As
part of a regular review of safety reports for the vaccine,
Vaxzevria, the European Medicines Agency's safety committee is
analysing data provided on cases of Guillain-Barre syndrome, the
regulator said.
AstraZeneca did not immediately respond to requests for comment.
(Reporting by Pushkala Aripaka in Bengaluru and Ludwig Burger in
Frankfurt; Editing by Shinjini Ganguli)
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