(Adds background)
March 10 (Reuters) - The European Medicines Agency said on
Wednesday there was no evidence so far linking AstraZeneca's
COVID-19 vaccine to illnesses in two people who received
it in Austria, one of whom died 10 days after being inoculated.
The Austrian national health authority suspended the use of
a batch of the vaccine after a person who was vaccinated was
diagnosed with multiple thrombosis and later died, and another
was hospitalised with pulmonary embolism.
"There is currently no indication that vaccination has
caused these conditions, which are not listed as side effects
with this vaccine," the EMA said in its statement. (https://bit.ly/3l1A0n0)
"Although a quality defect is considered unlikely at this
stage, the batch quality is being investigated."
Austria said on Sunday it was suspending inoculations with
the batch as a precaution. The batch was sent to 17 EU countries
in total and comprised 1 million doses of the AstraZeneca
vaccine.
The Anglo-Swedish company has said all batches are subject
to strict and rigorous quality controls and that there have been
"no confirmed serious adverse events associated with the
vaccine". It said it was in contact with Austrian authorities
and would fully support the investigation.
The EU regulator said the number of thromboembolic events -
marked by the formation of blood clots in the body - in people
who have received the AstraZeneca vaccine is no higher than that
seen in the general population, with 22 cases of such events
being reported among the 3 million people who have received it
as of March 9.
The EU approved AstraZeneca's shot at the end of January,
saying it was effective and safe to use, while the World Health
Organization listed it for emergency use in mid-February.
Adverse reactions seen in trials were short-lived for the
most part and blood-clotting problems were not reported.
(Reporting by Yadarisa Shabong in Bengaluru and Keith Weir in
London; Editing by Shounak Dasgupta and Paul Simao)