Almost a year ago (their website states ‘Four
days
after the Pfizer vaccine was approved for ages 16+’, which was
on 23rd August 2021), PHMPT (which stands for Public Health and Medical Professionals for
Transparency) issued, through the law firm of Aaron
Siri and his partner, a request to the FDA pursuant
to the Freedom of
Information Act
(5 U.S.C. § 552, as amended) (“FOIA”) for “[a]ll
data and information for the Pfizer Vaccine enumerated in 21 C.F.R.
§ 601.51(e)5 with the exception of publicly available reports on the
Vaccine Adverse Events Reporting System”, which the FDA rejected
on 9th September 2021 on the basis that PHMT did “not
demonstrate[] a compelling need that involves an imminent threat to
the life or physical safety of an individual” or “that
there exists an urgency to inform the public concerning actual or
alleged Federal Government activity.” On 16th
September 2021, through their lawyer Aaron
Siri, PHMT went to court (Northern District of Texas, as PHMT is
based in Texas) ‘to challenge the FDA’s determination and
seeks an order compelling the FDA to produce responsive records on an expedited basis’ [page
3; my emphasis].
On 17th November, the FDA released the post-marketing experience report from section 5.3.6 of the BLA (biologics licence application) which Pfizer had submitted to the FDA (presumably on 30th April 2021, as this is the date displayed on the report). Two days later (web log: 19 November 2021, 16:13:39), PHMT published this very important document on their website, at https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf.
Note that after some dragging of the FDA’s feet, the same court in Texas (judge Mark Pittman, bravo!) ordered on 6th January 2022 the FDA to expedite the release of the documents ‘at a rate of 55,000 pages every 30 days, with the first production being due on or before March 1, 2022, until production is complete’. https://aaronsiri.substack.com/p/instead-of-fdas-requested-500-pages [My emphasis] This process is still on going.
Pfizer’s post-marketing report from section 5.3.6 of its biologics licence application is extremely important because it provides the number of adverse events (including deaths) recorded as at 28th February 2021, so for the 90 days or so since the roll-out of the vaccination campaign began in the USA and elsewhere (i.e. on 1st December 2020).
Although the number of vaccines distributed worldwide during that period was redacted [b) (4)], this was not the case for the numbers of adverse events (42,086) and deaths (1,223) brought to the attention of Pfizer (note that these figures are probably understated or under-reported by a factor of some 5x to 10x, as, for instance, in the USA doctors are NOT obliged by law to report adverse events to VAERS – the vaccine adverse event reporting system). One should also pay attention to the number of people who received the jab and who were not recovered (as at 28th February 2021): 11,361. Note also the number of people in the category ‘recovered’ but with sequelae: 520.
On 17th November, the FDA released the post-marketing experience report from section 5.3.6 of the BLA (biologics licence application) which Pfizer had submitted to the FDA (presumably on 30th April 2021, as this is the date displayed on the report). Two days later (web log: 19 November 2021, 16:13:39), PHMT published this very important document on their website, at https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf.
Note that after some dragging of the FDA’s feet, the same court in Texas (judge Mark Pittman, bravo!) ordered on 6th January 2022 the FDA to expedite the release of the documents ‘at a rate of 55,000 pages every 30 days, with the first production being due on or before March 1, 2022, until production is complete’. https://aaronsiri.substack.com/p/instead-of-fdas-requested-500-pages [My emphasis] This process is still on going.
Pfizer’s post-marketing report from section 5.3.6 of its biologics licence application is extremely important because it provides the number of adverse events (including deaths) recorded as at 28th February 2021, so for the 90 days or so since the roll-out of the vaccination campaign began in the USA and elsewhere (i.e. on 1st December 2020).
Although the number of vaccines distributed worldwide during that period was redacted [b) (4)], this was not the case for the numbers of adverse events (42,086) and deaths (1,223) brought to the attention of Pfizer (note that these figures are probably understated or under-reported by a factor of some 5x to 10x, as, for instance, in the USA doctors are NOT obliged by law to report adverse events to VAERS – the vaccine adverse event reporting system). One should also pay attention to the number of people who received the jab and who were not recovered (as at 28th February 2021): 11,361. Note also the number of people in the category ‘recovered’ but with sequelae: 520.
I suppose that if the media had done their job
and made this information known to the public as much as, say,
they like to demonise Russia or the anti-vaxxers, many lives could have been saved:
for the USA,
the UK, Australia and the EU, the data are 3,270,859 adverse
events and 62,450
deaths as at 28th June 2022
[information published on the website of the admirable
Australian Senator for Queensland Malcolm Roberts on 22nd
Aug. 2022: https://www.malcolmrobertsqld.com.au/barrister-releases-bombshell-legal-opinion-on-alleged-illegal-control-of-doctors-conduct/#_ftnref4].
