Recent Posts
-
This Blogger needs your help to shine a light on grift, graft and pagan witchcraft in science
-
AI finds the legal bombs: The Blob can’t hide things in 1,000 page OmniPork bills anymore
-
Saturday
-
Friday
-
Surprise! We thought trees emitted methane, but instead they absorb it… (What else don’t we know?)
-
Blockbuster honesty: Expert modeler admits they can’t predict extreme events, El Nino, tipping points, rain or river flows
-
Thursday
-
Anxious NOAA scientists feel Trump’s “target on their back”, drop climate change and call it “air-quality”
-
Wednesday
-
Tuesday
-
Europe Wind power “sh*t situation”: Norway vows to cut cables, Sweden “furious” blames Germany
-
Monday
-
Sunday
-
Moderna halts RSV mRNA trial abruptly as vaccinated children twice as likely to get a severe illness
-
Saturday
-
The Opposition’s nuclear plan saves $260 billion, but it’s still 53% renewable
-
Friday
-
For years the CCP has been sending millions to US universities and NGOs to promote Green Energy
-
Thursday
-
Denmark offers largest offshore wind area for auction, but no one bids anything
|
By Jo Nova
It’s a war on The Blob
Trump has endorsed the man they call the anti-vax conspiracy theorist, the one who wrote the book accusing Anthony Fauci of abusing his power for thirty years. (Something Fauci has not sued him for). RFK Jr has relentlessly criticized the CDC, the FDA, and the NIH for more than twenty years, while they’ve mocked him and refused to give him the data, and now he’ll be in charge of them.
This move has been telegraphed for months, and happened exactly as promised, yet shares in vaccine makers GSK, Moderna, Pfizer, and Sanofi fell three to seven percent today anyhow.
It’s a moment of master trolling. The far right extremist Donald Trump has put a Democrat environmentalist in charge of health and told him to “Go wild”.
https://www.theguardian.com/us-news/2024/nov/14/trump-administration-rfk-criticisms
Despite the so-called “controversy” of this decision, everyone seems to have forgotten that only six weeks ago the former head of the CDC, Robert Redfield, admitted that Trump and Kennedy were both right. In a blockbuster Newsweek article, the man Kennedy had criticized said:
“All three of the principal health agencies suffer from agency capture”. “A large portion of the […]
By Jo Nova
Vivek Ramaswamy worked in the pharmaceutical industry. Now that he’s free to speak, he distills the utter corruption of the FDA in under four minutes, it is beyond redemption, rotten to the core. “That’s’s why I favor a dramatic drastic gutting of the FDA…” — he says. Exactly…
He’s a great speaker:
Seriously… How do you argue this? He’s right. https://t.co/pQHjerGzLl
— Shawn Ryan (@ShawnRyan762) August 29, 2023
From his Twitter feed: “The corrupt FDA says you don’t have the right to even *try* medicines that haven’t been through 10+ years of testing, yet the government *mandated* Covid vaccines that sailed through FDA approval in less than 1 year. You can’t believe both things at once. Countless FDA regulations and actions are hypocritical, harmful & unconstitutional. I will rescind them accordingly, using the Supreme Court’s holding in West Virginia vs. EPA as my legal basis for doing so. For years I was coached by industry veterans not to speak out against FDA. It’s well known that if you anger FDA, they will punish you by blackballing review of your drug review applications. “FDA never forgets” is a quietly-whispered, well-known pharma industry adage. […]
By Jo Nova
Thirteen remarkable minutes everyone needs to see.
Remarkably, despite the aura of modern space-age medicine — not one childhood vaccine of the 72 that are recommended in the US — has ever been subject to a long term pre-licensing placebo controlled safety trial. Kennedy knows, because he took legal action to get Anthony Fauci to supply one study. After a year of litigation, they admitted they could not provide a single study.
As Kennedy says, he’s not anti-vaccination, he just wants good safety studies — something everyone wants, except maybe certain shareholders.
“Calling people “anti-vaxxers” is a way of silencing them.”
So, for decades, our highly trained doctors have been injecting babies and children with medicines that we didn’t test properly.
