{"id":210864,"date":"2021-12-01T19:00:00","date_gmt":"2021-12-02T00:00:00","guid":{"rendered":"https:\/\/z3news.com\/w\/?p=210864"},"modified":"2021-12-02T15:17:05","modified_gmt":"2021-12-02T20:17:05","slug":"fda-wants-55-years-to-release-covid-jab-reaction-data","status":"publish","type":"post","link":"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/","title":{"rendered":"FDA Wants 55 Years to Release COVID Jab Reaction Data"},"content":{"rendered":"<hr \/>\n<h3 id=\"expanderHead\" data-jsid=\"expanderHead\">STORY AT-A-GLANCE<\/h3>\n<div id=\"expanderContent\" data-jsid=\"expanderContent\">\n<ul>\n<li><span id=\"bcr_rptStory_cslStory_0\">In September 2021, a group called Public Health and Medical Professionals for Transparency (PHMPT) filed a Freedom of Information Act (FOIA) request with the FDA to obtain the documentation used to approve Comirnaty. When, after a month, the FDA had not replied, the PHMPT sued<\/span><\/li>\n<li><span id=\"bcr_rptStory_cslStory_1\">It took the U.S. Food and Drug Administration 108 days to \u201cthoroughly and completely\u201d review the 329,000 pages of data Pfizer\/BioNTech submitted to gain FDA approval for its Comirnaty COVID shot, which was licensed August 3, 2021<\/span><\/li>\n<li><span id=\"bcr_rptStory_cslStory_2\">The FDA now claims it needs 55 years to release those same pages to the public (at a rate of 500 pages per month), as each page must be reviewed and sensitive information redacted<\/span><\/li>\n<li><span id=\"bcr_rptStory_cslStory_3\">The FDA has so far only released 91 pages. These documents show that within the first 2.5 months of the Pfizer shot\u2019s rollout, Pfizer received 42,086 reports of adverse events, including 1,223 fatalities<\/span><\/li>\n<li><span id=\"bcr_rptStory_cslStory_4\">While Pfizer admits it received such a large number of spontaneous adverse event reports that they had to hire a redacted number of additional full-time personnel to handle the additional data entry, they claim that \u201cThe findings of these signal detection analyses are consistent with the known safety profile of the vaccine.\u201d If they expected this volume of injuries, why were they short-staffed \u2014 and why does the FDA think the number of new hires is proprietary information?<\/span><\/li>\n<\/ul>\n<\/div>\n<p>It took the U.S. Food and Drug Administration 108 days to review all the data Pfizer\/BioNTech submitted in order to gain FDA approval for its Comirnaty COVID shot, which was licensed August 3, 2021.<\/p>\n<p>Considering the agency claims there are 329,000 pages of data, the fact that they were able to read, analyze and draw conclusions about its safety and effectiveness in just 108 days \u2014 about 80,000 pages a month \u2014 is no small miracle. They must employ some very efficient speed readers.<\/p>\n<p>And that is why the FDA\u2019s claim that it now needs over half a century to review the documents before they can release them to the public doesn\u2019t seem very credible. Even Reuters has expressed shock, and its former CEO is on the board of Pfizer.<sup style=\"font-size: 10px;\"><span id=\"edn1\" data-hash=\"#ednref1\">1<\/span><\/sup><\/p>\n<h2>Expedited FOIA Request for Comirnaty Data<\/h2>\n<p>In September 2021, a group called Public Health and Medical Professionals for Transparency (PHMPT) filed a Freedom of Information Act (FOIA) request with the FDA to obtain the documentation used to approve Comirnaty.<\/p>\n<p>This includes safety and effectiveness data, adverse reaction reports and lists of active and inactive ingredients. Approximately 400 additional FOIA requests by other individuals for all or part of this information have also been filed.<sup style=\"font-size: 10px;\"><span id=\"edn2\" data-hash=\"#ednref2\">2<\/span><\/sup><\/p>\n<p>In their FOIA application, the PHMPT asked the agency to expedite release of the documents \u2014 a reasonable request, considering we have no raw data and the shots are being pushed on children as young as 5.<\/p>\n<p>FOIA guidelines include two conditions upon which a request may be expedited. One is \u201cif the lack of expedited treatment could reasonably be expected to pose a threat to someone\u2019s life or physical safety,\u201d which one could easily argue is the case here.<\/p>\n<p>The second condition is \u201cif there is an urgency to inform the public about an actual or alleged federal government activity, if made by a person who is primarily engaged in disseminating information.\u201d This too is clearly applicable.<\/p>\n<blockquote><p><em>\u201cDuring a time when COVID-19 vaccine mandates are being implemented over the objection of those that have questions about the data and information supporting the safety and efficacy of the Pfizer Vaccine, and individuals with these questions are being expelled from employment, school, transportation, and the military, the public has an urgent and immediate need to have access to this data,\u201d<\/em> the PHMPT said in its request.<sup style=\"font-size: 10px;\"><span id=\"edn3\" data-hash=\"#ednref3\">3<\/span><\/sup><\/p><\/blockquote>\n<h2>FDA Now Wants 55 Years to Release COVID Jab Data<\/h2>\n<p>When, after a month, the FDA still had not responded to the FOIA request, the PHMPT sued.<sup style=\"font-size: 10px;\"><span id=\"edn4\" data-hash=\"#ednref4\">4<\/span><\/sup> The FDA is now asking a federal judge to allow them to delay the full release of all documents until 2076 \u2014 55 years from now.<\/p>\n<p>According to the U.S. Department of Justice (DOJ) attorney who represents the FDA in this case, the agency will be able to \u201cprovide more pages to more requesters\u201d if allowed to stick to a rolling schedule of 500 pages per month, \u201cthus avoiding a system where a few large requests monopolize finite processing resources.\u201d<\/p>\n<p>They claim they only have 10 employees assigned to FOIA releases, and before material can be released, an FDA official has to go through them and redact any information that might reveal personal information about clinical trial participants and any confidential business or trade secret information.<\/p>\n<p>The 1967 FOIA law requires federal agencies to respond to FOIAs within 20 days unless \u201cunusual circumstances\u201d exist that prevent a timely release. Circumstances that might warrant an extended release schedule include:<\/p>\n<ul>\n<li>Instances where response records must be searched for and collected from an entity other than the office processing the request<\/li>\n<li>Situations involving \u201cvoluminous\u201d amounts of records that must be compiled, and<\/li>\n<li>Instances requiring consultation with another federal agency that has a substantial interest in the information<\/li>\n<\/ul>\n<p>The DOJ attorney points out that the court has allowed for a 500-page maximum per month release schedule in other cases, and should allow the FDA the same leeway here.<\/p>\n<aside class=\"takeaway tamiddle\">While it can conduct that intense review of Pfizer\u2019s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public. ~ Aaron Siri, attorney for PHPMT<\/aside>\n<p>Plaintiffs, on the other hand, argue the agency should be able to release everything by early March 2022, noting the FDA employs 18,000 people and has an annual budget of $6 billion. Between 2008 and 2017, the agency processed 114,938 FOIA requests, of which it granted 72.4%, either fully or partially.<\/p>\n<p>Of those, 39.8% were designated as \u201ccomplex,\u201d and 81.5% of these complex FOIA requests were granted in 61 days or more. Considering these historical statistics, a backlog of 400 FOIA requests doesn\u2019t appear excessively burdensome.<\/p>\n<h2>FDA\u2019s Foot-Dragging Is Suspicious<\/h2>\n<p>Then there\u2019s the sticky issue that it has already proven its capacity for rapid review. Aaron Siri of the law firm Siri &amp; Glimstad wrote in the PHMPT\u2019s court filing:<sup style=\"font-size: 10px;\"><span id=\"edn5\" data-hash=\"#ednref5\">5<\/span>,<\/sup><sup style=\"font-size: 10px;\"><span id=\"edn6\" data-hash=\"#ednref6\">6<\/span>,<\/sup><sup style=\"font-size: 10px;\"><span id=\"edn7\" data-hash=\"#ednref7\">7<\/span>,<\/sup><sup style=\"font-size: 10px;\"><span id=\"edn8\" data-hash=\"#ednref8\">8<\/span><\/sup><\/p>\n<blockquote><p><em>\u201cThis 108-day period is the same amount of time it took the FDA to review the responsive documents for the far more intricate task of licensing Pfizer&#8217;s COVID-19 vaccine &#8230;<\/em><\/p><\/blockquote>\n<blockquote><p><em>It took the FDA precisely 108 days from when Pfizer started producing the records for licensure to when the FDA licensed the Pfizer vaccine. Taking the FDA at its word, it conducted an intense, robust, thorough, and complete review and analysis of those documents in order to assure that the Pfizer vaccine was safe and effective for licensure.<\/em><\/p><\/blockquote>\n<blockquote><p><em>While it can conduct that intense review of Pfizer\u2019s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public &#8230;<\/em><\/p><\/blockquote>\n<blockquote><p><em>The entire purpose of the FOIA is to assure government transparency. It is difficult to imagine a greater need for transparency than immediate disclosure of the documents relied upon by the FDA to license a product that is now being mandated to over 100 million Americans under penalty of losing their careers, their income, their military service status, and far worse.