaceutical companies connected with the controversial COVID vaccineswere forced to abandon a new research study after failing to garner enough participants.

Pfizer and German vax maker BioNTech had sought to research an updated version of the vaccine in adults ages 50 to 64, but were unable to generate the data needed due to the low enrollment in the trials, Reuters reported.

The study was needed in order to meet new guidelines imposed by the Food and Drug Administration that require the pharmaceutical companies to provide data on the efficacy of the vaccine in comparison with a placebo.

However, it marks a peculiar coda to the pandemic era, when mass formation psychosis swept the globe forcing individuals to forgo their civil liberties en masse and to inject the experimental, gene-altering serum into their DNA under extreme social duress.

Since then, vaccine injuries including strokes, myocarditis, turbo cancers and miscarriages have all been linked, either clinically or anecdotally, to the drugs, which were fast-tracked by the FDA under the previous Trump and Biden administrations with backing from dubious medical authorities like COVID czar Anthony Fauci.

In addition to the potential harm the caused, others have noted that the vaccines had little benefit since they did not prevent transmission of the COVID virus.

The pandemic ultimately dissipated as the result of natural immunity and evolution, with weaker variants rendering the vaccines unnecessary and redundant.

The stricter FDA guidelines under current Health and Human Services Sec. Robert F. Kennedy Jr.stand in stark contrast with the early days of the Biden presidency, when Kennedy’s far-left counterpart, Xavier Becerra, oversaw unconstitutional mandates pressuring government workers and various private industries to submit to the demands of Big Pharma.

Jeffrey Tucker, president of the Brownstone Institute — a nonprofit that sprung up in opposition to vaccine mandates and other COVID-era hysteria — said the recent fizzling of Pfizer offered a long-awaited dose of poetic justice.

“Essentially, the market itself is taking the Covid shots off the market,” Tucker wrote in an X post.

“It amounts to a humiliating repudiation of one of history’s largest and most destructive inoculation attempts. A fitting end to a hideous story.”
 

Big Pharma Forced To Yank COVID Vaxx Study Due To Lack Of Participants​

source/archive

View attachment 55404

Two of the major pharmaceutical companies connected with the controversial COVID vaccineswere forced to abandon a new research study after failing to garner enough participants.

Pfizer and German vax maker BioNTech had sought to research an updated version of the vaccine in adults ages 50 to 64, but were unable to generate the data needed due to the low enrollment in the trials, Reuters reported.

The study was needed in order to meet new guidelines imposed by the Food and Drug Administration that require the pharmaceutical companies to provide data on the efficacy of the vaccine in comparison with a placebo.

However, it marks a peculiar coda to the pandemic era, when mass formation psychosis swept the globe forcing individuals to forgo their civil liberties en masse and to inject the experimental, gene-altering serum into their DNA under extreme social duress.

Since then, vaccine injuries including strokes, myocarditis, turbo cancers and miscarriages have all been linked, either clinically or anecdotally, to the drugs, which were fast-tracked by the FDA under the previous Trump and Biden administrations with backing from dubious medical authorities like COVID czar Anthony Fauci.

In addition to the potential harm the caused, others have noted that the vaccines had little benefit since they did not prevent transmission of the COVID virus.

The pandemic ultimately dissipated as the result of natural immunity and evolution, with weaker variants rendering the vaccines unnecessary and redundant.

The stricter FDA guidelines under current Health and Human Services Sec. Robert F. Kennedy Jr.stand in stark contrast with the early days of the Biden presidency, when Kennedy’s far-left counterpart, Xavier Becerra, oversaw unconstitutional mandates pressuring government workers and various private industries to submit to the demands of Big Pharma.

Jeffrey Tucker, president of the Brownstone Institute — a nonprofit that sprung up in opposition to vaccine mandates and other COVID-era hysteria — said the recent fizzling of Pfizer offered a long-awaited dose of poetic justice.

“Essentially, the market itself is taking the Covid shots off the market,” Tucker wrote in an X post.

“It amounts to a humiliating repudiation of one of history’s largest and most destructive inoculation attempts. A fitting end to a hideous story.”
>zerohedge
 

Biden FDA Knew About COVID Vaccine Stroke Risk And Kept Americans In The Dark​

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Senate investigators spent months reviewing roughly 2,000 pages of federal records. What they found is damning. FDA and CDC officials under the Biden administration identified a significant stroke risk tied to Pfizer's COVID-19 bivalent booster in seniors - and never breathed a word to the public.