The four big companies that make vaccines … Merck, Sanofi, Glaxo and Pfizer, have paid over $35 billion dollars in criminal penalties in the last decade, for lying to doctors, falsifying science, for defrauding regulators…
RF Kennedy Junior’s site is Children’s Health Defense. They have a list of safety studies and controlled trials that use active ingredients in the comparison arm instead of inert placebos like sugar pills. Putting active compounds in both […]
By Jo Nova
The Malhotra-Dowd-Wolf-Shipman event about the Corruption of Medicine in Perth was a smashing success. The crowd of nearly 2,500 was on fire, the speakers were excellent and you can still watch it (and help cover some of the costs) by buying tickets to watch it online. Four hours of some of the best and brightest of humanity.
Fact-of-the-day (for me) was that the Australian TGA (drug approval agency) gets 96% of its budget from the industry it supposedly is a watchdog for. Hello? So when the TGA inexplicably banned the safe ivermectin and hydroxychloroquine options they were, it seems, just doing what any bought-and-paid corporate crony agency would, even if people died. Apparently the government agencies are not just a rubber stamp for profitable drugs, they are the iron mallet to crush the competition too.
Cartoon thanks to Panda at FirstFactCheck
While Australia won the prize for the agency with the Biggest Conflict of Interest, there’s little material difference in the EU, the US or the UK (or Canada). The drug industry funds 89% of the EMA budget in Europe and 86% of […]
By Jo Nova
The insidious vaccine debacle may seem to have come out of nowhere, but pharmaceutical and regulatory rot has been growing for decades.
The story of Zantac, the common heartburn medicine, is both awful and good – it’s awful because one of the most common drugs on the market may have been causing cancers for forty years. It’s good only because the story is finally being told and 70,000 people are suing GlaxoSmithKline (GSK). The “good” here is the hope that some justice might finally be done, and because the public might find out just how ghastly the industrial pharma octopus really is, and how welded it is in the system.
It’s time to burn down the unholy empire of Big Pharma and Big Government and start again.
This is not a case of one bad egg in the system, it’s the story of a system that virtually creates bad eggs
Glaxo was a little company in the 70s that took one of the most popular drugs on the market, Tagamet, tweaked it enough to patent a “better version”, then aggressively out-marketed it, and eventually bought out the companies that made Tagamet to become the $70 billion GlaxoSmithKline […]
By Jo Nova
UPDATE: Pfizer have responded! Wow. They don’t even mention the unwitting informant Jordon Walker, thus suggesting he is one their own. They deny they do Gain of Function or Directed Evolution, but admit “we have conducted research where the original SARS-CoV-2 virus has been used to express the spike protein from new variants of concern.” AND: “In a limited number of cases when a full virus does not contain any known gain of function [GOF] mutations, such virus may be engineered to enable the assessment of antiviral activity in cells”.
Pfizer are admitting to adding GOF mutations, and to mixing the new spike and old nasty virus!
Are they not saying they engineer viruses — starting with the original Wuhan virus and adding the new spike from new “variants of concern”? The new Omicron variants have incredibly well evolved spikes that are so much more infectious than the original variant, but the Omicron virus “in toto” is much less dangerous than the original Wu-Flu. So by mixing the old nasty variant with the new spike, they could be playing with a virus that has the worst of both? How’s that for “potent”?
[…]
By Jo Nova
None of it makes any sense — except for the money
If the CDC puts a particular vaccine on the childhood vaccine schedule Big Pharma automatically is thereafter liability free “forever” for that vaccine. And that may happen in the next 24 hours. So this is a Platinum Jackpot moment for Pharmaceutical shareholders, but makes no medical sense at all. It’s the logical but absurd endpoint of a civilization run on bubble-money. If we print enough money from nothing to capture the agencies, buy off the media, and keep the politicians on a leash, we will get served a Plateful of Stupid. And so it is coming to pass…
Watch Tucker’s face as the good Doctor Makary explains the situation. I mean really, in serious straight tones we’re saying that 50 million American children will be told to take a vaccine that has only been tested on eight mice, for a disease that poses little known threat to them, with a vaccine that isn’t likely to help for long, and which has serious known side-effects, and, by the way, there’s no clinical data to assess. Big Pharma says they’ve done a study, but the data is […]
Written by Jo Nova
A reminder that the dark influence of corruption started decades ago:
It may have seemed like things went off the rails in the last two years, but it couldn’t have been achieved without fifty years of work. The absurdities just felt like they came out of nowhere.
