Dr Strangetroll : or how I learned to stop arguing and be amused by the intransigence
- Thread starter Shale MacGregor
- Start date
MurphyGuy
It just needs a bigger hammer
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That's cool.. strange joke.. but I'm good.
I was curious to know what the leading causes were myself.. not something I ever gave any thought about..
As I said, I seem to be immune, so have never needed vaccines or drugs.
But my concern is that the FDA is rushing through approval on vaccines that have not been fully tested, and the pharmaceutical companies are again assuring everyone they're safe.
I went to school in England in the very early 60's, and two of my classmates not only suffered from the effects of thalidomide, but also had to go through their childhood with the taunts of the other children.
I'll take my chances, and not get vaccinated.
Eric Clapton says he had a "disastrous" reaction to COVID-19 vaccine after experiencing side-effects
Eric Clapton has shared his vaccination experience, calling his reactions "disastrous" and criticising the so-called "propaganda" promoting its safety.
www.nme.com
I stand corrected.
BMcL
Solar Enthusiast
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Apparently Pfizer has a good reason to hide the adverse reactions to their vaccine :
Court Orders FDA To Comply With FOIA and Release Information On Pfizer Vaccine – First Batch of Documents Shows Over 1,200 Vaccine Deaths WITHIN FIRST 90 DAYS
https://www.thegatewaypundit.com ^ | DECEMBER 2, 2021 | Julian Conradson
The Food and Drug Administration (FDA) released the first batch of documents related to Pfizer’s Covid-19 vaccine after a federal judge ordered that they must comply with a massive Freedom of Information Act (FOIA) request that was filed by a government accountability group called Public Health and Medical Professionals for Transparency.
The esteemed group of more than 30 professors and scientists asked the federal government to share any and all data that factored into the agency’s hasty decision to grant Pfizer’s experimental mRNA vaccine an emergency use authorization (EUA) – which amounts to a trove of over 329,000 documents.
In a shameless effort to bury the information, the FDA challenged the FOIA request in court. After the agency was told that it must turn over the documents, Justice Department lawyers representing the FDA asked a federal judge to allow them an unthinkable 55 years to process the request, saying that they would be able to release just 500 pages a month.
…
A motion that was also filed by the same group of doctors and scientists is currently pending in federal court that would force the FDA to expedite processing and releasing these documents.
Meanwhile, the FDA still has to comply with the original order to begin turning over documents. Lo and behold, the first release is a bombshell.
According to an official Pfizer document that is titled Cumulative Analysis of Post-Authorization Adverse Event Records Reports, in just the first 90 days of the vaccine’s roll out under the FDA’s EUA – from December 1st. 2020 – February 28th, 2021 – there were TENS OF THOUSANDS of reported adverse reactions, including OVER 1200 DEATHS.
The report only included adverse events to the vaccine that researchers considered “serious cases,” there were thousands more submissions that were left out of this data.
meaninginhistory.substack.com
Court Orders FDA To Comply With FOIA and Release Information On Pfizer Vaccine – First Batch of Documents Shows Over 1,200 Vaccine Deaths WITHIN FIRST 90 DAYS
https://www.thegatewaypundit.com ^ | DECEMBER 2, 2021 | Julian Conradson
The Food and Drug Administration (FDA) released the first batch of documents related to Pfizer’s Covid-19 vaccine after a federal judge ordered that they must comply with a massive Freedom of Information Act (FOIA) request that was filed by a government accountability group called Public Health and Medical Professionals for Transparency.
The esteemed group of more than 30 professors and scientists asked the federal government to share any and all data that factored into the agency’s hasty decision to grant Pfizer’s experimental mRNA vaccine an emergency use authorization (EUA) – which amounts to a trove of over 329,000 documents.
In a shameless effort to bury the information, the FDA challenged the FOIA request in court. After the agency was told that it must turn over the documents, Justice Department lawyers representing the FDA asked a federal judge to allow them an unthinkable 55 years to process the request, saying that they would be able to release just 500 pages a month.
…
A motion that was also filed by the same group of doctors and scientists is currently pending in federal court that would force the FDA to expedite processing and releasing these documents.
Meanwhile, the FDA still has to comply with the original order to begin turning over documents. Lo and behold, the first release is a bombshell.
According to an official Pfizer document that is titled Cumulative Analysis of Post-Authorization Adverse Event Records Reports, in just the first 90 days of the vaccine’s roll out under the FDA’s EUA – from December 1st. 2020 – February 28th, 2021 – there were TENS OF THOUSANDS of reported adverse reactions, including OVER 1200 DEATHS.