\u201d<\/em><\/p><\/blockquote>\n<h2>Shocking Revelations in First Batch of FOIA Docs<\/h2>\n<p>Two months after the lawsuit against it was filed, the FDA released a batch of 91 pages,<sup style=\"font-size: 10px;\"><span id=\"edn9\" data-hash=\"#ednref9\">9<\/span><\/sup> and if this batch is any indication, it\u2019s not surprising that the FDA wants to slow-walk the release of the rest. In a November 21, 2021, substack article, Kyle Becker cites directly from the released documents:<sup style=\"font-size: 10px;\"><span id=\"edn10\" data-hash=\"#ednref10\">10<\/span><\/sup><\/p>\n<blockquote><p><em>\u201c\u2019It is estimated that approximately [REDACTED] doses of BNT162b2 were shipped worldwide from the receipt of the first temporary authorization for emergency supply on 01 December 2020 through 28 February 2021,\u2019 the document states. \u2018Cumulatively, 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 &#8230;<\/em><\/p><\/blockquote>\n<blockquote><p><em>Most cases (34,762) were received from United States (13,739), United Kingdom (13,404) Italy (2,578), Germany (1913), France (1506), Portugal (866).\u2019 Below is a General Overview of the reported outcomes to the Adverse Events:<\/em><\/p><\/blockquote>\n<div class=\"center-img\"><img decoding=\"async\" style=\"width: 100%; max-width: 600px !important;\" src=\"https:\/\/media.mercola.com\/ImageServer\/public\/2021\/November\/general-overview-of-the-reported-outcomes-to-the-adverse-events.jpg\" alt=\"reported outcomes to the adverse events\" \/><\/div>\n<blockquote><p><em>The chart lists 1,223 fatal outcomes in the Relevant Cases. Interestingly, the age range with the most relevant cases was 31-50 years old, which is not the age group considered to be at high risk from COVID-19.\u201d<\/em><\/p><\/blockquote>\n<p>It\u2019s worth noting that by redacting the specified number of doses shipped, it becomes more difficult to assess the potential ratio of injury. Still, even without that, 42,086 reports of injury, including 1,223 fatalities, are a significant signal in and of itself, especially when you consider that the 1976 swine flu vaccine was pulled after 25 deaths.<\/p>\n<h2>Glaring Disregard for Life<\/h2>\n<p>It\u2019s even more disturbing when you consider that those 42,086 reports were received by Pfizer in just the first 2.5 months of the shot being rolled out. Pfizer even acknowledges the abnormal rate of injuries, but then sweeps it aside as being of no consequence. As noted by Siri, in a November 19, 2021 substack article, in which he discusses this first batch of documents:<sup style=\"font-size: 10px;\"><span id=\"edn11\" data-hash=\"#ednref11\">11<\/span><\/sup><\/p>\n<blockquote><p><em>\u201cPfizer explains, on page 6, that \u2018Due to the large numbers of spontaneous adverse event reports received for the product, [Pfizer] has prioritized the processing of serious cases\u2026\u2019<\/em><\/p><\/blockquote>\n<blockquote><p><em>Pfizer \u2018has also taken a [sic] multiple actions to help alleviate the large increase of adverse event reports\u2019 including \u2018increasing the number of data entry and case processing colleagues\u2019 and \u2018has onboarded approximately [REDACTED] additional fulltime employees (FTEs).\u2019<\/em><\/p><\/blockquote>\n<blockquote><p><em>Query why it is proprietary to share how many people Pfizer had to hire to track all of the adverse events being reported shortly after launching its product &#8230;<\/em><\/p><\/blockquote>\n<blockquote><p><em>But no cause for alarm since Pfizer explains to the FDA: \u2018The findings of these signal detection analyses are consistent with the known safety profile of the vaccine.\u2019 So, if they knew these issues were going to arise, then why didn\u2019t they appear to have enough staff to process this expected volume of reports?<\/em><\/p><\/blockquote>\n<blockquote><p><em>The grand conclusion by Pfizer to the FDA: \u2018The data do not reveal any novel safety concerns or risks requiring label changes and support a favorable benefit risk profile of to the BNT162b2 vaccine.\u2019 Nothing to see here.\u201d<\/em><\/p><\/blockquote>\n<p>Clearly, there\u2019s plenty to be seen in the hundreds of thousands of documents Pfizer\/BioNTech submitted to the FDA. The fact that the FDA is stonewalling and wants 55 years to redact them before they\u2019re fit for public view is telling in and of itself.<\/p>\n<p>You don\u2019t need a fanciful imagination to comprehend what they might be hiding. It almost seems they want to make sure the responsible parties are all dead by the time the full data set is out in the open and people can be held to account for their decisions. Let\u2019s hope the judge is more interested in public health than protecting the FDA\u2019s dirty secrets.<\/p>\n<h2 id=\"heading\" class=\"title link16\" data-jsid=\"sourcesReferencesBtn\">Sources and References<\/h2>\n<div id=\"contentrefsources\" class=\"contentrefsources\" data-jsid=\"sourcesReferences\">\n<div id=\"bcr_divReferences\" class=\"references\">\n<ul id=\"footnote-references2\">\n<li><sup><span id=\"ednref1\" data-hash=\"#edn1\"><span id=\"lblReferenceNo\">1<\/span><\/span><\/sup>\u00a0<a id=\"lnkReference\" href=\"https:\/\/www.zerohedge.com\/markets\/wait-what-even-reuters-tripping-out-55-year-delay-release-pfizer-vax-data\" target=\"_blank\" rel=\"noopener nofollow\">ZeroHedge November 23, 2021<\/a><\/li>\n<li><sup><span id=\"ednref2\" data-hash=\"#edn2\"><span id=\"lblReferenceNo\">2,<\/span><\/span><\/sup>\u00a0<sup><span id=\"ednref7\" data-hash=\"#edn7\"><span id=\"lblReferenceNo\">7<\/span><\/span><\/sup>\u00a0<a id=\"lnkReference\" href=\"https:\/\/www.dailymail.co.uk\/health\/article-10222035\/FDA-says-need-55-YEARS-make-vaccine-related-information-available-public.html\" target=\"_blank\" rel=\"noopener nofollow\">Daily Mail November 19, 2021, Updated November 20, 2021<\/a><\/li>\n<li><sup><span id=\"ednref3\" data-hash=\"#edn3\"><span id=\"lblReferenceNo\">3,<\/span><\/span><\/sup>\u00a0<sup><span id=\"ednref4\" data-hash=\"#edn4\"><span id=\"lblReferenceNo\">4<\/span><\/span><\/sup>\u00a0<a id=\"lnkReference\" href=\"https:\/\/childrenshealthdefense.org\/defender\/fda-licensing-pfizer-comirnaty-covid-vaccine\/\" target=\"_blank\" rel=\"noopener nofollow\">The Defender November 19, 2021<\/a><\/li>\n<li><sup><span id=\"ednref5\" data-hash=\"#edn5\"><span id=\"lblReferenceNo\">5<\/span><\/span><\/sup>\u00a0<a id=\"lnkReference\" href=\"https:\/\/fingfx.thomsonreuters.com\/gfx\/legaldocs\/klvykdlryvg\/vaccine%20foia%20complaint.pdf\" target=\"_blank\" rel=\"noopener nofollow\">US District Court Northern District of Texas Case 4:21-cv-01058-P<\/a><\/li>\n<li><sup><span id=\"ednref6\" data-hash=\"#edn6\"><span id=\"lblReferenceNo\">6<\/span><\/span><\/sup>\u00a0<a id=\"lnkReference\" href=\"https:\/\/www.sirillp.com\/wp-content\/uploads\/2021\/11\/020-Second-Joint-Status-Report-8989f1fed17e2d919391d8df1978006e.pdf\" target=\"_blank\" rel=\"noopener nofollow\">US District Court Northern District of Texas Case 4:21-cv-01058-P Second Joint Report<\/a><\/li>\n<li><sup><span id=\"ednref8\" data-hash=\"#edn8\"><span id=\"lblReferenceNo\">8<\/span><\/span><\/sup>\u00a0<a id=\"lnkReference\" href=\"https:\/\/thevaccinereaction.org\/2021\/11\/fda-asks-court-for-55-years-to-fully-release-documents-on-pfizer-covid-biologic\/\" target=\"_blank\" rel=\"noopener nofollow\">The Vaccine Reaction November 21, 2021<\/a><\/li>\n<li><sup><span id=\"ednref9\" data-hash=\"#edn9\"><span id=\"lblReferenceNo\">9<\/span><\/span><\/sup>\u00a0<a id=\"lnkReference\" href=\"https:\/\/phmpt.org\/pfizers-documents\/\" target=\"_blank\" rel=\"noopener nofollow\">PHMPT.org Pfizer documents<\/a><\/li>\n<li><sup><span id=\"ednref10\" data-hash=\"#edn10\"><span id=\"lblReferenceNo\">10<\/span><\/span><\/sup>\u00a0<a id=\"lnkReference\" href=\"https:\/\/thekylebecker.substack.com\/p\/the-fda-produced-first-batch-of-confidential\" target=\"_blank\" rel=\"noopener nofollow\">thekylebecker.substack.com November 21, 2021<\/a><\/li>\n<li><sup><span id=\"ednref11\" data-hash=\"#edn11\"><span id=\"lblReferenceNo\">11<\/span><\/span><\/sup>\u00a0<a id=\"lnkReference\" href=\"https:\/\/aaronsiri.substack.com\/p\/fda-produces-the-first-91-pages-of\" target=\"_blank\" rel=\"noopener nofollow\">aaronsiri.substack.com November 19, 2021<\/a><\/li>\n<\/ul>\n<hr \/>\n<p><em>Originally published by\u00a0<a href=\"http:\/\/articles.mercola.com\/sites\/articles\/archive\/2021\/12\/02\/vaccine-reaction-data.aspx\" target=\"_blank\" rel=\"nofollow\">Mercola.com<\/a>.<\/em><\/p>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>It took the U.S. Food and Drug Administration 108 days to review all the data Pfizer\/BioNTech submitted in order to gain FDA approval for its Comirnaty COVID shot, which was licensed August 3, 2021. <\/p>\n<p>Considering the agency claims there are 329,000 pages of data, the fact that they were able to read, analyze and draw conclusions about its safety and effectiveness in just 108 days \u2014 about 80,000 pages a month \u2014 is no small miracle. They must employ some very efficient speed readers.<\/p>\n<p>And that is why the FDA\u2019s claim that it now needs half a century to review the documents before they can release them to the public doesn\u2019t seem very credible. Even Reuters has expressed shock, and its former CEO is on the board of Pfizer.1<\/p>\n<p>Expedited FOIA Request for Comirnaty Data<\/p>\n<p>In September 2021, a group called Public Health and Medical Professionals for Transparency (PHMPT) filed a Freedom of Information Act (FOIA) request with the FDA to obtain the documentation used to approve Comirnaty.