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They had to admit in court that their fact checkers are nothing but opinion. I always give them **** on Instagram for it everytime I see a flagged post.
Covid Vaccine
- Thread starter jitter77
- Start date
They had to admit in court that their fact checkers are nothing but opinion. I always give them **** on Instagram for it everytime I see a flagged post.
More please. More.
Conservative public interest advocacy group Defending the Republic (DTR) has obtained almost 15,000 pages of Moderna’s COVID-19 vaccine clinical trial data, claiming the data show an “utter lack of thoroughness” of the trials and calls the vaccine’s safety into “serious doubt.”
As a result of successful Freedom of Information Act (FOIA) litigation against the U.S. Food and Drug Administration (FDA), the group recently announced it had obtained—and is releasing—nearly 15,000 pages of documents relating to testing and adverse events associated with “Spikevax,” Moderna’s COVID-19 vaccine.
Since 2022, the group has been involved in litigation against the FDA relating to the production of data submitted by Moderna in support of its application to federal regulators for approval of its vaccine.
As a result, the FDA agreed to produce around 24,000 pages of the Moderna records by the end of this year, with the 15,000 pages being the first instalment.
The records, some of which relate to adverse events related to the vaccine, include important information related to the safety profile of Spikevax, which was first authorized for emergency use in the United States in December 2020 and in January 2022 received full approval for adults.
“The public can be assured that Spikevax meets the FDA’s high standards for safety, effectiveness and manufacturing quality required of any vaccine approved for use in the United States,” Acting FDA Commissioner Dr. Janet Woodcock said in a statement earlier this year.
But the new data call this view into question. The advocacy group says that the tens of thousands of pages of clinical trial data released by the FDA supports the conclusion that there is “serious doubt” about both the safety of Spikevax and the FDA’s standards for approval.
Neither Moderna nor the FDA immediately responded to a request for comment.
The documents obtained as part of the group’s litigation against the FDA are the first significant release of data from Moderna’s COVID-19 clinical trials.
The studies reveal the causes of deaths, serious adverse events, and instances of neurological disorders potentially associated with Spikevax.
One of the key takeaways from the documents is that many of those who died after receiving the Moderna vaccine were not given an autopsy.
“According to one study, 16 individuals died after being administered the Moderna vaccine. The study’s authors indicated that out of those 16 deaths, only two autopsies were performed, five of the dead were not autopsied, and the autopsy status of nine of the dead was ‘unknown,’” DTR said in a statement.
“Yet this did not stop those running these ‘studies’ from concluding, despite the absence of evidence, that the Moderna vaccine was not related to these deaths,” the group added.
As an example, the group gave the case of a 56-year-old woman who experienced ‘sudden death’ 182 days after receiving the second dose of the Moderna vaccine.
“The cause of death was unknown, and no autopsy was conducted. It seems they purposely decided not to investigate suspicious deaths in case the Moderna vaccine might be the cause,” the group stated.
There were also numerous examples in the clinical trial data of participants diagnosed with post-vaccination Bell’s Palsy and Shingles, with numerous vaccinated trial participants seeing the onset of Shingles less than 10 days after getting the shot.
The studies also showed that there were a number of serious adverse events noted in the vaccinated groups, with a number of participants experiencing heart attacks, pulmonary embolisms, and spontaneous miscarriages.
Overall, the group concludes that the 15,000 pages of data create “serious doubt concerning the safety of the Moderna vaccine and the FDA’s standards and approval of the Moderna vaccine.”
The 15,000 pages or so of data released by DTR, all of which can be found here, add to the growing body of evidence suggesting that the COVID-19 vaccines may not be as safe as advertised.
In a May 9 decision hailed as a win for transparency by the lawyer representing the plaintiffs (the parents of a child injured by a COVID-19 vaccine) in a lawsuit (pdf) against the FDA, the agency was ordered to produce the data on Moderna’s vaccine for adults and Pfizer’s for children about 10 times faster than the agency wanted.
“Democracy dies behind closed doors,” is how U.S. District Judge Mark Pittman opened his order (pdf), which requires the FDA to produce the data on Moderna’s and Pfizer’s COVID-19 vaccines at an average rate of at least 180,000 pages per month.
The FDA had argued it would be “impractical” to release the estimated 4.8 million pages at more than between 1,000 and 16,000 pages per month, which would have taken at least 23.5 years.
The January 2022 order (pdf), also issued by Pittman, forced the FDA to produce all its data on Pfizer’s COVID-19 vaccine for those aged 16 and older at a rate of 55,000 pages per month, or much faster than the 75 years the agency had sought.
“That production should be completed in a few more months,” Siri said in a statement, referring to the earlier Pfizer data for those aged 16 and up.
The latest order requires the FDA to produce all of its data on Pfizer’s COVID-19 vaccine for 12- to 15-year-olds (and Moderna’s product for adults) by June 31, 2025.
FDA officials didn’t respond to a request for comment on the ruling.