Herbert Ley sounds like a great man. From Wikipedia:
His three years at the FDA came during the time when the FDA grew from an insignificant agency to the key agency protecting consumers; during that time 300 drugs were removed from the market.[4] After he left, Ley stated that he had “constant, tremendous, sometimes unmerciful pressure” from the drug industry and that the drug company lobbyists, combined with the politicians who worked on behalf of their patrons, could bring “tremendous pressure” to bear on him and his staff, to try preventing FDA restrictions on their drugs.
There’s a sad article in Woroni (Canberra) in 1980 lamenting the reach of drug companies. An antibiotic called Panalba had been sold in the US from 1957 generating $18m in revenue for Upjohn. By 1968 30 experts from the National Academy of Science declared that it was harmful and should […]
No one silences experts because they have a great product ‘People are getting bad advice and we can’t say anything.’ Marty Makary M.D., M.P.H. and Tracy Beth Høeg M.D., Ph.D.
Photo by Colin Maynard
Right now, internal critics of these agencies are focused on one issue above all: Why did the FDA and the CDC issue strong blanket recommendations for Covid vaccines in children?
The calls and text messages are relentless. On the other end are doctors and scientists at the top levels of the NIH, FDA and CDC. They are variously frustrated, exasperated and alarmed about the direction of the agencies to which they have devoted their careers.
“It’s like a horror movie I’m being forced to watch and I can’t close my eyes,” one senior FDA official lamented. “People are getting bad advice and we can’t say anything.”
That particular FDA doctor was referring to two recent developments inside the agency. First, how, with no solid clinical data, the agency authorized Covid vaccines for infants and toddlers, including those who already had Covid. And second, the fact that just months before, the FDA bypassed their external experts to […]
Was the data Pfizer sent, really this bad?
If it wasn’t, it should be easy for the FDA and or Pfizer to reply. If it was this extraordinarily rigged to “find” some infinitesimally tiny benefit among the acres of null and even bad results, we have to ask, does anyone care about babies anymore? If the data Pfizer sent is this awful, no one is even trying to hide the corruption. Does the FDA care about its own reputation?
According to Dr Clare Craig (in the video below) — the evidence that Pfizer sent to the FDA is dubious in the extreme: As she tells it — the trial recruited 4,526 children aged from 6 months to 4 years, but as many as 3,000 did not finish the trial. On that basis alone, she says, “the trial should be deemed null and void.” This trial data is so they can get EUA – Emergency Use Authorisation, but they defined severe covid as a raised heartrate and an increased breathing rate — which hardly sounds like an emergency, or something severe. In the end there were only six children age 2 – 4 that had “severe covid” and who were vaccinated […]
Project Veritas has caught an FDA executive on hidden camera admitting that Big Pharma pay hundreds of millions to the agency that decides whether their products get approved for use. He explains that the next goal is annual “recurring” vaccines, mandated. He talked casually about the lack of good research and how the vaccines have not been as effective as they were expecting.
This kind of expose is so important for all the people who find scientific arguments difficult. Everyone understands corruption.
Christopher Cole, an FDA Executive Officer with twenty years experience:
“The drug companies, the food companies, the vaccine companies, they pay us hundreds of millions of dollars a year to hire and keep the reviewers to approve their products.”
“…if they can get every person required to get an annual vaccine, they get a recurring return of money going into their company.”
“Just from everything I’ve heard… they’re not going to Not approve this.”
“My agency overseas vaccines”. “My office clears all the emergency approvals”
Biden wants to innoculate as many people as possible So you’ll have to get an annual shot.
It hasn’t been formally […]
In October the FDA asked the judge to let them have 55 years to release all the data, but now Aaron Siri, a lawyer connected to the FOIA, reports they want to hide some of the data for 75 years.
Mere mortals could lose their jobs and their houses immediately if they won’t take the vax, but something must be pretty bad about the vaccine trial results that both the FDA and Pfizer now want to keep the data hidden until 2096.
Apparently, the FDA have 451,000 pages of information related to their decision to license the Pfizer vaccine. The FDA reviewed all this in just 108 days — which works out to the committee going through 4,176 pages a day. More, if they took weekends off.
Nothing says “Trust us” like hiding the data til 2096.
Try to imagine what circumstances would limit the FDA to 500 pages a month:
They are still using dial up. They still need to read the pages. They are afraid of being put in jail.
Apparently, the FDA or US Food and Drug Administration is not just covering up for Pfizer, but covering it for itself. The FDA is a government […]
Photo by Hakan Nural on Unsplash
The FDA licensed the Pfizer vaccine in August but hasn’t released the data and documents the decision was based on. So lawyers filed a suit against the FDA to make that information fully available to the public.