<\/p>\n<p>This includes safety and effectiveness data, adverse reaction reports and lists of active and inactive ingredients. Approximately 400 additional FOIA requests by other individuals for all or part of this information have also been filed.2<\/p>\n<p>In their FOIA application, the PHMPT asked the agency to expedite release of the documents \u2014 a reasonable request, considering we have no raw data and the shots are being pushed on children as young as 5.<\/p>\n<p>FOIA guidelines include two conditions upon which a request may be expedited. One is \u201cif the lack of expedited treatment could reasonably be expected to pose a threat to someone\u2019s life or physical safety,\u201d which one could easily argue is the case here.<\/p>\n<p>The second condition is \u201cif there is an urgency to inform the public about an actual or alleged federal government activity, if made by a person who is primarily engaged in disseminating information.\u201d This too is clearly applicable.<\/p>\n<p>\u201cDuring a time when COVID-19 vaccine mandates are being implemented over the objection of those that have questions about the data and information supporting the safety and efficacy of the Pfizer Vaccine, and individuals with these questions are being expelled from employment, school, transportation, and the military, the public has an urgent and immediate need to have access to this data,\u201d the PHMPT said in its request.3<\/p>\n<p>FDA Now Wants 55 Years to Release COVID Jab Data<\/p>\n<p>When, after a month, the FDA still had not responded to the FOIA request, the PHMPT sued.4 The FDA is now asking a federal judge to allow them to delay the full release of all documents until 2076 \u2014 55 years from now.<\/p>\n<p>According to the U.S. Department of Justice (DOJ) attorney who represents the FDA in this case, the agency will be able to \u201cprovide more pages to more requesters\u201d if allowed to stick to a rolling schedule of 500 pages per month, \u201cthus avoiding a system where a few large requests monopolize finite processing resources.\u201d<\/p>\n<p>They claim they only have 10 employees assigned to FOIA releases, and before material can be released, an FDA official has to go through them and redact any information that might reveal personal information about clinical trial participants and any confidential business or trade secret information.<\/p>\n<p>The 1967 FOIA law requires federal agencies to respond to FOIAs within 20 days unless \u201cunusual circumstances\u201d exist that prevent a timely release. Circumstances that might warrant an extended release schedule include:<\/p>\n<p> Instances where response records must be searched for and collected from an entity other than the office processing the request<br \/>\n Situations involving \u201cvoluminous\u201d amounts of records that must be compiled, and<br \/>\n Instances requiring consultation with another federal agency that has a substantial interest in the information<\/p>\n<p>The DOJ attorney points out that the court has allowed for a 500-page maximum per month release schedule in other cases, and should allow the FDA the same leeway here.<\/p>\n<p>While it can conduct that intense review of Pfizer\u2019s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public. ~ Aaron Siri, attorney for PHPMT<\/p>\n<p>Plaintiffs, on the other hand, argue the agency should be able to release everything by early March 2022, noting the FDA employs 18,000 people and has an annual budget of $6 billion. Between 2008 and 2017, the agency processed 114,938 FOIA requests, of which it granted 72.4%, either fully or partially.<\/p>\n<p>Of those, 39.8% were designated as \u201ccomplex,\u201d and 81.5% of these complex FOIA requests were granted in 61 days or more. Considering these historical statistics, a backlog of 400 FOIA requests doesn\u2019t appear excessively burdensome.<\/p>\n<p>FDA\u2019s Foot-Dragging Is Suspicious<\/p>\n<p>Then there\u2019s the sticky issue that it has already proven its capacity for rapid review. Aaron Siri of the law firm Siri &#038; Glimstad wrote in the PHMPT\u2019s court filing:5,6,7,8<\/p>\n<p>\u201cThis 108-day period is the same amount of time it took the FDA to review the responsive documents for the far more intricate task of licensing Pfizer&#8217;s COVID-19 vaccine &#8230;<\/p>\n<p>It took the FDA precisely 108 days from when Pfizer started producing the records for licensure to when the FDA licensed the Pfizer vaccine. Taking the FDA at its word, it conducted an intense, robust, thorough, and complete review and analysis of those documents in order to assure that the Pfizer vaccine was safe and effective for licensure.<\/p>\n<p>While it can conduct that intense review of Pfizer\u2019s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public &#8230;<\/p>\n<p>The entire purpose of the FOIA is to assure government transparency. It is difficult to imagine a greater need for transparency than immediate disclosure of the documents relied upon by the FDA to license a product that is now being mandated to over 100 million Americans under penalty of losing their careers, their income, their military service status, and far worse.\u201d<\/p>\n<p>Shocking Revelations in First Batch of FOIA Docs<\/p>\n<p>Two months after the lawsuit against it was filed, the FDA released a batch of 91 pages,9 and if this batch is any indication, it\u2019s not surprising that the FDA wants to slow-walk the release of the rest. In a November 21, 2021, substack article, Kyle Becker cites directly from the released documents:10<\/p>\n<p>\u201c\u2019It is estimated that approximately [REDACTED] doses of BNT162b2 were shipped worldwide from the receipt of the first temporary authorization for emergency supply on 01 December 2020 through 28 February 2021,\u2019 the document states. \u2018Cumulatively, 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 &#8230;<\/p>\n<p>Most cases (34,762) were received from United States (13,739), United Kingdom (13,404) Italy (2,578), Germany (1913), France (1506), Portugal (866).\u2019 Below is a General Overview of the reported outcomes to the Adverse Events:<\/p>\n<p>The chart lists 1,223 fatal outcomes in the Relevant Cases. Interestingly, the age range with the most relevant cases was 31-50 years old, which is not the age group considered to be at high risk from COVID-19.\u201d<\/p>\n<p>It\u2019s worth noting that by redacting the specified number of doses shipped, it becomes more difficult to assess the potential ratio of injury. Still, even without that, 42,086 reports of injury, including 1,223 fatalities, are a significant signal in and of itself, especially when you consider that the 1976 swine flu vaccine was pulled after 25 deaths.<\/p>\n<p>Glaring Disregard for Life<\/p>\n<p>It\u2019s even more disturbing when you consider that those 42,086 reports were received by Pfizer in just the first 2.5 months of the shot being rolled out. Pfizer even acknowledges the abnormal rate of injuries, but then sweeps it aside as being of no consequence. As noted by Siri, in a November 19, 2021 substack article, in which he discusses this first batch of documents:11<\/p>\n<p>\u201cPfizer explains, on page 6, that \u2018Due to the large numbers of spontaneous adverse event reports received for the product, [Pfizer] has prioritized the processing of serious cases\u2026\u2019<\/p>\n<p>Pfizer \u2018has also taken a [sic] multiple actions to help alleviate the large increase of adverse event reports\u2019 including \u2018increasing the number of data entry and case processing colleagues\u2019 and \u2018has onboarded approximately [REDACTED] additional fulltime employees (FTEs).\u2019<\/p>\n<p>Query why it is proprietary to share how many people Pfizer had to hire to track all of the adverse events being reported shortly after launching its product &#8230;<\/p>\n<p>But no cause for alarm since Pfizer explains to the FDA: \u2018The findings of these signal detection analyses are consistent with the known safety profile of the vaccine.\u2019 So, if they knew these issues were going to arise, then why didn\u2019t they appear to have enough staff to process this expected volume of reports?<\/p>\n<p>The grand conclusion by Pfizer to the FDA: \u2018The data do not reveal any novel safety concerns or risks requiring label changes and support a favorable benefit risk profile of to the BNT162b2 vaccine.\u2019 Nothing to see here.\u201d<\/p>\n<p>Clearly, there\u2019s plenty to be seen in the hundreds of thousands of documents Pfizer\/BioNTech submitted to the FDA. The fact that the FDA is stonewalling and wants 55 years to redact them before they\u2019re fit for public view is telling in and of itself.<\/p>\n<p>You don\u2019t need a fanciful imagination to comprehend what they might be hiding. It almost seems they want to make sure the responsible parties are all dead by the time the full data set is out in the open and people can be held to account for their decisions. Let\u2019s hope the judge is more interested in public health than protecting the FDA\u2019s dirty secrets.<\/p>\n","protected":false},"author":687,"featured_media":168525,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"sfsi_plus_gutenberg_text_before_share":"","sfsi_plus_gutenberg_show_text_before_share":"","sfsi_plus_gutenberg_icon_type":"","sfsi_plus_gutenberg_icon_alignemt":"","sfsi_plus_gutenburg_max_per_row":"","_genesis_hide_title":false,"_genesis_hide_breadcrumbs":false,"_genesis_hide_singular_image":false,"_genesis_hide_footer_widgets":false,"_genesis_custom_body_class":"","_genesis_custom_post_class":"","_genesis_layout":"","footnotes":"","_ppma_block_editor_authors":""},"categories":[359,196],"tags":[],"ppma_author":[657],"class_list":["post-210864","post","type-post","status-publish","format-standard","has-post-thumbnail","category-fda","category-vaccines","entry"],"aioseo_notices":[],"aioseo_head":"\n\t\t<!