Enhanced passive safety surveillance of high‐dose and standard‐dose quadrivalent inactivated split‐virion influenza vaccines in Germany and Finland during the influenza season 2021/22

Author:

Gandhi‐Banga Sonja1ORCID,Wague Sophie2,Shrestha Anju34,Syrkina Olga3,Talanova Oxana2,Nissilä Markku5,Stuff Karl6,Monfredo Céline7

Affiliation:

1. Sanofi Toronto ON Canada

2. Sanofi Lyon France

3. Sanofi Swiftwater Pennsylvania USA

4. Affiliation at the time of the study; current affiliation Regeneron Pharmaceuticals Basking Ridge New Jersey USA

5. Terveystalo Biobank and Clinical Research Turku Finland

6. Arztpraxis Dr. Stuff Donaueschingen Germany

7. Global Biostatistical Sciences, Sanofi Marcy l'Etoile France

Funder

Sanofi

Publisher

Wiley

Subject

Infectious Diseases,Public Health, Environmental and Occupational Health,Pulmonary and Respiratory Medicine,Epidemiology

Reference21 articles.

1. Pharmacovigilance risk assessment committee (PRAC) EMA.Interim guidance on enhanced safety surveillance for seasonal influenza vaccines in the EU 2014[cited2014April 10]; Available from:https://www.ema.europa.eu/en/documents/scientific-guideline/interim-guidance-enhanced-safety-surveillance-seasonal-influenza-vaccines-eu_en.pdf

2. Routine surveillance of adverse events following immunization as an important tool to monitor vaccine safety

3. Surveillance of adverse events following immunisation: the model of SAEFVIC, Victoria;Clothier HJ;Commun Dis Intell Q Rep,2011

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