by Den 16 september 2021 stämde PUBLIC HEALTH AND MEDICAL PROFESSIONALS FOR TRANSPARENCY”, FDA – FOOD AND DRUG ADMINISTRATION, för att de vägrade/krävde 75 år för att lämna ut de dokument, som Pfizer hade lämnat in, för att få Comirnaty godkänt.
Ansökan fick bifall och den 6 januari beordrade UNITED STATES DISTRICT COURT FOR THE NORTHERN DISTRICT OF TEXAS FORT WORTH DIVISION, FDA att lämna ut dokumenten under 8 månader, det vill säga betydligt fortare än 75 år.
”The Food and Drug Administration won’t have 75 years to release thousands of pages of documents it relied on to license its COVID-19 vaccine. Instead, the federal agency will have just over eight months to do so, per a federal judge’s ruling.
The timeline ordered Thursday by U.S. District Judge Mark Pittman radically shortens the timeline under which the FDA has to produce troves of documents. The order stems from a Freedom of Information Act document lawsuit by a coalition of doctors and scientists with the nonprofit Public Health and Medical Professionals for Transparency. The group seeks an estimated 450,000 pages of material about the vaccine-creation process during the COVID-19 pandemic, which came into full force in the United States in March 2020.”
”Public Health and Medical Professionals for Transparency said the data should be made public quickly because the FDA took just under four months to review the data before granting full approval for the Pfizer-BioNTech COVID-19 vaccine.”
Av studien, som omfattade [TYVÄRR CENSURERAT AV FDA] personer under tre månader, drabbades 42 086 personer av 158 893 medicinska händelser/biverkningar.
Av dessa, avled 1 223 personer. 19 582 återhämtade sig. 520 återhämtade sig med följdsjukdomar. 11 361 hade inte återhämtat sig när rapporten skrevs.
”It is estimated that approximately [TYVÄRR CENSURERAT AV FDA] doses of BNT162b2 were shipped worldwide from the receipt of the first temporary authorisation for emergency supply on 01 December 2020 through 28 February 2021.
Cumulatively, through 28 February 2021, there was a total of 42,086 case reports (25,379 medically confirmed and 16,707 non-medically confirmed) containing 158,893 events. Most cases (34,762) were received from United States (13,739), United Kingdom (13,404) Italy (2,578), Germany (1913), France (1506), Portugal (866) and Spain (756); the remaining 7,324 were distributed among 56 other countries.”
Ännu vet ingen förutom Pfizer och FDA hur många personer som studien om tre månader omfattade.
Det första som sticker ut, är att de allvarliga biverkningarna utgör en stor del av alla inrapporterade biverkningar.
Hursomhelst, blir det intressant att de del av de resterande dokumenten och förhoppningsvis även antalet ”deltagare”.
Källa:
https://phmpt.org/pfizers-documents/
Observera särskilt detta dokument, https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf, på sidan 8, som bilden till artikeln kommer ifrån.