-- All in One SEO 5.0.2.1 - aioseo.com -->\n\t<meta name=\"description\" content=\"It took the U.S. Food and Drug Administration 108 days to review all the data Pfizer\/BioNTech submitted in order to gain FDA approval for its Comirnaty COVID shot, which was licensed August 3, 2021. Considering the agency claims there are 329,000 pages of data, the fact that they were able to read, analyze and draw conclusions about its safety and effectiveness in just 108 days \u2014 about 80,000 pages a month \u2014 is no small miracle. They must employ some very efficient speed readers. And that is why the FDA\u2019s claim that it now needs half a century to review the documents before they can release them to the public doesn\u2019t seem very credible. Even Reuters has expressed shock, and its former CEO is on the board of Pfizer.1 Expedited FOIA Request for Comirnaty Data In September 2021, a group called Public Health and Medical Professionals for Transparency (PHMPT) filed a Freedom of Information Act (FOIA) request with the FDA to obtain the documentation used to approve Comirnaty. This includes safety and effectiveness data, adverse reaction reports and lists of active and inactive ingredients. Approximately 400 additional FOIA requests by other individuals for all or part of this information have also been filed.2 In their FOIA application, the PHMPT asked the agency to expedite release of the documents \u2014 a reasonable request, considering we have no raw data and the shots are being pushed on children as young as 5. FOIA guidelines include two conditions upon which a request may be expedited. One is \u201cif the lack of expedited treatment could reasonably be expected to pose a threat to someone\u2019s life or physical safety,\u201d which one could easily argue is the case here. The second condition is \u201cif there is an urgency to inform the public about an actual or alleged federal government activity, if made by a person who is primarily engaged in disseminating information.\u201d This too is clearly applicable. \u201cDuring a time when COVID-19 vaccine mandates are being implemented over the objection of those that have questions about the data and information supporting the safety and efficacy of the Pfizer Vaccine, and individuals with these questions are being expelled from employment, school, transportation, and the military, the public has an urgent and immediate need to have access to this data,\u201d the PHMPT said in its request.3 FDA Now Wants 55 Years to Release COVID Jab Data When, after a month, the FDA still had not responded to the FOIA request, the PHMPT sued.4 The FDA is now asking a federal judge to allow them to delay the full release of all documents until 2076 \u2014 55 years from now. According to the U.S. Department of Justice (DOJ) attorney who represents the FDA in this case, the agency will be able to \u201cprovide more pages to more requesters\u201d if allowed to stick to a rolling schedule of 500 pages per month, \u201cthus avoiding a system where a few large requests monopolize finite processing resources.\u201d They claim they only have 10 employees assigned to FOIA releases, and before material can be released, an FDA official has to go through them and redact any information that might reveal personal information about clinical trial participants and any confidential business or trade secret information. The 1967 FOIA law requires federal agencies to respond to FOIAs within 20 days unless \u201cunusual circumstances\u201d exist that prevent a timely release. Circumstances that might warrant an extended release schedule include: Instances where response records must be searched for and collected from an entity other than the office processing the request Situations involving \u201cvoluminous\u201d amounts of records that must be compiled, and Instances requiring consultation with another federal agency that has a substantial interest in the information The DOJ attorney points out that the court has allowed for a 500-page maximum per month release schedule in other cases, and should allow the FDA the same leeway here. While it can conduct that intense review of Pfizer\u2019s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public. ~ Aaron Siri, attorney for PHPMT Plaintiffs, on the other hand, argue the agency should be able to release everything by early March 2022, noting the FDA employs 18,000 people and has an annual budget of $6 billion. Between 2008 and 2017, the agency processed 114,938 FOIA requests, of which it granted 72.4%, either fully or partially. Of those, 39.8% were designated as \u201ccomplex,\u201d and 81.5% of these complex FOIA requests were granted in 61 days or more. Considering these historical statistics, a backlog of 400 FOIA requests doesn\u2019t appear excessively burdensome. FDA\u2019s Foot-Dragging Is Suspicious Then there\u2019s the sticky issue that it has already proven its capacity for rapid review. Aaron Siri of the law firm Siri &amp; Glimstad wrote in the PHMPT\u2019s court filing:5,6,7,8 \u201cThis 108-day period is the same amount of time it took the FDA to review the responsive documents for the far more intricate task of licensing Pfizer&#039;s COVID-19 vaccine ... It took the FDA precisely 108 days from when Pfizer started producing the records for licensure to when the FDA licensed the Pfizer vaccine. Taking the FDA at its word, it conducted an intense, robust, thorough, and complete review and analysis of those documents in order to assure that the Pfizer vaccine was safe and effective for licensure. While it can conduct that intense review of Pfizer\u2019s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public ... The entire purpose of the FOIA is to assure government transparency. It is difficult to imagine a greater need for transparency than immediate disclosure of the documents relied upon by the FDA to license a product that is now being mandated to over 100 million Americans under penalty of losing their careers, their income, their military service status, and far worse.\u201d Shocking Revelations in First Batch of FOIA Docs Two months after the lawsuit against it was filed, the FDA released a batch of 91 pages,9 and if this batch is any indication, it\u2019s not surprising that the FDA wants to slow-walk the release of the rest. In a November 21, 2021, substack article, Kyle Becker cites directly from the released documents:10 \u201c\u2019It is estimated that approximately [REDACTED] doses of BNT162b2 were shipped worldwide from the receipt of the first temporary authorization for emergency supply on 01 December 2020 through 28 February 2021,\u2019 the document states. \u2018Cumulatively, 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).\u2019 Below is a General Overview of the reported outcomes to the Adverse Events: The chart lists 1,223 fatal outcomes in the Relevant Cases. Interestingly, the age range with the most relevant cases was 31-50 years old, which is not the age group considered to be at high risk from COVID-19.\u201d It\u2019s worth noting that by redacting the specified number of doses shipped, it becomes more difficult to assess the potential ratio of injury. Still, even without that, 42,086 reports of injury, including 1,223 fatalities, are a significant signal in and of itself, especially when you consider that the 1976 swine flu vaccine was pulled after 25 deaths. Glaring Disregard for Life It\u2019s even more disturbing when you consider that those 42,086 reports were received by Pfizer in just the first 2.5 months of the shot being rolled out. Pfizer even acknowledges the abnormal rate of injuries, but then sweeps it aside as being of no consequence. As noted by Siri, in a November 19, 2021 substack article, in which he discusses this first batch of documents:11 \u201cPfizer explains, on page 6, that \u2018Due to the large numbers of spontaneous adverse event reports received for the product, [Pfizer] has prioritized the processing of serious cases\u2026\u2019 Pfizer \u2018has also taken a [sic] multiple actions to help alleviate the large increase of adverse event reports\u2019 including \u2018increasing the number of data entry and case processing colleagues\u2019 and \u2018has onboarded approximately [REDACTED] additional fulltime employees (FTEs).\u2019 Query why it is proprietary to share how many people Pfizer had to hire to track all of the adverse events being reported shortly after launching its product ... But no cause for alarm since Pfizer explains to the FDA: \u2018The findings of these signal detection analyses are consistent with the known safety profile of the vaccine.\u2019 So, if they knew these issues were going to arise, then why didn\u2019t they appear to have enough staff to process this expected volume of reports? The grand conclusion by Pfizer to the FDA: \u2018The data do not reveal any novel safety concerns or risks requiring label changes and support a favorable benefit risk profile of to the BNT162b2 vaccine.\u2019 Nothing to see here.