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First Data from Pfizer Vaccine Studies Come to Light: Experts Call Adverse Effects “Alarming”

Many experts are warning about the data that has been released regarding the results of the Pfizer vaccine trial. Among them, Aaron Kheriaty, one of the complainants on behalf of the University of California who has gone to court together with dozens of experts from around the world, to demand that the FDA release all documents related to Pfizer’s vaccine against COVID-19.

Days ago Robert Malone, one of the researchers who developed RNA as a medicine and reference expert, warned about these data.

In the lawsuit, the complainants asked the FDA to make public all the information about the pharmaceutical company, as established in the regulations, which indicate a maximum period of 20 business days in drugs like this (although it can be extended if the specific situation requires it ). The FDA responded that the number of documents was so large that it would take about 55 years to make them public, since they have a small team of personnel who should review them before they are released. The judge who is hearing this matter will decide on these dates the schedule for the documentation to be published. But for their part, the group of complainant scientists has requested that the same number of days be established (just over one hundred) that were necessary for the FDA to authorize the administration of this preparation to the population as a matter of urgency. The FDA’s response has been even more surprising, clarifying that it will take not 55 years, but 75 to have all the information accessible.

Meanwhile, Trials data have started to be published carried out in the first months in which the vaccine was applied to the population.

Aaron Kheriaty has shared the link where these documents can be accessed and highlighted some issues of interest: “The data from the first bolus of the Pfizer vaccine, following our request to the FOIA, show alarming adverse effect results:” Overall, up to February 28, 2021 (less than three months), a total of 42,086 case reports (25,379 medically confirmed and 16,707 medically unconfirmed) containing 158..893 events.


In this thread published by the expert, he details the breakdown of adverse events (three months after the start of application of the vaccine)

The published document can be consulted in full here.

The Catalan drug and pharmacy service also recognized “a large volume of known adverse effects reported” in February 2021

Information related to the month of February 2021, which fits with that from agencies, such as the Generalitat of Catalonia pointed out in this information:

The Covid-19 Vaccine and Yellow Card Program then explained what kind of issues needed to be notified.

“Given the large volume of known adverse effects reported towards COVID-19 vaccines through the Yellow Card program, and to facilitate the identification of new safety problems with COVID-19 vaccines, We ask that from now on you only notify us of the following adverse effects:

  • Unknown and / or serious, especially if they motivate a hospital admission, endanger life or have a fatal outcome
  • Adverse events of special interest (1): anaphylaxis, arrhythmia, heart failure, stress cardiomyopathy, coronary artery disease, myocarditis, sudden death or death from any cause, Guillain-Barré syndrome, disseminated encephalomyelitis, meningo de Bello, cutaneous vasculitis, erythema multiforme, microangiopathy, coagulation disorders (thromboembolism and hemorrhage), idiopathic thrombocytopenia, aseptic arthritis, aseptic arthritis, immunization), anosmia and ageusia and damage.

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