Post by the Scribe on Jan 2, 2023 9:08:02 GMT
Has there ever been a study on why those who are affected negatively had those effects or why they died? Some genetic cause? Blood type? Race? etc. I don't ever hear the why of it. Only the how.
Reanalysis of mRNA trial data
Dr. John Campbell
2.61M subscribers
Share
685,172 views Dec 30, 2022
Swine flu vaccine (1976), 1 serious event per 100,000 vaccinees, Vaccine withdrawn
Rotavirus vaccine Rotashield, (1999),1 to 2 serious events per 10,000 vaccinees, Vaccine withdrawn
Covid mRNA vaccines, 1 serious event per 800 vaccinees, Vaccine officially promoted
Serious adverse events of special interest following mRNA COVID-19 vaccination in randomized trials in adults
pubmed.ncbi.nlm.nih.gov/36055...
Free full text available
www.ncbi.nlm.nih.gov/pmc/arti...
Why We Question the Safety Profile of mRNA COVID-19 Vaccines
(Robert M Kaplan and Sander Greenland)
sensiblemed.substack.com/p/wh...
Using publicly available data from Pfizer and Moderna studies,
we found one serious adverse event for each 800 vaccinees.
That translates to about 1,250 serious events for each million vaccine recipients.
US, Spain, Australia
Study to evaluate serious adverse events of special interest observed in mRNA COVID-19 vaccine trials.
Secondary analysis of serious adverse events reported in the placebo-controlled, phase III randomized clinical trials,
of Pfizer and Moderna mRNA COVID-19 vaccines
Results
Pfizer and Moderna mRNA COVID-19 vaccines were associated with an excess risk of serious adverse events of special interest
Pfizer
10.1 per 10,000 vaccinated over placebo baselines of 17.6
Moderna
15.1 per 10,000 vaccinated over placebo baseline of 42.2
Combined, the mRNA vaccines
Associated with an excess risk of serious adverse events of special interest of 12.5 per 10,000 vaccinated
Pfizer trial
Pfizer vaccine group
52 serious AESI (27.7 per 10,000) were reported
Pfizer placebo group
33 serious AESI (17.6 per 10,000) were reported
36 % higher risk of serious adverse events in the vaccine group
Risk difference 18.0 per 10,000 vaccinated
Moderna trial
Moderna trial, vaccine group
87 serious AESI (57.3 per 10,000) were reported
Moderna trial, placebo group
64 serious AESI (42.2 per 10,000) were reported
6 % higher risk of serious adverse events in the vaccine group
Risk difference 7.1 per 10,000 vaccinated
Discussion
The excess risk of serious adverse events found in our study points to the need for formal harm-benefit analyses,
particularly those that are stratified according to risk of serious COVID-19 outcomes.
These analyses will require public release of participant level datasets.
Full transparency of the COVID-19 vaccine clinical trial data is needed,
to properly evaluate these questions.
Unfortunately, as we approach 2 years after release of COVID-19 vaccines,
participant level data remain inaccessible.
Level of adverse reactions in the past
The 1976 swine flu vaccine
Small increased risk of Guillain-Barré Syndrome
The increased risk was approximately 1 additional case of GBS for every 100,000 people who got the swine flu vaccine.
When over 40 million people were vaccinated against swine flu,
federal health officials decided that the possibility of an association of GBS with the vaccine, however small,
necessitated stopping immunization until the issue could be explored.
The Institute of Medicine (2003)
www.ncbi.nlm.nih.gov/books/NB...
Concluded that people who received the 1976 swine influenza vaccine had an increased risk for developing GBS.
Exact reason for this association remains unknown.
Rotavirus vaccine Rotashield, (1999)
www.cdc.gov/vaccines/vpd-vac/...
The U.S. Advisory Committee on Immunization Practices (ACIP)
October 22, 1999 to no longer recommend use of the RotaShield® vaccine for infants,
because of an association between the vaccine and intussusception.
The results of the investigations showed that RotaShield® vaccine caused intussusception in some healthy infants
Within 2 weeks
Intussusception increased 20 to 30 times over the expected risk
(Less after the second and third dose)
CDC estimated that one or two additional cases of intussusception would be caused among each 10,000 infants vaccinated with RotaShield® vaccine.
