The FDA shared the first batch of documents linked to the Pfizer C-19 vaccine after a federal judge ordered that they comply with a massive FOIA request filed by a government accountability group called Public Health and Medical Professionals for Transparency.
The group of more than 30 experts asked the federal government to share data that factored into the agency’s hasty decision to grant Pfizer’s vaccine EUA. In a shameless effort to hide data, the FDA challenged the FOIA request in court. Once the agency was told that it must turn over the documents, Justice Department lawyers representing the FDA wanted the judge to allow them an unthinkable 55 years to process the request, stating that it can release only 500 pages a month.
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One motion filed by the same group of doctors is pending in federal court that would force the FDA to expedite processing and release these data.
The FDA must comply with the original order to begin turning over documents.
Official Pfizer document called Cumulative Analysis of Post-Authorization Adverse Event Records Reports, in the first three months of the vaccine’s roll out under the FDA’s EUA from December first, 2020, until February twenty-eighth, 2021, shows tens of thousands of side effects and 1200 deaths.
The report included side effects from the vaccine that the experts regarded as severe, and thousands more submissions were left out of this data.
There were 42,086 case reports of people who had side effects; 13,739 came from the US and 13 404 from the UK.
“Due to the large numbers of spontaneous adverse event reports received for the product, the MAH has prioritised the processing of serious cases, in order to meet expedited regulatory reporting timelines and ensure these reports are available for signal detection and evaluation activity.
Non-serious cases are processed as soon as possible and no later than 90 days from receipt. Pfizer has also taken a multiple actions to help alleviate the large increase of adverse event reports.”
The FDA didn’t immediately pull the vaccine out of reach? The document clearly shares that the data includes recorded adverse events, which is only a portion of the true number of side effects that happened.
“Reports are submitted voluntarily, and the magnitude of underreporting is unknown.
Some of the factors that may influence whether an event is reported include: length of time since marketing, market share of the drug, publicity about a drug or an AE, seriousness of the reaction, regulatory actions, awareness by health professionals and consumers of adverse drug event reporting, and litigation.”
‘’ Yet somehow the paper concludes that the “review of available data” was good enough and demonstrated a “favorable benefit-risk balance” for the rushed vaccine.
What’s the benefit-risk balance on a virus that has a 99.9% recovery rate? The benefit – at least for Pfizer – is clear; It doesn’t matter how many otherwise healthy lives are lost – they are CASHING into the tune of $1,000 PER SECOND with a projected $36 BILLION in profit this year from the vaccine alone – it’s criminal.’’ The document stated.
Here you will find the entire document.