COVID-19 Vaccine (inactivated, adjuvanted) Valneva

RSS

Withdrawn

This medicine's authorisation has been withdrawn

COVID-19 vaccine (inactivated, adjuvanted, adsorbed)
MedicineHumanWithdrawn

Lithuanian is available via eTranslation, the European Commission's machine translation service.

Translate to Lithuanian | Important information about machine translation

  • Rolling review
  • Application under evaluation
  • CHMP opinion
  • European Commission decision

Overview

On 12 October 2023, the European Commission withdrew the marketing authorisation for COVID-19 Vaccine (inactivated, adjuvanted) Valneva (SARS-CoV-2 virus, strain Wuhan hCoV-19/Italy/INMI1- isl/2020, inactivated) in the European Union (EU). The withdrawal was at the request of the marketing authorisation holder, Valneva Austria GmbH, which notified the European Commission of its decision to permanently discontinue the marketing of the product for commercial reasons. 

COVID-19 Vaccine (inactivated, adjuvanted) Valneva was granted marketing authorisation in the EU on 24 June 2022 for active immunisation against coronavirus disease 2019 (COVID-19). The marketing authorisation was initially valid for a 5-year period. 

The European Public Assessment Report (EPAR) for COVID-19 Vaccine (inactivated, adjuvanted) Valneva is updated to indicate that the marketing authorisation is no longer valid.

български (BG) (412.12 KB - PDF)

Rodyti

español (ES) (296.05 KB - PDF)

Rodyti

čeština (CS) (353.49 KB - PDF)

Rodyti

dansk (DA) (280.97 KB - PDF)

Rodyti

Deutsch (DE) (314.28 KB - PDF)

Rodyti

eesti (ET) (273.24 KB - PDF)

Rodyti

ελληνικά (EL) (416.76 KB - PDF)

Rodyti

français (FR) (301.09 KB - PDF)

Rodyti

hrvatski (HR) (340.66 KB - PDF)

Rodyti

italiano (IT) (285.18 KB - PDF)

Rodyti

latviešu (LV) (359.53 KB - PDF)

Rodyti

lietuvių (LT) (343.51 KB - PDF)

Rodyti

magyar (HU) (327.46 KB - PDF)

Rodyti

Malti (MT) (397.24 KB - PDF)

Rodyti

Nederlands (NL) (302.98 KB - PDF)

Rodyti

polski (PL) (353.81 KB - PDF)

Rodyti

português (PT) (293.01 KB - PDF)

Rodyti

română (RO) (360.97 KB - PDF)

Rodyti

slovenčina (SK) (371.58 KB - PDF)

Rodyti

slovenščina (SL) (329.43 KB - PDF)

Rodyti

suomi (FI) (277.49 KB - PDF)

Rodyti

svenska (SV) (281.18 KB - PDF)

Rodyti

Product information

български (BG) (1.39 MB - PDF)

Rodyti

español (ES) (1.1 MB - PDF)

Rodyti

čeština (CS) (1.19 MB - PDF)

Rodyti

dansk (DA) (1.01 MB - PDF)

Rodyti

Deutsch (DE) (1.08 MB - PDF)

Rodyti

eesti (ET) (974.37 KB - PDF)

Rodyti

ελληνικά (EL) (1.46 MB - PDF)

Rodyti

français (FR) (1.04 MB - PDF)

Rodyti

hrvatski (HR) (1.15 MB - PDF)

Rodyti

italiano (IT) (1.09 MB - PDF)

Rodyti

latviešu (LV) (1.27 MB - PDF)

Rodyti

lietuvių (LT) (1.23 MB - PDF)

Rodyti

magyar (HU) (1.2 MB - PDF)

Rodyti

Nederlands (NL) (1.08 MB - PDF)

Rodyti

polski (PL) (1.27 MB - PDF)

Rodyti

português (PT) (1.02 MB - PDF)

Rodyti

română (RO) (1.3 MB - PDF)

Rodyti

slovenčina (SK) (1.21 MB - PDF)

Rodyti

slovenščina (SL) (1.18 MB - PDF)

Rodyti

suomi (FI) (1.03 MB - PDF)

Rodyti

svenska (SV) (982.29 KB - PDF)

Rodyti

norsk (NO) (991.74 KB - PDF)

Rodyti
Latest procedure affecting product information:II/0004
12/10/2023
icon globe

This medicine’s product information is available in all official EU languages.
Select 'available languages' to access the language you need.

 

Product information documents contain:

  • summary of product characteristics (annex I);
  • manufacturing authorisation holder responsible for batch release (annex IIA);
  • conditions of the marketing authorisation (annex IIB);
  • labelling (annex IIIA);
  • package leaflet (annex IIIB).

български (BG) (144.11 KB - PDF)

Rodyti

español (ES) (121.79 KB - PDF)

Rodyti

čeština (CS) (126.11 KB - PDF)

Rodyti

dansk (DA) (119.05 KB - PDF)

Rodyti

Deutsch (DE) (123.25 KB - PDF)

Rodyti

eesti (ET) (116.88 KB - PDF)

Rodyti

ελληνικά (EL) (134.61 KB - PDF)

Rodyti

français (FR) (124.6 KB - PDF)

Rodyti

hrvatski (HR) (122.34 KB - PDF)

Rodyti

italiano (IT) (120.11 KB - PDF)

Rodyti

latviešu (LV) (123.85 KB - PDF)

Rodyti

lietuvių (LT) (123.75 KB - PDF)

Rodyti

magyar (HU) (121.79 KB - PDF)

Rodyti

Malti (MT) (134.68 KB - PDF)

Rodyti

Nederlands (NL) (120.28 KB - PDF)

Rodyti

polski (PL) (137.11 KB - PDF)

Rodyti

português (PT) (124.04 KB - PDF)

Rodyti

română (RO) (123.01 KB - PDF)

Rodyti

slovenčina (SK) (125.73 KB - PDF)

Rodyti

slovenščina (SL) (124.15 KB - PDF)

Rodyti

suomi (FI) (114.96 KB - PDF)

Rodyti

svenska (SV) (117.48 KB - PDF)

Rodyti

Íslenska (IS) (131.46 KB - PDF)

Rodyti

norsk (NO) (129.29 KB - PDF)

Rodyti

Product details

Name of medicine
COVID-19 Vaccine (inactivated, adjuvanted) Valneva
Active substance
COVID-19 vaccine (inactivated, adjuvanted, adsorbed)
International non-proprietary name (INN) or common name
COVID-19 vaccine (inactivated, adjuvanted, adsorbed)
Therapeutic area (MeSH)
COVID-19 virus infection
Anatomical therapeutic chemical (ATC) code
J07BX03

Pharmacotherapeutic group

Vaccines

Therapeutic indication

COVID-19 Vaccine (inactivated, adjuvanted) Valneva is indicated for active immunisation to prevent COVID-19 caused by SARS-CoV-2 in individuals 18 to 50 years of age. 

The use of this vaccine should be in accordance with official recommendations.

Authorisation details

EMA product number
EMEA/H/C/006019
Marketing authorisation holder
Valneva Austria GmbH

Campus Vienna Biocenter 3
Landstrasse
A-1030 Vienna
Austria

Opinion adopted
23/06/2022
Marketing authorisation issued
24/06/2022
Withdrawal of marketing authorisation
12/10/2023
Revision
6

Assessment history

Safety updates

This page was last updated on

Share this page