\u201d Clearly, there\u2019s plenty to be seen in the hundreds of thousands of documents Pfizer\/BioNTech submitted to the FDA. The fact that the FDA is stonewalling and wants 55 years to redact them before they\u2019re fit for public view is telling in and of itself. You don\u2019t need a fanciful imagination to comprehend what they might be hiding. It almost seems they want to make sure the responsible parties are all dead by the time the full data set is out in the open and people can be held to account for their decisions. Let\u2019s hope the judge is more interested in public health than protecting the FDA\u2019s dirty secrets.\" \/>\n\t<meta name=\"robots\" content=\"max-image-preview:large\" \/>\n\t<meta name=\"author\" content=\"Dr Joseph Mercola\"\/>\n\t<link rel=\"canonical\" href=\"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/\" \/>\n\t<meta name=\"generator\" content=\"All in One SEO (AIOSEO) 5.0.2.1\" \/>\n\t\t<script type=\"application\/ld+json\" class=\"aioseo-schema\">\n\t\t\t{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/z3news.com\\\/w\\\/fda-wants-55-years-to-release-covid-jab-reaction-data\\\/#article\",\"name\":\"FDA Wants 55 Years to Release COVID Jab Reaction Data | Z3 News\",\"headline\":\"FDA Wants 55 Years to Release COVID Jab Reaction 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News\",\"description\":\"It took the U.S. Food and Drug Administration 108 days to review all the data Pfizer\\\/BioNTech submitted in order to gain FDA approval for its Comirnaty COVID shot, which was licensed August 3, 2021. Considering the agency claims there are 329,000 pages of data, the fact that they were able to read, analyze and draw conclusions about its safety and effectiveness in just 108 days \\u2014 about 80,000 pages a month \\u2014 is no small miracle. They must employ some very efficient speed readers. And that is why the FDA\\u2019s claim that it now needs half a century to review the documents before they can release them to the public doesn\\u2019t seem very credible. Even Reuters has expressed shock, and its former CEO is on the board of Pfizer.1 Expedited FOIA Request for Comirnaty Data In September 2021, a group called Public Health and Medical Professionals for Transparency (PHMPT) filed a Freedom of Information Act (FOIA) request with the FDA to obtain the documentation used to approve Comirnaty. This includes safety and effectiveness data, adverse reaction reports and lists of active and inactive ingredients. Approximately 400 additional FOIA requests by other individuals for all or part of this information have also been filed.2 In their FOIA application, the PHMPT asked the agency to expedite release of the documents \\u2014 a reasonable request, considering we have no raw data and the shots are being pushed on children as young as 5. FOIA guidelines include two conditions upon which a request may be expedited. One is \\u201cif the lack of expedited treatment could reasonably be expected to pose a threat to someone\\u2019s life or physical safety,\\u201d which one could easily argue is the case here. The second condition is \\u201cif there is an urgency to inform the public about an actual or alleged federal government activity, if made by a person who is primarily engaged in disseminating information.\\u201d This too is clearly applicable. \\u201cDuring a time when COVID-19 vaccine mandates are being implemented over the objection of those that have questions about the data and information supporting the safety and efficacy of the Pfizer Vaccine, and individuals with these questions are being expelled from employment, school, transportation, and the military, the public has an urgent and immediate need to have access to this data,\\u201d the PHMPT said in its request.3 FDA Now Wants 55 Years to Release COVID Jab Data When, after a month, the FDA still had not responded to the FOIA request, the PHMPT sued.4 The FDA is now asking a federal judge to allow them to delay the full release of all documents until 2076 \\u2014 55 years from now. According to the U.S. Department of Justice (DOJ) attorney who represents the FDA in this case, the agency will be able to \\u201cprovide more pages to more requesters\\u201d if allowed to stick to a rolling schedule of 500 pages per month, \\u201cthus avoiding a system where a few large requests monopolize finite processing resources.\\u201d They claim they only have 10 employees assigned to FOIA releases, and before material can be released, an FDA official has to go through them and redact any information that might reveal personal information about clinical trial participants and any confidential business or trade secret information. The 1967 FOIA law requires federal agencies to respond to FOIAs within 20 days unless \\u201cunusual circumstances\\u201d exist that prevent a timely release. Circumstances that might warrant an extended release schedule include: Instances where response records must be searched for and collected from an entity other than the office processing the request Situations involving \\u201cvoluminous\\u201d amounts of records that must be compiled, and Instances requiring consultation with another federal agency that has a substantial interest in the information The DOJ attorney points out that the court has allowed for a 500-page maximum per month release schedule in other cases, and should allow the FDA the same leeway here. While it can conduct that intense review of Pfizer\\u2019s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public. ~ Aaron Siri, attorney for PHPMT Plaintiffs, on the other hand, argue the agency should be able to release everything by early March 2022, noting the FDA employs 18,000 people and has an annual budget of $6 billion. Between 2008 and 2017, the agency processed 114,938 FOIA requests, of which it granted 72.4%, either fully or partially. Of those, 39.8% were designated as \\u201ccomplex,\\u201d and 81.5% of these complex FOIA requests were granted in 61 days or more. Considering these historical statistics, a backlog of 400 FOIA requests doesn\\u2019t appear excessively burdensome. FDA\\u2019s Foot-Dragging Is Suspicious Then there\\u2019s the sticky issue that it has already proven its capacity for rapid review. Aaron Siri of the law firm Siri & Glimstad wrote in the PHMPT\\u2019s court filing:5,6,7,8 \\u201cThis 108-day period is the same amount of time it took the FDA to review the responsive documents for the far more intricate task of licensing Pfizer's COVID-19 vaccine ... It took the FDA precisely 108 days from when Pfizer started producing the records for licensure to when the FDA licensed the Pfizer vaccine. Taking the FDA at its word, it conducted an intense, robust, thorough, and complete review and analysis of those documents in order to assure that the Pfizer vaccine was safe and effective for licensure. While it can conduct that intense review of Pfizer\\u2019s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public ... The entire purpose of the FOIA is to assure government transparency. It is difficult to imagine a greater need for transparency than immediate disclosure of the documents relied upon by the FDA to license a product that is now being mandated to over 100 million Americans under penalty of losing their careers, their income, their military service status, and far worse.\\u201d Shocking Revelations in First Batch of FOIA Docs Two months after the lawsuit against it was filed, the FDA released a batch of 91 pages,9 and if this batch is any indication, it\\u2019s not surprising that the FDA wants to slow-walk the release of the rest. In a November 21, 2021, substack article, Kyle Becker cites directly from the released documents:10 \\u201c\\u2019It is estimated that approximately [REDACTED] doses of BNT162b2 were shipped worldwide from the receipt of the first temporary authorization for emergency supply on 01 December 2020 through 28 February 2021,\\u2019 the document states. \\u2018Cumulatively, 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).\\u2019 Below is a General Overview of the reported outcomes to the Adverse Events: The chart lists 1,223 fatal outcomes in the Relevant Cases. Interestingly, the age range with the most relevant cases was 31-50 years old, which is not the age group considered to be at high risk from COVID-19.\\u201d It\\u2019s worth noting that by redacting the specified number of doses shipped, it becomes more difficult to assess the potential ratio of injury. Still, even without that, 42,086 reports of injury, including 1,223 fatalities, are a significant signal in and of itself, especially when you consider that the 1976 swine flu vaccine was pulled after 25 deaths. Glaring Disregard for Life It\\u2019s even more disturbing when you consider that those 42,086 reports were received by Pfizer in just the first 2.5 months of the shot being rolled out. Pfizer even acknowledges the abnormal rate of injuries, but then sweeps it aside as being of no consequence. As noted by Siri, in a November 19, 2021 substack article, in which he discusses this first batch of documents:11 \\u201cPfizer explains, on page 6, that \\u2018Due to the large numbers of spontaneous adverse event reports received for the product, [Pfizer] has prioritized the processing of serious cases\\u2026\\u2019 Pfizer \\u2018has also taken a [sic] multiple actions to help alleviate the large increase of adverse event reports\\u2019 including \\u2018increasing the number of data entry and case processing colleagues\\u2019 and \\u2018has onboarded approximately [REDACTED] additional fulltime employees (FTEs).