Safety review of tetanus toxoid, reduced diphtheria toxoid, acellular pertussis vaccines (Tdap) in adults aged ≥65 years, Vaccine Adverse Event reporting System (VAERS), United States, September 2010–December 2018

Penina Haber; Pedro L. Moro; Carmen Ng; Graça M. Dores; Silvia Perez-Vilar; Paige L. Marquez; Maria Cano

doi:10.1016/j.vaccine.2019.11.074

Safety review of tetanus toxoid, reduced diphtheria toxoid, acellular pertussis vaccines (Tdap) in adults aged ≥65 years, Vaccine Adverse Event reporting System (VAERS), United States, September 2010–December 2018

Vaccine ◽

10.1016/j.vaccine.2019.11.074 ◽

2020 ◽

Vol 38 (6) ◽

pp. 1476-1480 ◽

Cited By ~ 1

Author(s):

Penina Haber ◽

Pedro L. Moro ◽

Carmen Ng ◽

Graça M. Dores ◽

Silvia Perez-Vilar ◽

...

Keyword(s):

United States ◽

Adverse Event ◽

Tetanus Toxoid ◽

Reporting System ◽

Adverse Event Reporting System ◽

Adverse Event Reporting ◽

Diphtheria Toxoid ◽

Event Reporting ◽

Safety Review

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Adverse events after Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis (Tdap) Vaccine administered to adults 65 years of age and older reported to the Vaccine Adverse Event Reporting System (VAERS), 2005–2010

Vaccine ◽

10.1016/j.vaccine.2011.05.100 ◽

2011 ◽

Vol 29 (50) ◽

pp. 9404-9408 ◽

Cited By ~ 15

Author(s):

Pedro L. Moro ◽

Xin Yue ◽

Paige Lewis ◽

Penina Haber ◽

Karen Broder

Keyword(s):

Adverse Event ◽

Adverse Events ◽

Tetanus Toxoid ◽

Reporting System ◽

Adverse Event Reporting System ◽

Adverse Event Reporting ◽

Diphtheria Toxoid ◽

Event Reporting ◽

Tdap Vaccine

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Enhanced surveillance of tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis (Tdap) vaccines in pregnancy in the Vaccine Adverse Event Reporting System (VAERS), 2011–2015

Vaccine ◽

10.1016/j.vaccine.2016.03.049 ◽

2016 ◽

Vol 34 (20) ◽

pp. 2349-2353 ◽

Cited By ~ 24

Author(s):

Pedro L. Moro ◽

Janet Cragan ◽

Naomi Tepper ◽

Yenlik Zheteyeva ◽

Oidda Museru ◽

...

Keyword(s):

Adverse Event ◽

Tetanus Toxoid ◽

Reporting System ◽

Adverse Event Reporting System ◽

Adverse Event Reporting ◽

Diphtheria Toxoid ◽

Event Reporting ◽

In Pregnancy

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Adverse events following adenovirus type 4 and type 7 vaccine, live, oral in the Vaccine Adverse Event Reporting System (VAERS), United States, October 2011–July 2018

Vaccine ◽

10.1016/j.vaccine.2019.08.087 ◽

2019 ◽

Vol 37 (44) ◽

pp. 6760-6767 ◽

Cited By ~ 2

Author(s):

Michael M. McNeil ◽

Iwona Paradowska-Stankiewicz ◽

Elaine R. Miller ◽

Paige L. Marquez ◽

Srihari Seshadri ◽

...

Keyword(s):

United States ◽

Adverse Event ◽

Adverse Events ◽

Reporting System ◽

Adverse Event Reporting System ◽

Adenovirus Type ◽

Adverse Event Reporting ◽

Event Reporting

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Safety review of the purified chick embryo cell rabies vaccine: Data from the Vaccine Adverse Event Reporting System (VAERS), 1997–2005

Vaccine ◽

10.1016/j.vaccine.2007.02.075 ◽

2007 ◽

Vol 25 (21) ◽

pp. 4244-4251 ◽

Cited By ~ 38

Author(s):

Azra Dobardzic ◽

Hector Izurieta ◽

Emily Jane Woo ◽

John Iskander ◽

Sean Shadomy ◽

...

Keyword(s):

Adverse Event ◽

Chick Embryo ◽

Reporting System ◽

Adverse Event Reporting System ◽

Adverse Event Reporting ◽

Embryo Cell ◽

Rabies Vaccine ◽

Event Reporting ◽

Safety Review ◽

Chick Embryo Cell

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Guillain–Barré Syndrome After Influenza Vaccination in the United States, A Report From the CDC/FDA Vaccine Adverse Event Reporting System (1990–2009)

Journal of Clinical Neuromuscular Disease ◽

10.1097/cnd.0b013e31824db14e ◽

2012 ◽

Vol 14 (2) ◽

pp. 66-71 ◽

Cited By ~ 6

Author(s):

Nizar Souayah ◽

Hussam A. Yacoub ◽

Hafiz M.R. Khan ◽

Khosro Farhad ◽

Lubna Shafiq Mehyar ◽

...