The report only included adverse events to the vaccine that researchers considered “serious cases,” there were thousands more submissions that were left out of this data.
Catching Up With Covid 12/2/21
I have two items that I want to paste in, but first … Ominous Omicron. If you’ve been following the news today, you’ll have noticed three things: More and more cases of Ominous Omicron are popping up; Every case I’ve heard of has occurred in fully vaxxed individuals; and
meaninginhistory.substack.com
We went through this in detail above with Bob B's post. What you say above is in part a gross mischaracterization and part outright lie. You have mental issues.Apparently Pfizer has a good reason to hide the adverse reactions to their vaccine :
Court Orders FDA To Comply With FOIA and Release Information On Pfizer Vaccine – First Batch of Documents Shows Over 1,200 Vaccine Deaths WITHIN FIRST 90 DAYS
https://www.thegatewaypundit.com ^ | DECEMBER 2, 2021 | Julian Conradson
The Food and Drug Administration (FDA) released the first batch of documents related to Pfizer’s Covid-19 vaccine after a federal judge ordered that they must comply with a massive Freedom of Information Act (FOIA) request that was filed by a government accountability group called Public Health and Medical Professionals for Transparency.
The esteemed group of more than 30 professors and scientists asked the federal government to share any and all data that factored into the agency’s hasty decision to grant Pfizer’s experimental mRNA vaccine an emergency use authorization (EUA) – which amounts to a trove of over 329,000 documents.
In a shameless effort to bury the information, the FDA challenged the FOIA request in court. After the agency was told that it must turn over the documents, Justice Department lawyers representing the FDA asked a federal judge to allow them an unthinkable 55 years to process the request, saying that they would be able to release just 500 pages a month.
…
A motion that was also filed by the same group of doctors and scientists is currently pending in federal court that would force the FDA to expedite processing and releasing these documents.
Meanwhile, the FDA still has to comply with the original order to begin turning over documents. Lo and behold, the first release is a bombshell.
According to an official Pfizer document that is titled Cumulative Analysis of Post-Authorization Adverse Event Records Reports, in just the first 90 days of the vaccine’s roll out under the FDA’s EUA – from December 1st. 2020 – February 28th, 2021 – there were TENS OF THOUSANDS of reported adverse reactions, including OVER 1200 DEATHS.
The report only included adverse events to the vaccine that researchers considered “serious cases,” there were thousands more submissions that were left out of this data.
Catching Up With Covid 12/2/21
I have two items that I want to paste in, but first … Ominous Omicron. If you’ve been following the news today, you’ll have noticed three things: More and more cases of Ominous Omicron are popping up; Every case I’ve heard of has occurred in fully vaxxed individuals; and
It is in the other thread but discussed in detail. I have read the document now 4x. If anyone serious has questions that did not get answered by the other thread I will be happy to answer them.
Yes, that party is pretty clear in the data. It will get you after two-dose vaccine also but not as bad as a natural infection. All very early and limited data though. How the booster and omicron match up remains to be seen but that clearly is the strongest position one can be in together with an N95 mask.
Omicron-----------get a booster. This is airborne transmission across a hallway with closed doors.
1.
@GuHaogao
& colleagues report on an apparent case of #Omicron transmission in a Hong Kong quarantine hotel. Traveler from South Africa tests positive 2 days after arrival; traveler from Canada who is located directly across the hall tests positive 4 days later. 2. Canadian traveler was 7 days into quarantine when he tested positive. Viral sequences were compared; almost identical. Both travelers were twice vaxed with Pfizer in the spring. Surveillance footage showed neither left their room, only opening doors for food, testing.
"Airborne transmission across the corridor is the most probable mode of transmission," the University of Hong Kong researchers (including
@bencowling88
) report in
@CDC_EIDjournal
. https://wwwnc.cdc.gov/eid/article/28/2/21-2422_article
1.
@GuHaogao
& colleagues report on an apparent case of #Omicron transmission in a Hong Kong quarantine hotel. Traveler from South Africa tests positive 2 days after arrival; traveler from Canada who is located directly across the hall tests positive 4 days later. 2. Canadian traveler was 7 days into quarantine when he tested positive. Viral sequences were compared; almost identical. Both travelers were twice vaxed with Pfizer in the spring. Surveillance footage showed neither left their room, only opening doors for food, testing.