\\u2019 Query why it is proprietary to share how many people Pfizer had to hire to track all of the adverse events being reported shortly after launching its product ... But no cause for alarm since Pfizer explains to the FDA: \\u2018The findings of these signal detection analyses are consistent with the known safety profile of the vaccine.\\u2019 So, if they knew these issues were going to arise, then why didn\\u2019t they appear to have enough staff to process this expected volume of reports? The grand conclusion by Pfizer to the FDA: \\u2018The data do not reveal any novel safety concerns or risks requiring label changes and support a favorable benefit risk profile of to the BNT162b2 vaccine.\\u2019 Nothing to see here.\\u201d Clearly, there\\u2019s plenty to be seen in the hundreds of thousands of documents Pfizer\\\/BioNTech submitted to the FDA. The fact that the FDA is stonewalling and wants 55 years to redact them before they\\u2019re fit for public view is telling in and of itself. You don\\u2019t need a fanciful imagination to comprehend what they might be hiding. It almost seems they want to make sure the responsible parties are all dead by the time the full data set is out in the open and people can be held to account for their decisions. Let\\u2019s hope the judge is more interested in public health than protecting the FDA\\u2019s dirty secrets.\",\"inLanguage\":\"en-US\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/z3news.com\\\/w\\\/#website\"},\"breadcrumb\":{\"@id\":\"https:\\\/\\\/z3news.com\\\/w\\\/fda-wants-55-years-to-release-covid-jab-reaction-data\\\/#breadcrumblist\"},\"author\":{\"@id\":\"https:\\\/\\\/z3news.com\\\/w\\\/author\\\/mercola\\\/#author\"},\"creator\":{\"@id\":\"https:\\\/\\\/z3news.com\\\/w\\\/author\\\/mercola\\\/#author\"},\"image\":{\"@type\":\"ImageObject\",\"url\":\"https:\\\/\\\/z3news.com\\\/w\\\/wp-content\\\/uploads\\\/2021\\\/05\\\/C43D8472-9106-40FB-B345-054F888B9355.jpeg\",\"@id\":\"https:\\\/\\\/z3news.com\\\/w\\\/fda-wants-55-years-to-release-covid-jab-reaction-data\\\/#mainImage\",\"width\":500,\"height\":500},\"primaryImageOfPage\":{\"@id\":\"https:\\\/\\\/z3news.com\\\/w\\\/fda-wants-55-years-to-release-covid-jab-reaction-data\\\/#mainImage\"},\"datePublished\":\"2021-12-01T19:00:00-05:00\",\"dateModified\":\"2021-12-02T15:17:05-05:00\"},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/z3news.com\\\/w\\\/#website\",\"url\":\"https:\\\/\\\/z3news.com\\\/w\\\/\",\"name\":\"Z3 News\",\"description\":\"Revealing Mystery Babylon\",\"inLanguage\":\"en-US\",\"publisher\":{\"@id\":\"https:\\\/\\\/z3news.com\\\/w\\\/#organization\"}}]}\n\t\t<\/script>\n\t\t<!-- All in One SEO -->\n\n","aioseo_head_json":{"title":"FDA Wants 55 Years to Release COVID Jab Reaction Data | Z3 News","description":"It took the U.S. Food and Drug Administration 108 days to review all the data Pfizer\/BioNTech submitted in order to gain FDA approval for its Comirnaty COVID shot, which was licensed August 3, 2021. Considering the agency claims there are 329,000 pages of data, the fact that they were able to read, analyze and draw conclusions about its safety and effectiveness in just 108 days \u2014 about 80,000 pages a month \u2014 is no small miracle. They must employ some very efficient speed readers. And that is why the FDA\u2019s claim that it now needs half a century to review the documents before they can release them to the public doesn\u2019t seem very credible. Even Reuters has expressed shock, and its former CEO is on the board of Pfizer.1 Expedited FOIA Request for Comirnaty Data In September 2021, a group called Public Health and Medical Professionals for Transparency (PHMPT) filed a Freedom of Information Act (FOIA) request with the FDA to obtain the documentation used to approve Comirnaty. This includes safety and effectiveness data, adverse reaction reports and lists of active and inactive ingredients. Approximately 400 additional FOIA requests by other individuals for all or part of this information have also been filed.2 In their FOIA application, the PHMPT asked the agency to expedite release of the documents \u2014 a reasonable request, considering we have no raw data and the shots are being pushed on children as young as 5. FOIA guidelines include two conditions upon which a request may be expedited. One is \u201cif the lack of expedited treatment could reasonably be expected to pose a threat to someone\u2019s life or physical safety,\u201d which one could easily argue is the case here. The second condition is \u201cif there is an urgency to inform the public about an actual or alleged federal government activity, if made by a person who is primarily engaged in disseminating information.\u201d This too is clearly applicable. \u201cDuring a time when COVID-19 vaccine mandates are being implemented over the objection of those that have questions about the data and information supporting the safety and efficacy of the Pfizer Vaccine, and individuals with these questions are being expelled from employment, school, transportation, and the military, the public has an urgent and immediate need to have access to this data,\u201d the PHMPT said in its request.3 FDA Now Wants 55 Years to Release COVID Jab Data When, after a month, the FDA still had not responded to the FOIA request, the PHMPT sued.4 The FDA is now asking a federal judge to allow them to delay the full release of all documents until 2076 \u2014 55 years from now. According to the U.S. Department of Justice (DOJ) attorney who represents the FDA in this case, the agency will be able to \u201cprovide more pages to more requesters\u201d if allowed to stick to a rolling schedule of 500 pages per month, \u201cthus avoiding a system where a few large requests monopolize finite processing resources.\u201d They claim they only have 10 employees assigned to FOIA releases, and before material can be released, an FDA official has to go through them and redact any information that might reveal personal information about clinical trial participants and any confidential business or trade secret information. The 1967 FOIA law requires federal agencies to respond to FOIAs within 20 days unless \u201cunusual circumstances\u201d exist that prevent a timely release. Circumstances that might warrant an extended release schedule include: Instances where response records must be searched for and collected from an entity other than the office processing the request Situations involving \u201cvoluminous\u201d amounts of records that must be compiled, and Instances requiring consultation with another federal agency that has a substantial interest in the information The DOJ attorney points out that the court has allowed for a 500-page maximum per month release schedule in other cases, and should allow the FDA the same leeway here. While it can conduct that intense review of Pfizer\u2019s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public. ~ Aaron Siri, attorney for PHPMT Plaintiffs, on the other hand, argue the agency should be able to release everything by early March 2022, noting the FDA employs 18,000 people and has an annual budget of $6 billion. Between 2008 and 2017, the agency processed 114,938 FOIA requests, of which it granted 72.4%, either fully or partially. Of those, 39.8% were designated as \u201ccomplex,\u201d and 81.5% of these complex FOIA requests were granted in 61 days or more. Considering these historical statistics, a backlog of 400 FOIA requests doesn\u2019t appear excessively burdensome. FDA\u2019s Foot-Dragging Is Suspicious Then there\u2019s the sticky issue that it has already proven its capacity for rapid review. Aaron Siri of the law firm Siri & Glimstad wrote in the PHMPT\u2019s court filing:5,6,7,8 \u201cThis 108-day period is the same amount of time it took the FDA to review the responsive documents for the far more intricate task of licensing Pfizer's COVID-19 vaccine ... It took the FDA precisely 108 days from when Pfizer started producing the records for licensure to when the FDA licensed the Pfizer vaccine. Taking the FDA at its word, it conducted an intense, robust, thorough, and complete review and analysis of those documents in order to assure that the Pfizer vaccine was safe and effective for licensure. While it can conduct that intense review of Pfizer\u2019s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public ... The entire purpose of the FOIA is to assure government transparency. It is difficult to imagine a greater need for transparency than immediate disclosure of the documents relied upon by the FDA to license a product that is now being mandated to over 100 million Americans under penalty of losing their careers, their income, their military service status, and far worse.\u201d Shocking Revelations in First Batch of FOIA Docs Two months after the lawsuit against it was filed, the FDA released a batch of 91 pages,9 and if this batch is any indication, it\u2019s not surprising that the FDA wants to slow-walk the release of the rest. In a November 21, 2021, substack article, Kyle Becker cites directly from the released documents:10 \u201c\u2019It is estimated that approximately [REDACTED] doses of BNT162b2 were shipped worldwide from the receipt of the first temporary authorization for emergency supply on 01 December 2020 through 28 February 2021,\u2019 the document states. \u2018Cumulatively, 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).