Why would a medical professional who was responsible for injecting an individual with an mRNA injection which caused death report it through the system? When VAers reports 47.000 deaths which is probably less than 5% of total deaths actually occurring over the last 4 years not cause our medical leadership to demand an immediate moratorium on all injections until they are proven to be safe and actually have a positive treatment outcome over cheap repurposed drugs. That is the study NIH should demand.
The existing data was available in CSV files. However, they split the columns of the database into 3 separate files. But you can't easily merge them back together into one spreadsheet because the rows don't line up. In one CSV file a patient report may take up 1 row but in the corresponding CSV file the same patient report takes up 3 rows. So to even do basic column filters using excel you need a sophisticated statistical analysis software code to match up all of the rows to get one patient report per row. I assume that this was being done on purpose.
In the ‘90s Barbara Lowe Fisher had a conference in Washington DC. A statistician who wrote books used in colleges worked for 3 years with his Representative to gain access to VAERS.
His daughter had reacted to the Hep B injection at birth (Dr insisted it wasn’t the vaccine!) She died in the drs office when given the Hep B at two months.
His closing statement about the VAERS statistics: “If any major corporation manipulated their statistics the way they do at VAERS, all of the officials would be in prison.”
He didn’t blame it on old outdated computers; he said deliberate manipulation of the statics.
I’m glad we have different people in charge of the data.
Barbara Loe Fisher, from the NVIC? She did a somewhat recent, in-depth interview, detailing the 1986 Childhood Vaccine Injury Act. She was told, it was going through, no matter what and she did what she could to try to warn people and still does! So sad so many millions of Americans, have no idea... https://www.nvic.org/about/history
Dr Malone: in a short time the FDA is going to pull the natural thyroid meds from the market. This was determined before the current administration. The only reason is so Big Pharma gets all the business. Many thousands of people depend on natural thyroid because they cannot tolerate the synthetic T4 drugs and that will be it for us. I don't know if Makary is even aware of all this and the nightmare that is about to hit so many. Can you bring this to his attention? We just want to be allowed to keep taking what has saved us
I can understand your hesitancy around the actual outcomes promised. These departments are quick to make statements of change for the better, while not implementing them satisfactorily. Thomas has an excellent point about the incentives to report. There aren't many for the average doctor or healthcare provider. We'll see is so appropriate.
Makes one a bit dizzy. Good show though. Will be watching for reports from those early users.
As an every man/woman it may be further useful for us to⁹ learn about supplements.
Depending on ease of use, it could be very helpful fir lawyers in deciding whether to take cases, as well as developing evidence. It will be interesting to see how the courts regard it.
Another interesting aspect will be whether it will be useful for practicing physicians - as a supplement to their computerized practice guidance. Maybe for new therapeutics and informed consent purposes?
Surely congratulations to Trump, Kennedy, HHS and the computer engineers! Fingers crossed its a full scale success.
Is the point to make the adverse event data useable? I am not aware that the old systems’ data were incorporated into drug safety analyses, is that correct?
The problem is that an application that could be produced by 5 DBAs, 2 programmers, and 2 UI designers with one coordinator in 3 months will be created by 10 health administrators, 20 assistants and a barista in 5 months, reviewed by congressional committee for a month, another 3 months to adjust for suggestions and objections submitted by our technically literate representatives (can we require an IQ test?), back for review of a month, final product 2 months later. The result is the horse designed by a committee -- a camel. And it will be produced in the newest database interface language spoken by a total of 12 people who all reside in India. I really can't wait.
My last similar project was 3 DBAs, 2 programmers, 2 data importer/translate people and plenty of hardware and support folks. All very good. Supervised by 2 government attorneys (???). The teckies had a workable system in a couple months, not complete but adequate. Attorneys said can you add a couple things? Sure, in the next release. No, gotta be now or no approval. 3 months later, same routine, exactly. A year later, I'd left for another project but called a friend from the group and he said the scope creep continued.
Why would a medical professional who was responsible for injecting an individual with an mRNA injection which caused death report it through the system? When VAers reports 47.000 deaths which is probably less than 5% of total deaths actually occurring over the last 4 years not cause our medical leadership to demand an immediate moratorium on all injections until they are proven to be safe and actually have a positive treatment outcome over cheap repurposed drugs. That is the study NIH should demand.