"Airborne transmission across the corridor is the most probable mode of transmission," the University of Hong Kong researchers (including
@bencowling88
) report in
@CDC_EIDjournal
. https://wwwnc.cdc.gov/eid/article/28/2/21-2422_article
MurphyGuy
It just needs a bigger hammer
- Joined
- May 20, 2020
- Messages
- 4,129
Apparently Pfizer has a good reason to hide the adverse reactions to their vaccine :
Court Orders FDA To Comply With FOIA and Release Information On Pfizer Vaccine – First Batch of Documents Shows Over 1,200 Vaccine Deaths WITHIN FIRST 90 DAYS
https://www.thegatewaypundit.com ^ | DECEMBER 2, 2021 | Julian Conradson
The Food and Drug Administration (FDA) released the first batch of documents related to Pfizer’s Covid-19 vaccine after a federal judge ordered that they must comply with a massive Freedom of Information Act (FOIA) request that was filed by a government accountability group called Public Health and Medical Professionals for Transparency.
The esteemed group of more than 30 professors and scientists asked the federal government to share any and all data that factored into the agency’s hasty decision to grant Pfizer’s experimental mRNA vaccine an emergency use authorization (EUA) – which amounts to a trove of over 329,000 documents.
In a shameless effort to bury the information, the FDA challenged the FOIA request in court. After the agency was told that it must turn over the documents, Justice Department lawyers representing the FDA asked a federal judge to allow them an unthinkable 55 years to process the request, saying that they would be able to release just 500 pages a month.
…
A motion that was also filed by the same group of doctors and scientists is currently pending in federal court that would force the FDA to expedite processing and releasing these documents.
Meanwhile, the FDA still has to comply with the original order to begin turning over documents. Lo and behold, the first release is a bombshell.
According to an official Pfizer document that is titled Cumulative Analysis of Post-Authorization Adverse Event Records Reports, in just the first 90 days of the vaccine’s roll out under the FDA’s EUA – from December 1st. 2020 – February 28th, 2021 – there were TENS OF THOUSANDS of reported adverse reactions, including OVER 1200 DEATHS.
The report only included adverse events to the vaccine that researchers considered “serious cases,” there were thousands more submissions that were left out of this data.
Catching Up With Covid 12/2/21
I have two items that I want to paste in, but first … Ominous Omicron. If you’ve been following the news today, you’ll have noticed three things: More and more cases of Ominous Omicron are popping up; Every case I’ve heard of has occurred in fully vaxxed individuals; and
The gatewaypundant is being sued! ROFLMAO.
You can say goodbye to that fake news website within the next year or so. They better hope I'm not on the Jury.
BMcL
Solar Enthusiast
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- Sep 5, 2021
- Messages
- 834
LOL you've proved that for sure
The conditions that set the table for Omicron in the hardest hit part of South Africa are : 1. Low vaccination rate 2. Low current rate of Delta 3. high level of reliance on natural immunity rather than masking etc. The section of the US this most resembles right now is the south eastern US.
Pfizer, Moderna, J&J, and literally every other pharma company have lost billions of dollars in lawsuits for doing things that they knew were illegal and dangerous. Im sure they are just as trustworthy as the Pundit though....
Pfizer: Corporate Rap Sheet | Corporate Research Project
Pfizer By Philip Mattera
Merck: Corporate Rap Sheet | Corporate Research Project
Merck By Philip Mattera For decades Merck had a sterling reputation for integrity and high-quality research in a pharmaceutical industry whose other major players were often regarded in a much less favorable light. For a long time Merck also avoided the merger mania that afflicted its rivals.
Johnson & Johnson: Corporate Rap Sheet | Corporate Research Project
Johnson & Johnson by Philip Mattera
You never will be for the same reason BMcL will never be on the jury for big pharma. You two are different sides of the same coin.
Strong disagree. There is an objective truth.
You obviously fail to understand how the legal system works as well as bias. They both are on the extremes, as are you, which makes your disagreeing irrelevant as well.
Furthermore, anyone with this opinion is trash. As such I have relegated you to the trash pile and as far as I am concerned you opinions and speech have no meaningful value in civil or any other discourse.
I practiced law for thirty (30) years. Graduated from the University of Notre Dame Law School in 1981. You?
I just ended the law career of a lawyer that was legal council for the not for profit I began sitting on less than a year ago.
There are lots of garbage people that do garbage work in professions they have tons of "experience in". You may well be one of them.
A good start would be learning how to spell "counsel".
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