Aaron Siri, a lawyer at Siri Glimstad explains that the FDA has now asked the judge to allow it to drip-feed out the information at a pace so slow that the complete set won’t be available until 2076.
Remember, the vaccine is totally safe and has astonishing efficacy, right?
Perhaps they need a bigger internet cable.
The FDA promises full transparency for Pfizer Vaccine data “in 55 years time”
by Aaron Siri:
The federal government shields Pfizer from liability. Gives it billions of dollars. Makes Americans take its product. But won’t let you see the data supporting its product’s safety and efficacy. Who does the government work for?
To date, almost three months after it licensed Pfizer’s vaccine, the FDA still has not released a single page. Not one.
Instead, two days ago, the FDA asked a federal judge to give it until 2076 to fully produce this information. […]
Dr Marion Gruber and Dr Phillip Krause were not just at the FDA, they had been there for 30 years and were heading up the teams that decided last week to approve Pfizer for 16 year olds last week.
Two Top FDA Vaccine Regulators Are Set to Depart During a Crucial Period
Noah Weiland and Sharon LaFraniere, New York Times
Gruber and Krause were upset about the Biden administration’s recent announcement that adults should get a coronavirus booster vaccination eight months after they received their second shot, according to people familiar with their thinking.
Neither believed there was enough data to justify offering booster shots yet, the people said, and both viewed the announcement, amplified by President Joe Biden, as pressure on the FDA to quickly authorize them.
They are worried about that Israeli data showing people vaccinated in January only had 16% protection left in July.
White House officials have stressed that the plan for Americans to start receiving boosters next month was uniformly endorsed by the most senior federal health officials, including Dr. Janet Woodcock, the acting FDA commissioner. They have described the need to develop a booster plan as […]
The FDA has launched a marketing program to rebrand the Wonder Drug from Japan as just a horse paste and thus bury the 3.8 billion doses given to very non-horsey humans, many of whom were in Subsaharan Africa. On another day this would be a hideously racist. When do 200 million Africans count for nothing?
The FDA may hope to save people from self-medication accidents, but will regret telling a half-truth-soup and burning up more of what’s left in their trust-bucket. After all, they want the public to trust them with their lives, but it only takes one eye opening conversation to undo years of propaganda. If the FDA are not mentioning that something like 200 million humans use Ivermectin each and every year — what else are they hiding? That it won a Nobel Prize and costs $1 a day?
The FDA and the Guardian and co, are training readers to mock anyone who even asks about Ivermectin. It’s the old Argumentum By Derision again. The tool of bullies, not scientists.
Martin Pengelly at The Guardian got the message the FDA was sending:
Ahead of full US authorisation of the Pfizer coronavirus vaccine, the federal Food […]
The most popular drug with doctors all over the world will seemingly now not even be allowed in the US for Covid related treatment: HCQ No Longer Approved Even a Little for COVID-19
Molly Walker, MedPage
The FDA rescinded its emergency use authorization (EUA) of hydroxychloroquine (HCQ) to treat COVID-19 patients, citing concerns about efficacy and risks associated with its use, and saying the drug no longer meets the criteria for an EUA, the agency said on Monday.
Moreover, the FDA now says the benefits of the drug “no longer outweigh the potential risks,” citing the serious cardiac adverse events associated with the drug.
Comments underneath reveal just how contested this will be.
It’s a strange situation where patients in many poorer nations are being offered drugs that patients won’t be able to get in the richest nation in the world:
Substantial fractions of physicians treating Covid-19 patients in Europe and elsewhere report use of HCQ+AZ: 72% in Spain, 49% in Italy, 41% in Brazil, 39% in Mexico, 28% in France, 23% in the US, 17% in Germany, 16% in Canada, 13% in the UK (45), much of the non-US use […]
|
JoNova A science presenter, writer, speaker & former TV host; author of The Skeptic's Handbook (over 200,000 copies distributed & available in 15 languages).
Jo appreciates your support to help her keep doing what she does. This blog is funded by donations. Thanks!
Follow Jo's Tweets To report "lost" comments or defamatory and offensive remarks, email the moderators at: support.jonova AT proton.me
Statistics
The nerds have the numbers on precious metals investments on the ASX
|
Recent Comments