Novavax Medical Information
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Information about the NuvaxovidTM COVID-19 Vaccine (recombinant, adjuvanted) (also known as NVX-CoV2373)
This medicinal product has been given conditional marketing authorisation in Northern Ireland by the European Medicines Agency (EMA). NuvaxovidTM COVID-19 Vaccine (recombinant, adjuvanted) has been granted a conditional marketing authorisation for active immunisation to prevent COVID-19 caused by SARS-CoV-2 in individuals 18 years of age and older.
If you have any questions or concerns regarding the NuvaxovidTM COVID-19 Vaccine (recombinant, adjuvanted), please speak to your doctor, nurse or Healthcare Professional.
Important information
For more information about the NuvaxovidTM COVID-19 Vaccine (recombinant, adjuvanted), view the PDF file of the Package Leaflet.
Package Leaflet (PL)
Request Medical Information
Novavax is unable to provide medical advice regarding your health condition. Please consult your doctor, nurse or other healthcare provider, who is in the best position to advise you about the suitability of a particular treatment as they have access to the details of your medical history, as well as information on all medicinal products.
To ask Novavax Medical Information a question about a Novavax product please call
+44 203 514 1838 between 09:00 - 17:00.
Report a Side Effect
If you are concerned about a side effect, it can be reported directly via the Coronavirus Yellow Card reporting site https://coronavirus-yellowcard.mhra.gov.uk/ or search for MHRA Yellow Card on the Google Play or Apple Store. When completing a report, please include the vaccine brand and batch/Lot number if available.
Report a Product Quality Complaint
If you have a product quality complaint related to a physical issue with a Novavax product or its packaging, please report the complaint via ONE of the following ways:
Option 1: Complete and submit a Product Quality Complaint Form by clicking on the button below.
Report a Product Quality Complaint
Option 2: Call +44 203 514 1838 between 09:00 - 17:00.