Novavax Medical Information
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NuvaxovidTM COVID-19 Vaccine (recombinant, adjuvanted)
NuvaxovidTM COVID-19 Vaccine (recombinant, adjuvanted) has been granted full marketing authorisation by the EMA for active immunisation to prevent COVID-19 caused by SARS-CoV-2 in individuals 12 years of age and older in accordance with official recommendations. Nuvaxovid can be administered as booster dose approximately 6 months after the second dose in individuals 18 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 resources below.
Summary of Product Characteristics (SmPC)
Request Medical Information
Do you have a medical or scientific question about a Novavax medicinal product? Get in touch with Novavax Medical Information experts who will provide tailored, evidence-based, balanced, and up-to-date medical information.
Healthcare Professionals may request medical information via ONE of the following ways:
Option 1: Complete and submit a Medical Information Request Form by clicking on the button below.
Option 2: Call +351 21 020 6287 between 09:00-17:00.
Report an Adverse Event (AE)
If you are concerned about an adverse event, it should be reported to the National Authority of Medicines and Health Products, IP (INFARMED, IP) at http://www.infarmed.pt.
Alternatively, adverse events of serious concern in association with a Novavax product can be reported to Novavax Pharmacovigilance at +351 21 020 6287 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.
Report a Product Quality Complaint
Option 2: Call +351 21 020 6287 between 09:00-17:00.