Sunday Feb 27, 2022
001 Blowing the whistle on the Pfizer mRNA trials with Brook Jackson
Brook Jackson was the former regional director for 2 of the 3 Ventavia clinical sites for the Pfizer mRNA trials. A few hours after her filing of a complaint with the FDA with regards to alleged fraud in the clinical sites she found herself being let go.
This episode we dive in to what happened during the trial that led to Brook blowing the whistle on the conduct of staff and management as well as her dismissal. We discuss the alleged fraud, administrative errors, issues with hard copy documents and electronic records not matching or being changed at the request of Pfizer directly, staff being so overwhelmed they were unable to follow up on adverse events - both serious and otherwise as well as her law suits filed against Ventavia & Pfizer and much much more!
Timeline
00:15 intro
02:02 CRO's/Ventavia/Pfizer
03:59 Small steps to blowing the whistle?
06:06 The issues with informed consent
10:45 Gaps in informed consent?
13:10 Staffing issues
20:20 Staffing issues with (serious) adverse event follow ups
23:40 Maddie De Garay
25:00 Missing info
31:30 Randomisation scheme in patient file
40:50 Ventavia was "only" 3 sites 1000 patients?
43:00 FDA didn't follow up.. fired hours after complaint!
48:00 Ventavia got more trials?
50:45 Why has it taken so long
51:30 Filing the lawsuits
1:01:05 Intimidation?
1:04:40 Text messages with Pfizer lawyer
1:12:00 Don't believe me, believe the evidence
1:16:00 document releases (18 Jan & end of Jan) don't add up to hard copy data
1:18:00
1:23:00 SAE is an AE? Fraud?
1:32:00 Phasing out/outro
Find her on
Referenced materials:
FDA Briefing document (page 42 for suspected covid cases)
https://www.fda.gov/media/144245/download
Article by EpochTimes where most of the lawsuit issues spoken about can be found
Maddie De Garay's mother on Tucker Carlson explaining her daughters case
https://www.foxnews.com/media/ohio-woman-daughter-covid-vaccine-reaction-wheelchair
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