ATAGI statement in response to European decisions about AstraZeneca vaccine

ATAGI statement news item

AstraZeneca clinical update

ATAGI notes the suspension of the AstraZeneca vaccine program in several European countries due to reports of a potential link with thrombotic (clotting) events. Based on evidence to date, ATAGI do not see any reason to pause use of the AstraZeneca vaccine in Australia.

Thrombotic events occur commonly in the absence of vaccination. It is noted that the rates of thrombotic events are not higher in vaccine recipients than the expected background rate. The MHRA have stated that no signals have been identified in the UK where more than 11 million doses have been administered to date.

The TGA is closely monitoring the situation and has been in communication with regulators including the EMA and the MHRA. Further clinical details of the cases are being reviewed by the EMA with further information expected this week.

No cases of coagulation disorders have been identified following COVID vaccination in Australia. Clotting disorders are designated as 'adverse events of special interest' that are closely monitored.

ATAGI encourages healthcare providers and the public to report any unexpected or serious adverse events, including thrombotic disorders, occurring following any COVID-19 vaccines.

/Media Release. This material from the originating organization/author(s) might be of the point-in-time nature, and edited for clarity, style and length. Mirage.News does not take institutional positions or sides, and all views, positions, and conclusions expressed herein are solely those of the author(s).View in full here.