Note that Naomi Wolf has assembled a team of volunteers who are examining the Pfizer document releases (as published on PHMT, I would suppose); their findings are being published on The Daily Clout, at https://dailyclout.io/category/campaigns/pfizer-documents-analysis.
Other links
https://phmpt.org/court-documents/
https://phmpt.org/wp-content/uploads/2021/11/091621-Complaint.pdf
https://phmpt.org/wp-content/uploads/2021/11/111521-Second-Joint-Status-Report.pdf
https://phmpt.org/pfizers-documents/
https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf
[Interview of Dr Daniel Nagase]
21:43
BC Doctor reviews 'shocking' stats from released Pfizer documents -(covid19 = flu)
SixthSense
First published at 12:57 UTC on 11th December 2021.
https://www.bitchute.com/video/BcnWB0VQ1B7l/
https://pandemictimeline.com/2021/12/the-fda-begins-dumping-documents-as-ordered/
https://expose-news.com/2021/12/06/pfizer-documents-reveal-both-pfizer-and-the-fda-knew-the-risks-of-vaccine-adverse-events-and-deaths/
https://expose-news.com/?s=Pfizer+document
7 Jan, 2022 05:29
Judge rules FDA can’t keep vaccine docs secret ‘until 2096’
A federal judge said the drug regulator must radically accelerate its release of hundreds of thousands of files on the Pfizer jab
https://www.rt.com/news/545350-fda-pfizer-vaccine-documents/
https://www.reuters.com/legal/government/paramount-importance-judge-orders-fda-hasten-release-pfizer-vaccine-docs-2022-01-07/
https://paulzanotelli.ch/blog/coronavirus/dissent/sasha-latypova/they-quickly-adjusted-their-dosage.html
https://paulzanotelli.ch/blog/coronavirus/dissent/steve-kirsch/this-vaccine-is-the-most-dangerous-vaccine-ever-created-by-man.html
https://paulzanotelli.ch/blog/coronavirus/dissent/david-knight/it-s-the-trump-shot.html
https://paulzanotelli.ch/blog/coronavirus/dissent/political/senator-ron-johnson/if-you-re-a-doctor.html
Note that Naomi Wolf has assembled a team of volunteers who are examining the Pfizer document releases (as published on PHMT, I would suppose); their findings are being published on The Daily Clout, at https://dailyclout.io/category/campaigns/pfizer-documents-analysis.
Other links
https://phmpt.org/court-documents/
https://phmpt.org/wp-content/uploads/2021/11/091621-Complaint.pdf
https://phmpt.org/wp-content/uploads/2021/11/111521-Second-Joint-Status-Report.pdf
https://phmpt.org/pfizers-documents/
https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf
[Interview of Dr Daniel Nagase]
21:43
BC Doctor reviews 'shocking' stats from released Pfizer documents -(covid19 = flu)
SixthSense
First published at 12:57 UTC on 11th December 2021.
https://www.bitchute.com/video/BcnWB0VQ1B7l/
https://pandemictimeline.com/2021/12/the-fda-begins-dumping-documents-as-ordered/
https://expose-news.com/2021/12/06/pfizer-documents-reveal-both-pfizer-and-the-fda-knew-the-risks-of-vaccine-adverse-events-and-deaths/
https://expose-news.com/?s=Pfizer+document
7 Jan, 2022 05:29
Judge rules FDA can’t keep vaccine docs secret ‘until 2096’
A federal judge said the drug regulator must radically accelerate its release of hundreds of thousands of files on the Pfizer jab
https://www.rt.com/news/545350-fda-pfizer-vaccine-documents/
https://www.reuters.com/legal/government/paramount-importance-judge-orders-fda-hasten-release-pfizer-vaccine-docs-2022-01-07/
https://paulzanotelli.ch/blog/coronavirus/dissent/sasha-latypova/they-quickly-adjusted-their-dosage.html
https://paulzanotelli.ch/blog/coronavirus/dissent/steve-kirsch/this-vaccine-is-the-most-dangerous-vaccine-ever-created-by-man.html
https://paulzanotelli.ch/blog/coronavirus/dissent/david-knight/it-s-the-trump-shot.html
https://paulzanotelli.ch/blog/coronavirus/dissent/political/senator-ron-johnson/if-you-re-a-doctor.html
Lausanne, the above was
published on the twenty-fifth day of
the eighth month of the year two
thousand and twenty-two.