\u2019 Below is a General Overview of the reported outcomes to the Adverse Events: The chart lists 1,223 fatal outcomes in the Relevant Cases. Interestingly, the age range with the most relevant cases was 31-50 years old, which is not the age group considered to be at high risk from COVID-19.\u201d It\u2019s worth noting that by redacting the specified number of doses shipped, it becomes more difficult to assess the potential ratio of injury. Still, even without that, 42,086 reports of injury, including 1,223 fatalities, are a significant signal in and of itself, especially when you consider that the 1976 swine flu vaccine was pulled after 25 deaths. Glaring Disregard for Life It\u2019s even more disturbing when you consider that those 42,086 reports were received by Pfizer in just the first 2.5 months of the shot being rolled out. Pfizer even acknowledges the abnormal rate of injuries, but then sweeps it aside as being of no consequence. As noted by Siri, in a November 19, 2021 substack article, in which he discusses this first batch of documents:11 \u201cPfizer explains, on page 6, that \u2018Due to the large numbers of spontaneous adverse event reports received for the product, [Pfizer] has prioritized the processing of serious cases\u2026\u2019 Pfizer \u2018has also taken a [sic] multiple actions to help alleviate the large increase of adverse event reports\u2019 including \u2018increasing the number of data entry and case processing colleagues\u2019 and \u2018has onboarded approximately [REDACTED] additional fulltime employees (FTEs).\u2019 Query why it is proprietary to share how many people Pfizer had to hire to track all of the adverse events being reported shortly after launching its product ... But no cause for alarm since Pfizer explains to the FDA: \u2018The findings of these signal detection analyses are consistent with the known safety profile of the vaccine.\u2019 So, if they knew these issues were going to arise, then why didn\u2019t they appear to have enough staff to process this expected volume of reports? The grand conclusion by Pfizer to the FDA: \u2018The data do not reveal any novel safety concerns or risks requiring label changes and support a favorable benefit risk profile of to the BNT162b2 vaccine.\u2019 Nothing to see here.\u201d Clearly, there\u2019s plenty to be seen in the hundreds of thousands of documents Pfizer\/BioNTech submitted to the FDA. The fact that the FDA is stonewalling and wants 55 years to redact them before they\u2019re fit for public view is telling in and of itself. You don\u2019t need a fanciful imagination to comprehend what they might be hiding. It almost seems they want to make sure the responsible parties are all dead by the time the full data set is out in the open and people can be held to account for their decisions. Let\u2019s hope the judge is more interested in public health than protecting the FDA\u2019s dirty secrets.","canonical_url":"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/","robots":"max-image-preview:large","keywords":"","webmasterTools":{"miscellaneous":""},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/#article","name":"FDA Wants 55 Years to Release COVID Jab Reaction Data | Z3 News","headline":"FDA Wants 55 Years to Release COVID Jab Reaction Data","author":{"@id":"https:\/\/z3news.com\/w\/author\/mercola\/#author"},"publisher":{"@id":"https:\/\/z3news.com\/w\/#organization"},"image":{"@type":"ImageObject","url":"https:\/\/z3news.com\/w\/wp-content\/uploads\/2021\/05\/C43D8472-9106-40FB-B345-054F888B9355.jpeg","width":500,"height":500},"datePublished":"2021-12-01T19:00:00-05:00","dateModified":"2021-12-02T15:17:05-05:00","inLanguage":"en-US","mainEntityOfPage":{"@id":"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/#webpage"},"isPartOf":{"@id":"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/#webpage"},"articleSection":"FDA, Vaccines, Dr Joseph Mercola"},{"@type":"BreadcrumbList","@id":"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/#breadcrumblist","itemListElement":[{"@type":"ListItem","@id":"https:\/\/z3news.com\/w\/#listItem","position":1,"name":"Home","item":"https:\/\/z3news.com\/w\/","nextItem":{"@type":"ListItem","@id":"https:\/\/z3news.com\/w\/category\/news\/#listItem","name":"News"}},{"@type":"ListItem","@id":"https:\/\/z3news.com\/w\/category\/news\/#listItem","position":2,"name":"News","item":"https:\/\/z3news.com\/w\/category\/news\/","nextItem":{"@type":"ListItem","@id":"https:\/\/z3news.com\/w\/category\/news\/jesuit-led-organizations\/#listItem","name":"Jesuit Controlled Organizations"},"previousItem":{"@type":"ListItem","@id":"https:\/\/z3news.com\/w\/#listItem","name":"Home"}},{"@type":"ListItem","@id":"https:\/\/z3news.com\/w\/category\/news\/jesuit-led-organizations\/#listItem","position":3,"name":"Jesuit Controlled Organizations","item":"https:\/\/z3news.com\/w\/category\/news\/jesuit-led-organizations\/","nextItem":{"@type":"ListItem","@id":"https:\/\/z3news.com\/w\/category\/news\/jesuit-led-organizations\/fda\/#listItem","name":"FDA"},"previousItem":{"@type":"ListItem","@id":"https:\/\/z3news.com\/w\/category\/news\/#listItem","name":"News"}},{"@type":"ListItem","@id":"https:\/\/z3news.com\/w\/category\/news\/jesuit-led-organizations\/fda\/#listItem","position":4,"name":"FDA","item":"https:\/\/z3news.com\/w\/category\/news\/jesuit-led-organizations\/fda\/","nextItem":{"@type":"ListItem","@id":"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/#listItem","name":"FDA Wants 55 Years to Release COVID Jab Reaction Data"},"previousItem":{"@type":"ListItem","@id":"https:\/\/z3news.com\/w\/category\/news\/jesuit-led-organizations\/#listItem","name":"Jesuit Controlled Organizations"}},{"@type":"ListItem","@id":"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/#listItem","position":5,"name":"FDA Wants 55 Years to Release COVID Jab Reaction Data","previousItem":{"@type":"ListItem","@id":"https:\/\/z3news.com\/w\/category\/news\/jesuit-led-organizations\/fda\/#listItem","name":"FDA"}}]},{"@type":"Organization","@id":"https:\/\/z3news.com\/w\/#organization","name":"Z3 News","description":"Revealing Mystery Babylon","url":"https:\/\/z3news.com\/w\/","logo":{"@type":"ImageObject","url":"https:\/\/z3news.com\/w\/wp-content\/uploads\/2020\/02\/cropped-Z3_tagline.jpeg","@id":"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/#organizationLogo","width":760,"height":180},"image":{"@id":"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/#organizationLogo"}},{"@type":"Person","@id":"https:\/\/z3news.com\/w\/author\/mercola\/#author","url":"https:\/\/z3news.com\/w\/author\/mercola\/","name":"Dr Joseph Mercola"},{"@type":"WebPage","@id":"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/#webpage","url":"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/","name":"FDA Wants 55 Years to Release COVID Jab Reaction Data | Z3 News","description":"It took the U.S. Food and Drug Administration 108 days to review all the data Pfizer\/BioNTech submitted in order to gain FDA approval for its Comirnaty COVID shot, which was licensed August 3, 2021. Considering the agency claims there are 329,000 pages of data, the fact that they were able to read, analyze and draw conclusions about its safety and effectiveness in just 108 days \u2014 about 80,000 pages a month \u2014 is no small miracle. They must employ some very efficient speed readers. And that is why the FDA\u2019s claim that it now needs half a century to review the documents before they can release them to the public doesn\u2019t seem very credible. Even Reuters has expressed shock, and its former CEO is on the board of Pfizer.1 Expedited FOIA Request for Comirnaty Data In September 2021, a group called Public Health and Medical Professionals for Transparency (PHMPT) filed a Freedom of Information Act (FOIA) request with the FDA to obtain the documentation used to approve Comirnaty. This includes safety and effectiveness data, adverse reaction reports and lists of active and inactive ingredients. Approximately 400 additional FOIA requests by other individuals for all or part of this information have also been filed.2 In their FOIA application, the PHMPT asked the agency to expedite release of the documents \u2014 a reasonable request, considering we have no raw data and the shots are being pushed on children as young as 5. FOIA guidelines include two conditions upon which a request may be expedited. One is \u201cif the lack of expedited treatment could reasonably be expected to pose a threat to someone\u2019s life or physical safety,\u201d which one could easily argue is the case here. The second condition is \u201cif there is an urgency to inform the public about an actual or alleged federal government activity, if made by a person who is primarily engaged in disseminating information.\u201d This too is clearly applicable. \u201cDuring a time when COVID-19 vaccine mandates are being implemented over the objection of those that have questions about the data and information supporting the safety and efficacy of the Pfizer Vaccine, and individuals with these questions are being expelled from employment, school, transportation, and the military, the public has an urgent and immediate need to have access to this data,\u201d the PHMPT said in its request.3 FDA Now Wants 55 Years to Release COVID Jab Data When, after a month, the FDA still had not responded to the FOIA request, the PHMPT sued.4 The FDA is now asking a federal judge to allow them to delay the full release of all documents until 2076 \u2014 55 years from now. According to the U.S. Department of Justice (DOJ) attorney who represents the FDA in this case, the agency will be able to \u201cprovide more pages to more requesters\u201d if allowed to stick to a rolling schedule of 500 pages per month, \u201cthus avoiding a system where a few large requests monopolize finite processing resources.