No. It is an issue of you not understanding what constitutes a clinical trial. You could have said I took the vaccine under emergency authorization and had I experienced serious side effects necessitating medical care the data would have been collected. That would have been true.A) this isn't about the detail of working knowledge of a clinical trial
B) you're still refusing to understand you are in the effective trial now as the EUA mandates for the release of the injections.
C) I've shared what was told to me by legitimately credentialed/experienced folks ... they disagree with your assessment of clinical trial, evidently, and recognize the real trial started just over a year ago ... in both time and NUMBERs of participants.
But you are mistaken when you equate emergency authorizations to clinical trials. Placebos are not a component with emergency authorization, there is no control group in a study, the pharmaceutical company does not maintain data on individuals receiving shots under emergency authorization.
You simply got confused, missing up emergency authorization with clinical trials. Maybe you've been reading too much propaganda to keep things straight?