Reanalysis of mRNA trial data
Dr. John Campbell
2.61M subscribers
Share
685,172 views Dec 30, 2022
Swine flu vaccine (1976), 1 serious event per 100,000 vaccinees, Vaccine withdrawn
Rotavirus vaccine Rotashield, (1999),1 to 2 serious events per 10,000 vaccinees, Vaccine withdrawn
Covid mRNA vaccines, 1 serious event per 800 vaccinees, Vaccine officially promoted
Serious adverse events of special interest following mRNA COVID-19 vaccination in randomized trials in adults
pubmed.ncbi.nlm.nih.gov/36055...
Free full text available
www.ncbi.nlm.nih.gov/pmc/arti...
Why We Question the Safety Profile of mRNA COVID-19 Vaccines
(Robert M Kaplan and Sander Greenland)
sensiblemed.substack.com/p/wh...
Using publicly available data from Pfizer and Moderna studies,
we found one serious adverse event for each 800 vaccinees.
That translates to about 1,250 serious events for each million vaccine recipients.
US, Spain, Australia
Study to evaluate serious adverse events of special interest observed in mRNA COVID-19 vaccine trials.
Secondary analysis of serious adverse events reported in the placebo-controlled, phase III randomized clinical trials,
of Pfizer and Moderna mRNA COVID-19 vaccines
Results
Pfizer and Moderna mRNA COVID-19 vaccines were associated with an excess risk of serious adverse events of special interest
Pfizer
10.1 per 10,000 vaccinated over placebo baselines of 17.6
Moderna
15.1 per 10,000 vaccinated over placebo baseline of 42.2
Combined, the mRNA vaccines
Associated with an excess risk of serious adverse events of special interest of 12.5 per 10,000 vaccinated
Pfizer trial
Pfizer vaccine group
52 serious AESI (27.7 per 10,000) were reported
Pfizer placebo group
33 serious AESI (17.6 per 10,000) were reported
36 % higher risk of serious adverse events in the vaccine group
Risk difference 18.0 per 10,000 vaccinated
Moderna trial
Moderna trial, vaccine group
87 serious AESI (57.3 per 10,000) were reported
Moderna trial, placebo group
64 serious AESI (42.2 per 10,000) were reported
6 % higher risk of serious adverse events in the vaccine group
Risk difference 7.1 per 10,000 vaccinated
Discussion
The excess risk of serious adverse events found in our study points to the need for formal harm-benefit analyses,
particularly those that are stratified according to risk of serious COVID-19 outcomes.
These analyses will require public release of participant level datasets.
Full transparency of the COVID-19 vaccine clinical trial data is needed,
to properly evaluate these questions.
Unfortunately, as we approach 2 years after release of COVID-19 vaccines,
participant level data remain inaccessible.
Level of adverse reactions in the past
The 1976 swine flu vaccine
Small increased risk of Guillain-Barré Syndrome
The increased risk was approximately 1 additional case of GBS for every 100,000 people who got the swine flu vaccine.
When over 40 million people were vaccinated against swine flu,
federal health officials decided that the possibility of an association of GBS with the vaccine, however small,
necessitated stopping immunization until the issue could be explored.
The Institute of Medicine (2003)
www.ncbi.nlm.nih.gov/books/NB...
Concluded that people who received the 1976 swine influenza vaccine had an increased risk for developing GBS.
Exact reason for this association remains unknown.
Rotavirus vaccine Rotashield, (1999)
www.cdc.gov/vaccines/vpd-vac/...
The U.S. Advisory Committee on Immunization Practices (ACIP)
October 22, 1999 to no longer recommend use of the RotaShield® vaccine for infants,
because of an association between the vaccine and intussusception.
The results of the investigations showed that RotaShield® vaccine caused intussusception in some healthy infants
Within 2 weeks
Intussusception increased 20 to 30 times over the expected risk
(Less after the second and third dose)
CDC estimated that one or two additional cases of intussusception would be caused among each 10,000 infants vaccinated with RotaShield® vaccine.