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001 Blowing the whistle on the Pfizer mRNA trials with Brook Jackson

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Innehåll tillhandahållet av Sunny S. Allt poddinnehåll inklusive avsnitt, grafik och podcastbeskrivningar laddas upp och tillhandahålls direkt av Sunny S eller deras podcastplattformspartner. Om du tror att någon använder ditt upphovsrättsskyddade verk utan din tillåtelse kan du följa processen som beskrivs här https://sv.player.fm/legal.

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

www.iambrookjackson.com

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

https://www.theepochtimes.com/exclusive-pfizer-trial-whistleblower-presses-forward-with-lawsuit-without-us-governments-help_4277153.html?utm_source=partners&utm_campaign=allen

Maddie De Garay's mother on Tucker Carlson explaining her daughters case

https://www.foxnews.com/media/ohio-woman-daughter-covid-vaccine-reaction-wheelchair

  continue reading

29 episoder

Artwork
iconDela
 
Manage episode 321438466 series 3321339
Innehåll tillhandahållet av Sunny S. Allt poddinnehåll inklusive avsnitt, grafik och podcastbeskrivningar laddas upp och tillhandahålls direkt av Sunny S eller deras podcastplattformspartner. Om du tror att någon använder ditt upphovsrättsskyddade verk utan din tillåtelse kan du följa processen som beskrivs här https://sv.player.fm/legal.

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

www.iambrookjackson.com

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

https://www.theepochtimes.com/exclusive-pfizer-trial-whistleblower-presses-forward-with-lawsuit-without-us-governments-help_4277153.html?utm_source=partners&utm_campaign=allen

Maddie De Garay's mother on Tucker Carlson explaining her daughters case

https://www.foxnews.com/media/ohio-woman-daughter-covid-vaccine-reaction-wheelchair

  continue reading

29 episoder

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