Pfizer had applied for and was given a 55 year moratorium on releasing ANY data in relation to the experimental drug program implemented worldwide we now commonly and mistakenly call ‘the vaccine’. A recent court case in America saw this overturned. Pfizer, one of the most fined companies in the world for its products, policies and integrity, was ordered to release documents. Despite being able to produce over 350,000 documents in 105 days when seeking Government approval for its new mRNA therapy, Pfizer stated it was only able to release 500 documents a month. This was accepted by the courts and allowed Pfizer to effectively cherry-pick what documents it could release. The first 500 were recently released. Remember these are only 500 of all the available documents. Given the track record of Pfizer, one would assume these 500 are some of the least offensive documents. 500 documents that apparently were never previously available to Governments when they were making decisions concerning the approval of Pfizer’s mRNA drugs. 500 documents with concerns and information that may have made huge differences in who took up the offer to be a part of this worldwide experiment.
One of the documents released by Pfizer reveals a vast array of previously unknown adverse events compiled from official sources around the world. Pfizer’s initial fact sheet provided to hospitals contained 21 potential adverse reactions as a result of vaccination. All of these were considered minor requiring little or no treatment. The exception is the severe allergic reactions, myocarditis and pericarditis (inflammation of the heart). With the release of this document Pfizer now concedes there are over 100 diseases associated with its ‘vaccination’. They knew this BEFORE they issued the fact sheets. They knew this before they spoke to the various governments around the world stating their ‘vaccines’ were totally safe. They knew this while telling the world their ‘vaccines’ were safe. Now they graciously concede that this jump from 21 potential adverse events to 100+ is a ‘large increase’ in adverse event types. They also have conceded that there is a large increase in adverse event reports and that even this huge volume is underreported. Far from being minor reactions that require ‘panadol and rest’ or even worse being passed off as ‘psychosomatic’ or ‘due to anxiety, these newly listed adverse event types pose long term and serious health risks. There is a very real possibility that large numbers of those taking this experimental drug will suffer long term and permanent injuries.
Questions need to be asked.
Was our government informed of these potential adverse reactions? If they were, why did they go ahead with the rollout? If they were not informed but are now aware they were lied to or at least had crucial information withheld why are they not suspending the rollout? Why are they not running a better information campaign so its citizens can truly make an informed decision? Money? Who has benefited from this? Control? Our various premiers have used this false information to bring in policies that under normal circumstances would not even be thought appropriate or necessary. These are the first documents released by Pfizer. The ones that were to remain secret for 55 years. One would assume these are not the worst but the best of the worst and if these are the best of the worst then this country should be up in arms. At best we’ve been misinformed by a government deceived by a large drug company that has a track record of manipulating data to suit its purposes. If this is the case then our government should stand down immediately for its incompetence. For signing away billions of dollars of taxpayers money on a fraud. At worst our government has been complicit in a rollout of a drug with known long-lasting and extremely dangerous side effects.https://afipn.com.au/pfizer-documents-reveal-over-100-adverse-reactions-associated-with-the-vaccine/https://archive.md/cUooh