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To: ransomnote
Meanwhile, the US CDC and FDA have lifted their recommended pause on use of Johnson & Johnson’s coronavirus vaccine with a condition that it will now include a safety label warning that its vaccine comes with blood clot risks.

Are people electing for the shot getting the opportunity to read the label?

2 posted on 05/04/2021 2:23:29 PM PDT by frogjerk (I will not do business with fascists)
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To: frogjerk
Are people electing for the shot getting the opportunity to read the label?

 

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 1Ronald 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.

6 posted on 05/04/2021 2:35:18 PM PDT by ransomnote (IN GOD WE TRUST)
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To: frogjerk

J&J is the only shot of the 3 in the US that I would get, *if* I had to get a shot.


8 posted on 05/04/2021 2:50:22 PM PDT by for-q-clinton (Cancel Culture IS fascism...Let's start calling it that!)
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To: frogjerk

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..


16 posted on 05/04/2021 3:51:14 PM PDT by Scrambler Bob
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