The Malta Independent 15 May 2024, Wednesday
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Updated: Malta received AstraZeneca batch suspended by six countries over blood clot fears

Thursday, 11 March 2021, 11:52 Last update: about 4 years ago

Malta is one of 17 EU countries to receive a batch of AstraZeneca vaccines which six countries have suspended from use after a person died of multiple thrombosis some days after receiving a dose of the vaccine.

One person died of multiple thrombosis – formation of blood clots within blood vessels – 10 days after their vaccine, the European Medicines Agency (EMA) said.

A second patient was diagnosed with pulmonary embolism – where blockages form in the arteries in the lungs – but is now recovering.

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As of Tuesday this week, two other clotting conditions had been identified in patients that had received a dose from the same batch.

A European Medicines Agency statement confirmed that Malta had received doses from the aforementioned batch of vaccines.  Questions sent to the Health Ministry on whether it will be suspended until investigations take place are yet to be answered.

The EMA said there is currently no evidence that the vaccine caused the conditions, and that thrombosis is not listed as a potential side effect of the vaccine.

It said that the batch labelled ABV5300 comprised one million doses and had been delivered to 17 EU countries.

Austria, Denmark, Estonia, Lithuania, Luxembourg, and Latvia have now suspended its use to allow time for the EMA’s Pharmacovigilance Risk Assessment Committee (PRAC) to conduct an investigation.

The EMA said: “Although a quality defect is considered unlikely at this stage, the batch quality is being investigated.”

It said PRAC were investigating the thrombosis conditions linked to the same batch as well as all other reports of thrombosis and related blood clotting conditions reported post-vaccination.

“The information available so far indicates that the number of thromboembolic events in vaccinated people is no higher than that seen in the general population,” it said.

The EMA said as of Tuesday, there had been 22 reports of such conditions among the three million people to receive the AstraZeneca jab in the European Economic Area.

It said further information would be released as the investigation progresses.

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