‘Serious Doubt’ About COVID-19 Vaccine Safety After Forced Release of 15,000 Pages of Clinical Trial Data: Legal NGO
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www.theepochtimes.com
Conservative public interest advocacy group Defending the Republic (DTR) has obtained almost 15,000 pages of Moderna’s COVID-19 vaccine clinical trial data, claiming the data show an “utter lack of thoroughness” of the trials and calls the vaccine’s safety into “serious doubt.”
As a result of successful Freedom of Information Act (FOIA) litigation against the U.S. Food and Drug Administration (FDA), the group recently announced it had obtained—and is releasing—nearly 15,000 pages of documents relating to testing and adverse events associated with “Spikevax,” Moderna’s COVID-19 vaccine.
Since 2022, the group has been involved in litigation against the FDA relating to the production of data submitted by Moderna in support of its application to federal regulators for approval of its vaccine.
As a result, the FDA agreed to produce around 24,000 pages of the Moderna records by the end of this year, with the 15,000 pages being the first instalment.
The records, some of which relate to adverse events related to the vaccine, include important information related to the safety profile of Spikevax, which was first authorized for emergency use in the United States in December 2020 and in January 2022 received full approval for adults.
“The public can be assured that Spikevax meets the FDA’s high standards for safety, effectiveness and manufacturing quality required of any vaccine approved for use in the United States,” Acting FDA Commissioner Dr. Janet Woodcock said in a statement earlier this year.
But the new data call this view into question. The advocacy group says that the tens of thousands of pages of clinical trial data released by the FDA supports the conclusion that there is “serious doubt” about both the safety of Spikevax and the FDA’s standards for approval.
Neither Moderna nor the FDA immediately responded to a request for comment.
More Details
DTR filed its FOIA lawsuit after the FDA rejected requests to produce the Moderna COVID-19 records, justifying its decision by claiming there was no pressing need for the public to review the information.The documents obtained as part of the group’s litigation against the FDA are the first significant release of data from Moderna’s COVID-19 clinical trials.
The studies reveal the causes of deaths, serious adverse events, and instances of neurological disorders potentially associated with Spikevax.
One of the key takeaways from the documents is that many of those who died after receiving the Moderna vaccine were not given an autopsy.
“According to one study, 16 individuals died after being administered the Moderna vaccine. The study’s authors indicated that out of those 16 deaths, only two autopsies were performed, five of the dead were not autopsied, and the autopsy status of nine of the dead was ‘unknown,’” DTR said in a statement.
“Yet this did not stop those running these ‘studies’ from concluding, despite the absence of evidence, that the Moderna vaccine was not related to these deaths,” the group added.
As an example, the group gave the case of a 56-year-old woman who experienced ‘sudden death’ 182 days after receiving the second dose of the Moderna vaccine.
“The cause of death was unknown, and no autopsy was conducted. It seems they purposely decided not to investigate suspicious deaths in case the Moderna vaccine might be the cause,” the group stated.
There were also numerous examples in the clinical trial data of participants diagnosed with post-vaccination Bell’s Palsy and Shingles, with numerous vaccinated trial participants seeing the onset of Shingles less than 10 days after getting the shot.
The studies also showed that there were a number of serious adverse events noted in the vaccinated groups, with a number of participants experiencing heart attacks, pulmonary embolisms, and spontaneous miscarriages.
Overall, the group concludes that the 15,000 pages of data create “serious doubt concerning the safety of the Moderna vaccine and the FDA’s standards and approval of the Moderna vaccine.”
The 15,000 pages or so of data released by DTR, all of which can be found here, add to the growing body of evidence suggesting that the COVID-19 vaccines may not be as safe as advertised.
FDA Ordered to Speed Up Release of COVID-19 Data
Elsewhere, a federal judge in Texas ordered the FDA to make public data it relied on to license COVID-19 vaccines at an accelerated rate, requiring all documents to be made public by mid-2025 rather than, as the FDA wanted, over the course of about 23.5 years.In a May 9 decision hailed as a win for transparency by the lawyer representing the plaintiffs (the parents of a child injured by a COVID-19 vaccine) in a lawsuit (pdf) against the FDA, the agency was ordered to produce the data on Moderna’s vaccine for adults and Pfizer’s for children about 10 times faster than the agency wanted.
“Democracy dies behind closed doors,” is how U.S. District Judge Mark Pittman opened his order (pdf), which requires the FDA to produce the data on Moderna’s and Pfizer’s COVID-19 vaccines at an average rate of at least 180,000 pages per month.
The FDA had argued it would be “impractical” to release the estimated 4.8 million pages at more than between 1,000 and 16,000 pages per month, which would have taken at least 23.5 years.
The January 2022 order (pdf), also issued by Pittman, forced the FDA to produce all its data on Pfizer’s COVID-19 vaccine for those aged 16 and older at a rate of 55,000 pages per month, or much faster than the 75 years the agency had sought.
“That production should be completed in a few more months,” Siri said in a statement, referring to the earlier Pfizer data for those aged 16 and up.
The latest order requires the FDA to produce all of its data on Pfizer’s COVID-19 vaccine for 12- to 15-year-olds (and Moderna’s product for adults) by June 31, 2025.
FDA officials didn’t respond to a request for comment on the ruling.