\u201d They claim they only have 10 employees assigned to FOIA releases, and before material can be released, an FDA official has to go through them and redact any information that might reveal personal information about clinical trial participants and any confidential business or trade secret information. The 1967 FOIA law requires federal agencies to respond to FOIAs within 20 days unless \u201cunusual circumstances\u201d exist that prevent a timely release. Circumstances that might warrant an extended release schedule include: Instances where response records must be searched for and collected from an entity other than the office processing the request Situations involving \u201cvoluminous\u201d amounts of records that must be compiled, and Instances requiring consultation with another federal agency that has a substantial interest in the information The DOJ attorney points out that the court has allowed for a 500-page maximum per month release schedule in other cases, and should allow the FDA the same leeway here. While it can conduct that intense review of Pfizer\u2019s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public. ~ Aaron Siri, attorney for PHPMT Plaintiffs, on the other hand, argue the agency should be able to release everything by early March 2022, noting the FDA employs 18,000 people and has an annual budget of $6 billion. Between 2008 and 2017, the agency processed 114,938 FOIA requests, of which it granted 72.4%, either fully or partially. Of those, 39.8% were designated as \u201ccomplex,\u201d and 81.5% of these complex FOIA requests were granted in 61 days or more. Considering these historical statistics, a backlog of 400 FOIA requests doesn\u2019t appear excessively burdensome. FDA\u2019s Foot-Dragging Is Suspicious Then there\u2019s the sticky issue that it has already proven its capacity for rapid review. Aaron Siri of the law firm Siri & Glimstad wrote in the PHMPT\u2019s court filing:5,6,7,8 \u201cThis 108-day period is the same amount of time it took the FDA to review the responsive documents for the far more intricate task of licensing Pfizer's COVID-19 vaccine ... It took the FDA precisely 108 days from when Pfizer started producing the records for licensure to when the FDA licensed the Pfizer vaccine. Taking the FDA at its word, it conducted an intense, robust, thorough, and complete review and analysis of those documents in order to assure that the Pfizer vaccine was safe and effective for licensure. While it can conduct that intense review of Pfizer\u2019s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public ... The entire purpose of the FOIA is to assure government transparency. It is difficult to imagine a greater need for transparency than immediate disclosure of the documents relied upon by the FDA to license a product that is now being mandated to over 100 million Americans under penalty of losing their careers, their income, their military service status, and far worse.\u201d Shocking Revelations in First Batch of FOIA Docs Two months after the lawsuit against it was filed, the FDA released a batch of 91 pages,9 and if this batch is any indication, it\u2019s not surprising that the FDA wants to slow-walk the release of the rest. In a November 21, 2021, substack article, Kyle Becker cites directly from the released documents:10 \u201c\u2019It is estimated that approximately [REDACTED] doses of BNT162b2 were shipped worldwide from the receipt of the first temporary authorization for emergency supply on 01 December 2020 through 28 February 2021,\u2019 the document states. \u2018Cumulatively, 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).\u2019 Below is a General Overview of the reported outcomes to the Adverse Events: The chart lists 1,223 fatal outcomes in the Relevant Cases. Interestingly, the age range with the most relevant cases was 31-50 years old, which is not the age group considered to be at high risk from COVID-19.\u201d It\u2019s worth noting that by redacting the specified number of doses shipped, it becomes more difficult to assess the potential ratio of injury. Still, even without that, 42,086 reports of injury, including 1,223 fatalities, are a significant signal in and of itself, especially when you consider that the 1976 swine flu vaccine was pulled after 25 deaths. Glaring Disregard for Life It\u2019s even more disturbing when you consider that those 42,086 reports were received by Pfizer in just the first 2.5 months of the shot being rolled out. Pfizer even acknowledges the abnormal rate of injuries, but then sweeps it aside as being of no consequence. As noted by Siri, in a November 19, 2021 substack article, in which he discusses this first batch of documents:11 \u201cPfizer explains, on page 6, that \u2018Due to the large numbers of spontaneous adverse event reports received for the product, [Pfizer] has prioritized the processing of serious cases\u2026\u2019 Pfizer \u2018has also taken a [sic] multiple actions to help alleviate the large increase of adverse event reports\u2019 including \u2018increasing the number of data entry and case processing colleagues\u2019 and \u2018has onboarded approximately [REDACTED] additional fulltime employees (FTEs).\u2019 Query why it is proprietary to share how many people Pfizer had to hire to track all of the adverse events being reported shortly after launching its product ... But no cause for alarm since Pfizer explains to the FDA: \u2018The findings of these signal detection analyses are consistent with the known safety profile of the vaccine.\u2019 So, if they knew these issues were going to arise, then why didn\u2019t they appear to have enough staff to process this expected volume of reports? The grand conclusion by Pfizer to the FDA: \u2018The data do not reveal any novel safety concerns or risks requiring label changes and support a favorable benefit risk profile of to the BNT162b2 vaccine.\u2019 Nothing to see here.\u201d Clearly, there\u2019s plenty to be seen in the hundreds of thousands of documents Pfizer\/BioNTech submitted to the FDA. The fact that the FDA is stonewalling and wants 55 years to redact them before they\u2019re fit for public view is telling in and of itself. You don\u2019t need a fanciful imagination to comprehend what they might be hiding. It almost seems they want to make sure the responsible parties are all dead by the time the full data set is out in the open and people can be held to account for their decisions. Let\u2019s hope the judge is more interested in public health than protecting the FDA\u2019s dirty secrets.","inLanguage":"en-US","isPartOf":{"@id":"https:\/\/z3news.com\/w\/#website"},"breadcrumb":{"@id":"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/#breadcrumblist"},"author":{"@id":"https:\/\/z3news.com\/w\/author\/mercola\/#author"},"creator":{"@id":"https:\/\/z3news.com\/w\/author\/mercola\/#author"},"image":{"@type":"ImageObject","url":"https:\/\/z3news.com\/w\/wp-content\/uploads\/2021\/05\/C43D8472-9106-40FB-B345-054F888B9355.jpeg","@id":"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/#mainImage","width":500,"height":500},"primaryImageOfPage":{"@id":"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/#mainImage"},"datePublished":"2021-12-01T19:00:00-05:00","dateModified":"2021-12-02T15:17:05-05:00"},{"@type":"WebSite","@id":"https:\/\/z3news.com\/w\/#website","url":"https:\/\/z3news.com\/w\/","name":"Z3 News","description":"Revealing Mystery 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18:40:48","updated":"2025-07-16 13:51:56","seo_analyzer_scan_date":null,"focus_keyword":null,"additional_keywords":null,"truseo_locale":null},"aioseo_breadcrumb":"<div class=\"aioseo-breadcrumbs\"><span class=\"aioseo-breadcrumb\">\n\t\t\t<a href=\"https:\/\/z3news.com\/w\/\" title=\"Home\">Home<\/a>\n\t\t<\/span><span class=\"aioseo-breadcrumb-separator\">\u00bb<\/span><span class=\"aioseo-breadcrumb\">\n\t\t\t<a href=\"https:\/\/z3news.com\/w\/category\/news\/\" title=\"News\">News<\/a>\n\t\t<\/span><span class=\"aioseo-breadcrumb-separator\">\u00bb<\/span><span class=\"aioseo-breadcrumb\">\n\t\t\t<a href=\"https:\/\/z3news.com\/w\/category\/news\/jesuit-led-organizations\/\" title=\"Jesuit Controlled Organizations\">Jesuit Controlled Organizations<\/a>\n\t\t<\/span><span class=\"aioseo-breadcrumb-separator\">\u00bb<\/span><span class=\"aioseo-breadcrumb\">\n\t\t\t<a href=\"https:\/\/z3news.com\/w\/category\/news\/jesuit-led-organizations\/fda\/\" title=\"FDA\">FDA<\/a>\n\t\t<\/span><span class=\"aioseo-breadcrumb-separator\">\u00bb<\/span><span class=\"aioseo-breadcrumb\">\n\t\t\tFDA Wants 55 Years to Release COVID Jab Reaction Data\n\t\t<\/span><\/div>","aioseo_breadcrumb_json":[{"label":"Home","link":"https:\/\/z3news.com\/w\/"},{"label":"News","link":"https:\/\/z3news.com\/w\/category\/news\/"},{"label":"Jesuit Controlled Organizations","link":"https:\/\/z3news.com\/w\/category\/news\/jesuit-led-organizations\/"},{"label":"FDA","link":"https:\/\/z3news.com\/w\/category\/news\/jesuit-led-organizations\/fda\/"},{"label":"FDA Wants 55 Years to Release COVID Jab Reaction Data","link":"https:\/\/z3news.com\/w\/fda-wants-55-years-to-release-covid-jab-reaction-data\/"}],"authors":[{"term_id":657,"user_id":687,"is_guest":0,"slug":"mercola","display_name":"Dr Joseph 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