Thromboembolic events after Ad.26. COV2 .S COVID ‐19 vaccine: Reports to the Vaccine Adverse Event Reporting System

Author:

Woo Emily Jane1,Mba‐Jonas Adamma1,Thomas Alisha1,Baer Bethany1,Day Brendan1ORCID,Kim Yeowon1,Gomez‐Lorenzo Margarita1,Nair Narayan1

Affiliation:

1. Office of Biostatistics and Pharmacovigilance, Center for Biologics Evaluation and Research Food and Drug Administration Silver Spring Maryland USA

Publisher

Wiley

Subject

Pharmacology (medical),Epidemiology

Reference28 articles.

1. U.S. Food & Drug Administeration.Emergency use authorization letter for Janssen COVID‐19 vaccine. Accessed July 2022.https://www.fda.gov/media/146303/download

2. The Advisory Committee on Immunization Practices’ Interim Recommendation for Use of Janssen COVID-19 Vaccine — United States, February 2021

3. U.S. Food & Drug Administeration.Fact sheet for healthcare providers administering vaccine (vaccination providers). Emergency use authorization (EUA) of Janssen COVID‐19 vaccine to prevent coronavirus disease 2019 (COVID‐19). Accessed July 2022.https://www.fda.gov/media/146304/download

4. U.S. Food & Drug Administeration.FDA Briefing Document: Janssen Ad26.COV2.S Vaccine for the Prevention of COVID‐19. Accessed July 2022.https://www.fda.gov/media/146217/download

5. US Case Reports of Cerebral Venous Sinus Thrombosis With Thrombocytopenia After Ad26.COV2.S Vaccination, March 2 to April 21, 2021

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