DISCLAIMER: This page is intended for members of the general public in United Kingdom - Great Britain only.
The information provided on this site is intended for general information and education for United Kingdom - Great Britain-based members of the public and is not intended to be a substitute for the advice provided by a physician or other qualified Healthcare Professional.
Information about the Nuvaxovid dispersion for injection COVID-19 Vaccine (recombinant, adjuvanted)
This medicinal product has been given conditional marketing authorisation for Great Britain by the Medicines and Healthcare products Regulatory Agency (MHRA). This conditional marketing authorisation allows Nuvaxovid to be used for active immunisation to prevent COVID-19 caused by SARS-CoV-2 in individuals aged 12 years of age and older.
If you have any questions or concerns regarding Nuvaxovid dispersion for injection COVID-19 Vaccine (recombinant, adjuvanted), please speak to your doctor, nurse or Healthcare Professional.
Important information
For more information about the Nuvaxovid dispersion for injection COVID-19 Vaccine (recombinant, adjuvanted), view the PDF file of the Product Information Leaflet.
Report a Side Effect
If you get any side effects, talk to your doctor, pharmacist, or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Coronavirus Yellow Card reporting site https://coronavirus-yellowcard.mhra.gov.uk/ or search for MHRA Yellow Card in the Google Play or Apple App Store, and include the vaccine brand and batch/lot number, if available. By reporting side effects, you can help provide more information on the safety of this vaccine.
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