Keyword(s):

United States ◽

Adverse Event ◽

Influenza Vaccination ◽

Reporting System ◽

Adverse Event Reporting System ◽

The United States ◽

Adverse Event Reporting ◽

Guillain Barre Syndrome ◽

Event Reporting ◽

Guillain Barré

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Intussusception after monovalent rotavirus vaccine—United States, Vaccine Adverse Event Reporting System (VAERS), 2008–2014

Vaccine ◽

10.1016/j.vaccine.2015.07.054 ◽

2015 ◽

Vol 33 (38) ◽

pp. 4873-4877 ◽

Cited By ~ 25

Author(s):

Penina Haber ◽

Umesh D. Parashar ◽

Michael Haber ◽

Frank DeStefano

Keyword(s):

United States ◽

Adverse Event ◽

Reporting System ◽

Adverse Event Reporting System ◽

Adverse Event Reporting ◽

Rotavirus Vaccine ◽

Event Reporting

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Bullous disorders associated with PD-1 and PD-L1 inhibitors: Pharmacovigilance analysis of the United States Food and Drug Administration Adverse Event Reporting System from the Research on Adverse Drug Events And Reports Program

Journal of the American Academy of Dermatology ◽

10.1016/j.jaad.2020.01.059 ◽

2020 ◽

Vol 83 (3) ◽

pp. 955-957 ◽

Cited By ~ 1

Author(s):

Javier Jimenez ◽

Eran C. Gwillim ◽

Cory Kosche ◽

Anna Figueiredo ◽

Corrine Rauck ◽

...

Keyword(s):

United States ◽

Adverse Event ◽

Adverse Drug Events ◽

Reporting System ◽

Adverse Event Reporting System ◽

The United States ◽

Adverse Event Reporting ◽

Event Reporting ◽

United States Food ◽

States Food

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2463. Post-licensure Surveillance of 9-Valent Human Papillomavirus Vaccine (9vHPV) in the Vaccine Adverse Event Reporting System (VAERS), United States, 2014–2017

Open Forum Infectious Diseases ◽

10.1093/ofid/ofy210.2116 ◽

2018 ◽

Vol 5 (suppl_1) ◽

pp. S738-S738 ◽

Cited By ~ 1

Author(s):

Jorge Arana ◽

John Su ◽

Paige Lewis ◽

Maria Cano ◽

Lauri E Markowitz ◽

...

Keyword(s):

United States ◽

Adverse Event ◽

Human Papillomavirus ◽

Reporting System ◽

Adverse Event Reporting System ◽

Adverse Event Reporting ◽

Human Papillomavirus Vaccine ◽

Event Reporting ◽

Papillomavirus Vaccine

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Adverse events following purified chick embryo cell rabies vaccine in the Vaccine Adverse Event Reporting System (VAERS) in the United States, 2006–2016

Travel Medicine and Infectious Disease ◽

10.1016/j.tmaid.2018.10.016 ◽

2019 ◽

Vol 29 ◽

pp. 80-81

Author(s):

Pedro L. Moro ◽

Paige Lewis ◽

Maria Cano

Keyword(s):

United States ◽

Adverse Event ◽

Reporting System ◽

Adverse Event Reporting System ◽

The United States ◽

Adverse Event Reporting ◽

Embryo Cell ◽

Rabies Vaccine ◽

Event Reporting ◽

Chick Embryo Cell

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Stroke after Vaccination in United States. A Report from the CDC/FDA Vaccine Adverse Event Reporting System. [1990-2010] (P01.009)

Neurology ◽

10.1212/wnl.78.1_meetingabstracts.p01.009 ◽

2012 ◽

Vol 78 (Meeting Abstracts 1) ◽

pp. P01.009-P01.009

Author(s):

Z. Al Qudah ◽

W. Abukwaik ◽

N. Souayah

Keyword(s):

United States ◽

Adverse Event ◽

Reporting System ◽

Adverse Event Reporting System ◽

Adverse Event Reporting ◽

Event Reporting

Download Full-text

Safety review of tetanus toxoid, reduced diphtheria toxoid, acellular pertussis vaccines (Tdap) in adults aged ≥65 years, Vaccine Adverse Event reporting System (VAERS), United States, September 2010–December 2018

Adverse events after Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis (Tdap) Vaccine administered to adults 65 years of age and older reported to the Vaccine Adverse Event Reporting System (VAERS), 2005–2010

Enhanced surveillance of tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis (Tdap) vaccines in pregnancy in the Vaccine Adverse Event Reporting System (VAERS), 2011–2015

Adverse events following adenovirus type 4 and type 7 vaccine, live, oral in the Vaccine Adverse Event Reporting System (VAERS), United States, October 2011–July 2018

Safety review of the purified chick embryo cell rabies vaccine: Data from the Vaccine Adverse Event Reporting System (VAERS), 1997–2005

Guillain–Barré Syndrome After Influenza Vaccination in the United States, A Report From the CDC/FDA Vaccine Adverse Event Reporting System (1990–2009)

Intussusception after monovalent rotavirus vaccine—United States, Vaccine Adverse Event Reporting System (VAERS), 2008–2014

Bullous disorders associated with PD-1 and PD-L1 inhibitors: Pharmacovigilance analysis of the United States Food and Drug Administration Adverse Event Reporting System from the Research on Adverse Drug Events And Reports Program

2463. Post-licensure Surveillance of 9-Valent Human Papillomavirus Vaccine (9vHPV) in the Vaccine Adverse Event Reporting System (VAERS), United States, 2014–2017

Adverse events following purified chick embryo cell rabies vaccine in the Vaccine Adverse Event Reporting System (VAERS) in the United States, 2006–2016

Stroke after Vaccination in United States. A Report from the CDC/FDA Vaccine Adverse Event Reporting System. [1990-2010] (P01.009)

Safety review of tetanus toxoid, reduced diphtheria toxoid, acellular pertussis vaccines (Tdap) in adults aged ≥65 years, Vaccine Adverse Event reporting System (VAERS), United States, September 2010–December 2018