AstraZeneca's COVID-19 vaccine trial in the United States is expected to resume as early as this week after the US Food and Drug Administration completed its review of a serious illness, four sources told Reuters., after a participant in the company's British trial fell ill with what was suspected to be a rare spinal inflammatory disorder called transverse myelitis.
He said the AstraZeneca/Oxford and University of Queensland projects used different approaches, with UQ's being a more "classical" vaccine model while AstraZeneca's was a newer approach, and it was a positive that both projects could be made in Melbourne. “In this case, after considering the information, the independent reviewers and MHRA recommended that vaccinations should continue,” the draft consent form stated. “Close monitoring of the affected individual and other participants will be continued.”
A J&J spokesman on Tuesday said the study remains on pause as the company continues its review of medical information before deciding to restart the trial. J&J noted that its "study pause" was voluntary, in contrast to AstraZeneca's "regulatory hold," which is imposed by health authorities. FDA "has come to the same conclusion as the other drug regulators including the MHRA," the letter states.The Health Research Authority, which helps regulate UK medical research, did not say if the letter had been sent or respond to questions about it.
As a nurse vaccinator I would never give a needle like that. Where do these photos come from ?
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