https://yourlocalepidemiologist.subs...ds-fda-meeting
Es gab 5 Vorfälle bei dieser Anzahl an Teilnehmern:
Zitat:
2,268 trial participants (including 1,518 vaccine recipients) followed for at least two months past the 2nd dose
A “safety expansion” group of an additional 2,379 participants (1,500 vaccine recipients) followed for a median of 2.4 weeks after the second dose. This was done per the FDAs request “to allow for more robust assessment of serious adverse events and other adverse events of interest”.
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Und zwar. Trommelwirbel:
Zitat:
There were 5 severe adverse events. None were linked to the vaccine:
Ingestion of a penny (1 person in the vaccine group)
Fractures (2 people in the vaccine group and 1 in the placebo)
Infective arthritis (one person in vaccine group)
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Ja die Anzahl ist nicht hoch genug um die ultra seltenen potentiellen Nebenwirkungen zu haben, aber ein weiterer Schritt hin zu einer zugelassenen Impfung für Kinder.