Pfizer hired 600 full-time employees to handle the volume of reported adverse events resulting from its mRNA vaccines, lawsuit filing shows | tech news

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It has been a while since we last reported on the Covid pandemic. At a time when we are all trying to move on and put the pandemic behind us, a new Omicron subvariant has reportedly been discovered in the UK.

The virus, known as variant XE, has been detected in 637 patients in the UK so far, according to the latest data from the UK Health Security Agency. The organization said there is currently insufficient data to draw any conclusions about the transmissibility or severity of the variant.

Meanwhile, there’s a new revelation about why the Food and Drug Administration (FDA) has been trying to hide information about Pfizer’s mRNA vaccines for 55 years. As we reported late last year, on November 15, the FDA asked a federal judge to fully release by the year 2076 all data and documents the agency used as the basis for approving and licensing Pfizer-BioNTech’s Covid19 vaccine. Now we know why.

According to a new report from The Informed Consent Action Network (ICAN), a nonprofit organization focused on the scientific integrity of vaccines and the pharmaceutical industry, Pfizer hired 600 full-time employees to handle the volume of reported adverse events from its mRNA vaccines in the last two years.

The attorneys representing ICAN are representing the plaintiff in a lawsuit against the FDA to obtain Pfizer’s Covid vaccine documents. You recently secured an unedited copy of a previously prepared post-marketing adverse event report. The overturned redactions show that within weeks of administering Pfizer’s vaccine under the emergency authorization, Pfizer appeared to unexpectedly have to hire 600 full-time employees “to help mitigate the large increase in adverse event reports” the company is receiving.

You can find the original redacted copy of the report here and the unedited copy here, with redactions removed on page 6.

The removed redactions also show the number of doses shipped at the date of the report (just over 126 million doses) and at least provide a common denominator to help understand the volume of post-vaccination reports. Specifically, this is the number of doses shipped and the report does not reflect the number of doses administered up to the date of the report.

Below is a redacted version of the legal document.

CENSORED-5.3.6 postmarketing experience

Below is an unedited version of the legal document.



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