Malaysia

M’sia to review AstraZeneca vaccine before roll-out: Khairy

We still have time to decide as batch only scheduled for May, says coordinating minister

Updated 5 years ago · Published on 08 Apr 2021 1:00PM

M’sia to review AstraZeneca vaccine before roll-out: Khairy
National Covid-19 Immunisation Programme Coordinating Minister Khairy Jamaluddin says safety is paramount when it comes to vaccines. – Information Dept pic, April 8, 2021

KUALA LUMPUR – Malaysia will review the use of the AstraZeneca Covid-19 vaccine in the country following the European Medicines Agency’s (EMA) findings that unusual blood clots with low blood platelets should be listed as very rare side effects of the vaccine.

National Covid-19 Immunisation Programme Coordinating Minister Khairy Jamaluddin said the Covid-19 Vaccine Supply Access Guarantee Special Committee (JKJAV) will deliberate on the matter.

“We take note of EMA’s announcement on the AstraZeneca vaccine. JKJAV will deliberate on the matter and decide if we will go ahead with using AZ (AstraZeneca) in our portfolio of vaccines. Safety is paramount,” he said in a tweet today.

Yesterday, Khairy had said that Malaysia still has time to decide on AstraZeneca vaccine as it was only coming from the Covax facility in May.

The EMA’s safety committee (PRAC) yesterday shared its conclusion on the review of AstraZeneca and confirmed that the benefits of the vaccine in preventing Covid-19 overall outweigh the risks of side effects.

The European Union agency reminded healthcare professionals and people receiving the vaccine to remain aware of the possibility of very rare cases of blood clots combined with low levels of blood platelets occurring within two weeks of vaccination.

“So far, most of the cases reported have occurred in women under 60 years of age within two weeks of vaccination. Based on the currently available evidence, specific risk factors have not been confirmed,” it said in a statement posted on its website.

The committee said it had reviewed 62 cases of cerebral venous sinus thrombosis and 24 cases of splanchnic vein thrombosis reported in the EU drug safety database as of March 22, in which 25 million individuals had received the vaccine, of which 18 were fatal.

The PRAC also took into consideration all currently available evidence, including the advice from an ad hoc expert group. – Bernama, April 8, 2021

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