Transparency always does and always will depend on who’s controlling the information.
The existing data was available in CSV files. However, they split the columns of the database into 3 separate files. But you can't easily merge them back together into one spreadsheet because the rows don't line up. In one CSV file a patient report may take up 1 row but in the corresponding CSV file the same patient report takes up 3 rows. So to even do basic column filters using excel you need a sophisticated statistical analysis software code to match up all of the rows to get one patient report per row. I assume that this was being done on purpose.
In the ‘90s Barbara Lowe Fisher had a conference in Washington DC. A statistician who wrote books used in colleges worked for 3 years with his Representative to gain access to VAERS.
His daughter had reacted to the Hep B injection at birth (Dr insisted it wasn’t the vaccine!) She died in the drs office when given the Hep B at two months.
His closing statement about the VAERS statistics: “If any major corporation manipulated their statistics the way they do at VAERS, all of the officials would be in prison.”
He didn’t blame it on old outdated computers; he said deliberate manipulation of the statics.
I’m glad we have different people in charge of the data.
Barbara Loe Fisher, from the NVIC? She did a somewhat recent, in-depth interview, detailing the 1986 Childhood Vaccine Injury Act. She was told, it was going through, no matter what and she did what she could to try to warn people and still does! So sad so many millions of Americans, have no idea... https://www.nvic.org/about/history
Thanks for posting Docs.
Trust and verify. I’ll suspend comment until I hear from my favorite Safety Signal Sleuthing Surfer - Dr. Jessica Rose.
One small step for an agency; one great leap for transparency (hopefully).
Dr Malone: in a short time the FDA is going to pull the natural thyroid meds from the market. This was determined before the current administration. The only reason is so Big Pharma gets all the business. Many thousands of people depend on natural thyroid because they cannot tolerate the synthetic T4 drugs and that will be it for us. I don't know if Makary is even aware of all this and the nightmare that is about to hit so many. Can you bring this to his attention? We just want to be allowed to keep taking what has saved us
I can understand your hesitancy around the actual outcomes promised. These departments are quick to make statements of change for the better, while not implementing them satisfactorily. Thomas has an excellent point about the incentives to report. There aren't many for the average doctor or healthcare provider. We'll see is so appropriate.
Makes one a bit dizzy. Good show though. Will be watching for reports from those early users.
As an every man/woman it may be further useful for us to⁹ learn about supplements.
Depending on ease of use, it could be very helpful fir lawyers in deciding whether to take cases, as well as developing evidence. It will be interesting to see how the courts regard it.
Another interesting aspect will be whether it will be useful for practicing physicians - as a supplement to their computerized practice guidance. Maybe for new therapeutics and informed consent purposes?
Surely congratulations to Trump, Kennedy, HHS and the computer engineers! Fingers crossed its a full scale success.
Thanks so much for sharing!
Is the point to make the adverse event data useable? I am not aware that the old systems’ data were incorporated into drug safety analyses, is that correct?
The problem is that an application that could be produced by 5 DBAs, 2 programmers, and 2 UI designers with one coordinator in 3 months will be created by 10 health administrators, 20 assistants and a barista in 5 months, reviewed by congressional committee for a month, another 3 months to adjust for suggestions and objections submitted by our technically literate representatives (can we require an IQ test?), back for review of a month, final product 2 months later. The result is the horse designed by a committee -- a camel. And it will be produced in the newest database interface language spoken by a total of 12 people who all reside in India. I really can't wait.
My last similar project was 3 DBAs, 2 programmers, 2 data importer/translate people and plenty of hardware and support folks. All very good. Supervised by 2 government attorneys (???). The teckies had a workable system in a couple months, not complete but adequate. Attorneys said can you add a couple things? Sure, in the next release. No, gotta be now or no approval. 3 months later, same routine, exactly. A year later, I'd left for another project but called a friend from the group and he said the scope creep continued.
I cannot wait until @Datarepublican, gets their hands on this data base!!
Are they still lying about the DMED database?
More data manipulation to “merge” the files, hmmm—the only thing radically transparent is impudence in lying.