FDA Releases More Data On “Adverse Reactions” To Big Pharma product

FDA Releases More Data On “Adverse Reactions” To Big Pharma product
The Liberty Beacon / This article was posted by TLB Staff

FDA Releases More Data On “Adverse Reactions” To Pfizer Vaccine


As the FDA prepares to approve Pfizer’s new pill for treating high-risk patients infected with COVID, more information about dangerous side effects tied to its vaccine are coming to light.

Just yesterday, we reported another death tied to the vaccine in New Zealand. Now, documents released by the FDA reveal that drugmaker Pfizer recorded nearly 160K adverse reactions to its COVID vaccine in the initial months of its rollout.

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The data were obtained by a group of doctors, professors, and journalists calling themselves Public Health and Medical Professionals for Transparency. They filed a Freedom of Information Act request with the FDA asking for their release. And the first tranche of documents revealed that, as of February 2021, when Pfizer’s shot was being rolled out worldwide on an emergency basis, the drugmaker had compiled more than 42K case reports detailing nearly 160K individual adverse reactions to the vaccine.

The data show the bulk of the adverse event cases, both serious and non-serious, were classified as “general disorders”.

<p><img loading=”lazy” class=”inline-images image-style-inline-images aligncenter” src=”https://i0.wp.com/assets.zerohedge.com/s3fs-public/styles/inline_image_mobile/public/inline-images/pfizer10.jpg?resize=660%2C525&amp;ssl=1″ alt width=”660″ height=”525″ data-entity-type=”file” data-entity-uuid=”bb8a3624-503f-4784-a5ff-515539325a4a” data-responsive-image-style=”inline_images” data-recalc-dims=”1″></p>

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