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To: exDemMom

“produce reams of safety and efficacy data in order to obtain FDA approval.”

Thanks for the laugh this evening.


36 posted on 07/06/2025 6:23:35 PM PDT by cgbg (It was not us. It was them--all along.)
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To: cgbg
For your reading pleasure, I have linked to the ClinicalTrials database. These are a couple of studies which I picked more or less at random, either in phase 3 (pre-approval) or phase 4 (FDA approved).

A Pragmatic Assessment of Influenza Vaccine Effectiveness in the DoD (PAIVED) This phase 4 study enrolled over 15,000 participants.

A Study to Evaluate a Modified RNA Vaccine Against Influenza in Adults 18 Years of Age or Older Over 30,000 participants completed this phase 3 study.

Each of these describes a single study. The typical drug approval process consists of conducting several studies at each phase of clinical trial.

If you want some bonus reading, go to the FDA website, choose a drug, and read all of the approval documents. There are usually several hundred pages of these.

I've yet to see any "alternative" practitioner publish a single study that even comes close to approaching the size, detail, and scope of the clinical studies required to obtain FDA approval.

40 posted on 07/09/2025 5:21:17 PM PDT by exDemMom (Dr. exDemMom, infectious disease and vaccines research specialist.)
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