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Npra.gov.my vaccine search - NPRA says 22 out of 45 deaths involving recipients of Covid booster dose not related to adverse effects following immunisation


NPRA says 22 out of 45 deaths involving recipients of Covid booster dose not related to adverse effects following immunisation






She said this followed claims that there were doctors who were reluctant to confirm that patients who sought follow-up treatment after the Covid-19 vaccine had AEFI-related.




NPRA says 22 out of 45 deaths involving recipients of Covid booster dose not related to adverse effects following immunisation


In another development, Head of the Pharmacovigilance Section, NPRA Compliance and Quality Control Centre, Dr Azuana Ramli said individuals with AEFI of Covid-19 vaccine could lodge a report themselves to the NPRA without waiting for confirmation from a doctor.



Of the total reports, NPRA received 1,275 AEFI reports involving booster dose, with 90 cases or 7.



Dr Roshayati said a total of 94 AEFI reports involving vaccine recipients aged between five and 11-years-old were received as of February 25, with only two reports categorised as serious She said the two serious cases involved a five-year-old girl with severe asthma symptoms who was admitted to a hospital for two days for treatment, and a 10-year-old boy who suffered from facial paralysis, but is recovering..




NPRA says 22 out of 45 deaths involving recipients of Covid booster dose not related to adverse effects following immunisation









Description: Dr Roshayati said a total of 94 AEFI reports involving vaccine recipients aged between five and 11-years-old were received as of February 25, with only two reports categorised as serious She said the two serious cases involved a five-year-old girl with severe asthma symptoms who was admitted to a hospital for two days for treatment, and a 10-year-old boy who suffered from facial paralysis, but is recovering.

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Recipients of the Covid-19 vaccine who experience adverse effects can report the AEFI through the MySejahtera application and online by filling in the Consumer Side Effect Reporting Form ConSERF through the NPRA website.
Of the total reports, NPRA received 1,275 AEFI reports involving booster dose, with 90 cases or 7.
In another development, Head of the Pharmacovigilance Section, NPRA Compliance and Quality Control Centre, Dr Azuana Ramli said individuals with AEFI of Covid-19 vaccine could lodge a report themselves to the NPRA without waiting for confirmation from a doctor.

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    +86reps
    Here are a few examples of how you can use the search feature:. npra@npra.gov.my; Phone: +603-7883 5400; Fax: +603-7956 2924, +603-7956 7075. Vaccine Lot.
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    Email: npra@npra.gov.my; Phone: +603-7883 5400; Fax: +603-7956 2924, +603-7956 7075; Drug Control Authority (DCA) DCA Members;. Search for Vaccine Lot Release.
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    During marketing of CoronaVac in Malaysia, NPRA will monitor its use to ensure effectiveness and safety. Please inform your healthcare providers or report any side effects to the National Centre for Adverse Drug Reaction Monitoring by visiting the website npra.gov.my [Consumers > Reporting Side Effects to Medicines (ConSERF) or Vaccines (AEFI)].
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    NPRA according to the timeline given. Apart from that, the PRH is required to monitor the safety profile of the registered vaccine and inform NPRA soonest possible of any untoward events. The PRH is also required to conduct all activities planned under the Risk Management Plan (RMP) as well as submit a Monthly Safety Summary Report to NPRA.
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