Posted on 05/04/2021 2:18:13 PM PDT by ransomnote
Are people electing for the shot getting the opportunity to read the label?
I discussed the case of an individual who developed lower extremity blood clots shortly after the second dose of the Moderna vaccine today. Moderna RNA vaccine.
Cue the “oh yeah, right”, girl gif.
Step 0
Lack of long term testing
The mRNA vaccines have a known risk of ADE that the CDC, NIH, Fauci et. al. are hiding.
https://pubmed.ncbi.nlm.nih.gov/33113270/
It's impossible to tell. using laboratory assessments, if someone who has Covid-19 post vaccination got it through 'natural' infection because the 'vaccine' isn't 100% effective, or as a result of ADE from having the vaccination. Both develop antibodies.
A perspective on potential antibody-dependent enhancement of SARS-CoV-2 - PubMed (nih.gov)
Informed consent disclosure to vaccine trial subjects of risk of COVID-19 vaccines worsening clinical disease
Timothy Cardozo 1, Ronald Veazey 2
Affiliations expand
Free PMC article
Abstract
Aims of the study: Patient comprehension is a critical part of meeting medical ethics standards of informed consent in study designs. The aim of the study was to determine if sufficient literature exists to require clinicians to disclose the specific risk that COVID-19 vaccines could worsen disease upon exposure to challenge or circulating virus.
Methods used to conduct the study: Published literature was reviewed to identify preclinical and clinical evidence that COVID-19 vaccines could worsen disease upon exposure to challenge or circulating virus. Clinical trial protocols for COVID-19 vaccines were reviewed to determine if risks were properly disclosed.
Results of the study: COVID-19 vaccines designed to elicit neutralising antibodies may sensitise vaccine recipients to more severe disease than if they were not vaccinated. Vaccines for SARS, MERS and RSV have never been approved, and the data generated in the development and testing of these vaccines suggest a serious mechanistic concern: that vaccines designed empirically using the traditional approach (consisting of the unmodified or minimally modified coronavirus viral spike to elicit neutralising antibodies), be they composed of protein, viral vector, DNA or RNA and irrespective of delivery method, may worsen COVID-19 disease via antibody-dependent enhancement (ADE). This risk is sufficiently obscured in clinical trial protocols and consent forms for ongoing COVID-19 vaccine trials that adequate patient comprehension of this risk is unlikely to occur, obviating truly informed consent by subjects in these trials.
Conclusions drawn from the study and clinical implications: The specific and significant COVID-19 risk of ADE should have been and should be prominently and independently disclosed to research subjects currently in vaccine trials, as well as those being recruited for the trials and future patients after vaccine approval, in order to meet the medical ethics standard of patient comprehension for informed consent.
I'm guessing this happens so rarely that it would have been missed in long term trials of much smaller groups of people.
You almost have to unleash it on 100 million people to have enough cases to identify the blood clots as statistically significant.
My opinion.
J&J is the only shot of the 3 in the US that I would get, *if* I had to get a shot.
The obvious step 2 is to determine who is susceptible to this chain of events. Or did I miss something?
They still skipped long term testing and there have been a slew of side effects reported, many of which might have been caught.
https://media.tghn.org/medialibrary/2020/11/C4591001_Clinical_Protocol_Nov2020_Pfizer_BioNTech.pdf
Pfizer’s trial plan. Page 92 they talk about a 24 month follow up visit for people in the trial. I suppose that will happen in 2022.
1) you take this thoroughly UNTESTED vaccine
2) you get blood clots
Check out this article on the history of the drug Thalidomide:
https://en.wikipedia.org/wiki/Thalidomide
While it is not identical to the “rush to market” we have seen with these vaccines, there are some similarities.
Bottom line: Scientists didn’t really understand the drug until it caused a lot of damage, partially because it violated the belief at that time that drugs could not pass through the placental barrier.
Science is always learning—”statistically insignificant” may be in the eyes of the beholder.
This rare clotting issue occurs soon after vaccination. So for this situation, time isn’t an issue. Only sample size as you said.
Let’s say this clotting issue is unreported by a factor of 10. So in that case, the guestimate would be 1 in 100,000.
Estrogen-based birth control causes clotting in 1 out of 1,000. Just for perspective.
Do the research or you ARE the research.
Are people electing for the shot getting the opportunity to read the label?
= = =
If they can read English, and question the safety, they are White Supremacists.
And therefore deserve a triple vax dose..
A few years ago, I got a deep-vein thrombosis (big-league blood clot), which then caused a pulmonary embolism. As anyone who has had one of those knows — they’re not pleasant.
“When platelets are activated en masse, as can happen rarely after a person takes the blood thinner heparin....”
First I heard this — probably just as well that I didn’t know, when I was put on heparin. Heparin probably saved my life — but, it seems that it could have just ended it sooner.
BTW, heparin isn’t cheap, and it requires an injection. A daily injection, for six full months. The cure isn’t worse than the disease — but, it’s sure not a party drug.
BTW 2, a few days after a Pfizer shot, I got a very sore neck. It lasted about a week and a half, and just faded away. That was my only side-effect.
Yes lets just rush this crap onto people
Hell lets force them to take it
Don’t you mean the mRNA gene-therapy? According to Moderna that’s what is it, because that’s what the FDA considers mRNA treatments.
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