Sen. Ron Johnson (R-WI), chairman of the Senate's Permanent Subcommittee on Investigations, sent a formal letter to HHS Secretary Robert F. Kennedy Jr. laying out the evidence. He wasn't speculating. He was citing the government's own files.

"HHS records show that as early as October 2022, federal health officials identified a connection between the Pfizer-BioNTech COVID-19 bivalent booster and ischemic stroke for individuals over the age of 65," Johnson wrote.

An ischemic stroke means a blockage of blood to the brain. Between November 2022 and March 2023, seven separate analyses of incoming data flagged the same stroke signal — specifically in adults over 65.

CDC data cited by Johnson shows 226 stroke cases reported between August 2022 and February 2023, with additional cases surfacing throughout 2023 and 2024.

Despite the risk, the Biden administration issued no formal warnings. No Health Alert Network message. No changes to booster recommendations for seniors. Nothing.

Instead, in February 2023, HHS quietly hired a private contractor, Lukos LLC, to conduct a deeper internal investigation, dubbed "The Stroke Project." Publicly, officials kept insisting the vaccines were safe.

"From the initial detection of the safety signal in late 2022 … health officials continued to say the vaccine was safe while simultaneously searching for evidence to support that assertion,” Johnson said.

It gets worse. Federal officials drafted a communications plan about the stroke risk that included a "Tough Questions and Answers" section prepared for President-ish Biden and his White House team. During final edits, the description of the stroke signal was quietly changed from "moderately elevated" to "slightly elevated." Who made that change? Nobody knows. The language softened, the edit went unattributed, and the public remained in the dark.

The pattern is consistent. Senate investigators previously established that Biden officials also downplayed the risk of vaccine-induced myocarditis and kept that from the public. This wasn't a one-time failure. It was a system.

The fallout from that kind of institutional betrayal is hard to overstate. According to the Kaiser Family Foundation, fewer than half of all Americans now trust the CDC and FDA to operate free from political or special-interest influence.
 

Biden FDA Knew About COVID Vaccine Stroke Risk And Kept Americans In The Dark​

sauce/archive

View attachment 55986

Senate investigators spent months reviewing roughly 2,000 pages of federal records. What they found is damning. FDA and CDC officials under the Biden administration identified a significant stroke risk tied to Pfizer's COVID-19 bivalent booster in seniors - and never breathed a word to the public.

Sen. Ron Johnson (R-WI), chairman of the Senate's Permanent Subcommittee on Investigations, sent a formal letter to HHS Secretary Robert F. Kennedy Jr. laying out the evidence. He wasn't speculating. He was citing the government's own files.

"HHS records show that as early as October 2022, federal health officials identified a connection between the Pfizer-BioNTech COVID-19 bivalent booster and ischemic stroke for individuals over the age of 65," Johnson wrote.

An ischemic stroke means a blockage of blood to the brain. Between November 2022 and March 2023, seven separate analyses of incoming data flagged the same stroke signal — specifically in adults over 65.

CDC data cited by Johnson shows 226 stroke cases reported between August 2022 and February 2023, with additional cases surfacing throughout 2023 and 2024.

Despite the risk, the Biden administration issued no formal warnings. No Health Alert Network message. No changes to booster recommendations for seniors. Nothing.

Instead, in February 2023, HHS quietly hired a private contractor, Lukos LLC, to conduct a deeper internal investigation, dubbed "The Stroke Project." Publicly, officials kept insisting the vaccines were safe.

"From the initial detection of the safety signal in late 2022 … health officials continued to say the vaccine was safe while simultaneously searching for evidence to support that assertion,” Johnson said.

It gets worse. Federal officials drafted a communications plan about the stroke risk that included a "Tough Questions and Answers" section prepared for President-ish Biden and his White House team. During final edits, the description of the stroke signal was quietly changed from "moderately elevated" to "slightly elevated." Who made that change? Nobody knows. The language softened, the edit went unattributed, and the public remained in the dark.

The pattern is consistent. Senate investigators previously established that Biden officials also downplayed the risk of vaccine-induced myocarditis and kept that from the public. This wasn't a one-time failure. It was a system.

The fallout from that kind of institutional betrayal is hard to overstate. According to the Kaiser Family Foundation, fewer than half of all Americans now trust the CDC and FDA to operate free from political or special-interest influence.
Cool story, bro. PM me your tits
 
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