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Tim Price 😃's avatar

Kudos for standing up to what is clearly both a grotesque false narrative and a crime against humanity.

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SQ's avatar

Whenever "safety" is mentioned, I ask "What type of safety data are you referring to?"

In clinical trials, safety data is comprised of lab results, procedural results, and adverse event reporting. In normal phase 2/3 studies, lab work is done prior to being given the drug and afterwards, at at many visits throughout the trial. There are also procedures like ECGs, vitals, physical exams, etc. For a simple asthma medication, we would do serial labs where we would do ECG, vitals, lots of labs, then dose the patient, then repeat all the procedures at 1 hr post dose, 4 hrs post, etc. We would do this at multiple visits. For some reason, vaccines do not follow this standard. But these mRNAs were "first in class" and should have undergone all the previously mentioned tests.

If you read the Pfizer protocol, their combined phase 2/3 only tested for immunogenicity. That was it. No other labs or ECGs or even vitals were done. How can they possibly claim "safety" when they did no tests?

The only "safety" data they used were adverse events reported during the trial and then proceeded to ignore AE reporting systems like VAERs.

It is unbelievable that no pre/post drug labs or procedures were done. They have no idea (or they do) what happens in the body after injection.

So, ask them: When you say safety data, what data are you referring to? What tests were done to show safety? Were there changes in ECGs pre and post dose? How about liver function? Cardiac enzymes? Inflammatory biomarkers? Heart rate? Blood pressure?

They know nothing.

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