DISCLAIMER: This page is intended for members of the general public in Luxembourg only.
The information provided on this site is intended for general information and education for Luxembourg-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 NuvaxovidTM JN.1 dispersion for injection COVID-19 Vaccine (recombinant, adjuvanted)
NuvaxovidTM JN.1 dispersion for injection COVID-19 Vaccine (recombinant, adjuvanted) has been granted full approval by the European Commission for active immunisation to prevent COVID-19 caused by SARS-CoV-2 in individuals 12 years of age and older.
Important information
For more information about the NuvaxovidTM JN.1 dispersion for injection COVID-19 Vaccine (recombinant, adjuvanted), download the Package Leaflet.
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.
Either you or your healthcare professional can report any suspected adverse reactions via the national reporting system of Luxembourg.
Centre Régional de Pharmacovigilance de Nancy
Bâtiment de Biologie Moléculaire et de Biopathologie (BBB)
CHRU de Nancy – Hôpitaux de Brabois
Rue du Morvan
54 511 VANDOEUVRE LES NANCY CEDEX
Tél: (+33) 3 83 65 60 85 / 87
e-mail: [email protected]
or
Direction de la Santé
Division de la Pharmacie et des Médicaments
20, rue de Bitbourg
L-1273 Luxembourg-Hamm
Tél.: (+352) 2478 5592
e-mail: [email protected]
Link to the notification form: www.guichet.public.lu/fr/entreprises/sectoriel/sante/medecins/notification-effets-indesirables-medicaments.html
Contact Us
Tel: +352 20 33 17 08
09:00 - 17:00
Monday - Friday