Let's just wait until we hear what Trog has to say about this.
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it’s Trump’s fault. The noble drug companies all said they needed time but Trump demanded operation warp speed and forced them to go ahead.
That’s the next narrative.
Funny that the Dems were demanding a vaccine, then we got one and they were saying it was untested and dangerous, then Biden got "elected" and suddenly it was mandatory.
Republican vaccine bad.
Democrat vaccine good.
All, perfectly normal in the "new normal"
Goodwin, a 10th-year veteran who signed with the Browns during free agency, said he began experiencing discomfort in his legs and slight shortness of breath during organized team activities in the spring, and a check-up revealed the blood clots in his legs and lungs.
Browns declare non-football illness to WR Marquise Goodwin
Goodwin will miss the start of training camp due to blood clots
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www.clevelandbrowns.com
Goodwin, a 10th-year veteran who signed with the Browns during free agency, said he began experiencing discomfort in his legs and slight shortness of breath during organized team activities in the spring, and a check-up revealed the blood clots in his legs and lungs.
Lol. Da browns.
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"We are pleased to announce Marquise Goodwin does NOT have a staph infection."
- Da Clowns
Maybe not staph but he‘s a Brown, so he caught the ghey. The ‘50s video that Booted posted in the tranny thread taught us that.
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“just wait” that’s what Tim said about the vaccine a couple years ago… I’m still waiting. And I say it’s the Epoch Times for chrissake.Loading…
healthfeedback.org
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healthfeedback.org
Not a peep out of Tim.
I think you finally put him in his place!!!
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Ron, the vaccines from pFizer and Moderna were horrible, damaging more than the good that was hoped fir, while they siphoned over $200 Billion from governments.
It was all a hoax, perpetrated by genocidal maniacs hidden by the US government, brought to you by the same folks proposing continual war, globally.
True, however at the time if Trump had slowed down on that deal the entire media would have plastered us 24/7 with "Trump Wants To Kill People!!!"
My family all got Moderna with no ill effects except for my sister, whose problems I have detailed here before. My wife and I both got Covid anyway.
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I wonder if Bronny was vaxxed?
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I can almost guarantee it.
LeBron was a huge proponent of it back when it was introduced.
Plus he's all kinds of tied to Chinese government.
Come on guys. Clearly this kid was unfit, lazy, ate like ****, poor family genetics that caused this 18 yr old to have heart attack.
Clearly.
Clearly.
****. Down what, 50-60 lbs?
So lets revisit some stuff:
A. Virtually every early educated guess based off of the results from the very early cruise boat quarantines held true…
-about three to four times deadlier than the regular flu.
-Highly transmissible and an aerosol.
-Most infections asymptomatic or extremely mild. Mostly deadly to old and ill people like virtually every other respiratory disease.
-Virtually harmless to anyone under 50. -Extremely harmless to anyone under 18.
B. It absolutely was an accidental release from the wuhan lab. It was never even possible to be a natural occurrence… it’s known that segments of the virus were from a patented man made viral product from a Canadian lab. An intentional release doesn’t jive with the initial crazy Chinese response and would have been likely done in a more high traffic area.
C. The death rates were spiked high based on how certain countries deal with calculating such figures .. ours in particular was spiked higher by the CDC trying to convince people that it was serious by intentionally inflating numbers even higher completely illogically and actual deaths caused by misuse of invasive respirators… typical death rate should have been between 0.066% and 0.080% and almost exclusively in the over 65 crowd…
D. The way they did the approvals for these vaccines was dangerous and stupid because of political considerations… both sides are at fault. People died and the overall impact will not be known for years… we are probably fortunate that the deadly side effects were relatively low compared to some nightmare scenarios
A. Virtually every early educated guess based off of the results from the very early cruise boat quarantines held true…
-about three to four times deadlier than the regular flu.
-Highly transmissible and an aerosol.
-Most infections asymptomatic or extremely mild. Mostly deadly to old and ill people like virtually every other respiratory disease.
-Virtually harmless to anyone under 50. -Extremely harmless to anyone under 18.
B. It absolutely was an accidental release from the wuhan lab. It was never even possible to be a natural occurrence… it’s known that segments of the virus were from a patented man made viral product from a Canadian lab. An intentional release doesn’t jive with the initial crazy Chinese response and would have been likely done in a more high traffic area.
C. The death rates were spiked high based on how certain countries deal with calculating such figures .. ours in particular was spiked higher by the CDC trying to convince people that it was serious by intentionally inflating numbers even higher completely illogically and actual deaths caused by misuse of invasive respirators… typical death rate should have been between 0.066% and 0.080% and almost exclusively in the over 65 crowd…
D. The way they did the approvals for these vaccines was dangerous and stupid because of political considerations… both sides are at fault. People died and the overall impact will not be known for years… we are probably fortunate that the deadly side effects were relatively low compared to some nightmare scenarios
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Glad he's going to be ok.
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Thank God for the shot, since it means we won't get ...
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The cruise ship is particularly interesting given a relatively isolated environment and the ability to study both short- and long-term impacts if any of the passengers continued to be monitored/studied over time.
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