NuvaxovidTM COVID-19 Vaccine (recombinant, adjuvanted)
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 12 years of age and older.
Information on the NuvaxovidTM COVID-19 Vaccine (recombinant, adjuvanted)
If your enquiry is regarding the NuvaxovidTM COVID-19 Vaccine (recombinant, adjuvanted), you can find some useful information in the resource below.
Request Medical Information
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Report an Adverse Event (AE)
If you are concerned about any potential side effects, talk to your doctor, pharmacist, or nurse. This includes any possible side effects not listed in the Package Leaflet.
Alternatively, adverse events of serious concern in association with a Novavax product can be reported to the Netherlands Pharmacovigilance Centre Lareb at https://www.lareb.nl/en or to Novavax Pharmacovigilance at +31 020 808 2762 or via the Novavax Adverse Event Reporting Form.
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.
Option 2: Call +31 020 808 2762 between 09:00-17:00.