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April 19, 2021 (Children’s Health Defense) — U.S. and European health officials are scrutinizing the Johnson & Johnson (J&J) and AstraZeneca COVID vaccines for possibly causing blood clots and related blood disorders in vaccine recipients.
But evidence is mounting that the Pfizer and Moderna vaccines cause similar adverse reactions — and U.S. regulatory officials were alerted to that fact as far back as December 2020.
The Centers for Disease Control and Prevention (CDC) on Wednesday convened an emergency meeting of its Advisory Committee on Immunization Practices (ACIP) to determine whether to lift a ban on the J&J vaccine. The ban was put in place Tuesday, after reports of blood clots.
During the meeting, committee members hailed the Pfizer and Moderna mRNA vaccines as great alternatives to the J&J vaccine because there were “no safety signals” — suggesting, unlike the J&J and AstraZeneca adenovirus-based vaccines, mRNA vaccines are not associated with blood clots.
On Tuesday, Peter Marks, director of the Center for Biologics Evaluation and Research at the U.S. Food and Drug Administration (FDA), said on a call with reporters there had been no reported cases of cerebral venous sinus thrombosis (CVST) with thrombocytopenia (low blood platelets that can cause dangerous internal bleeding)
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