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Page 1
Safety Surveillance of Varicella Vaccines in the Vaccine Adverse Event Reporting System, United States, 2006-2020.
Moro PL, Leung J, Marquez P, Kim Y, Wei S, Su JR, Marin M. Moro PL, et al. J Infect Dis. 2022 Oct 21;226(Suppl 4):S431-S440. doi: 10.1093/infdis/jiac306. J Infect Dis. 2022. PMID: 36265846 Review.
BACKGROUND: . The Vaccine Adverse Event Reporting System (VAERS) is the United States national passive vaccine safety surveillance system. ...
BACKGROUND: . The Vaccine Adverse Event Reporting System (VAERS) is the United States national passive va …
Safety monitoring in the Vaccine Adverse Event Reporting System (VAERS).
Shimabukuro TT, Nguyen M, Martin D, DeStefano F. Shimabukuro TT, et al. Vaccine. 2015 Aug 26;33(36):4398-405. doi: 10.1016/j.vaccine.2015.07.035. Epub 2015 Jul 22. Vaccine. 2015. PMID: 26209838 Free PMC article. Review.
Food and Drug Administration (FDA) conduct post-licensure vaccine safety monitoring using the Vaccine Adverse Event Reporting System (VAERS), a spontaneous (or passive) reporting system. ...
Food and Drug Administration (FDA) conduct post-licensure vaccine safety monitoring using the Vaccine Adverse Event …
Summary of COVID-19 Vaccine-Related Reports in the Vaccine Adverse Event Reporting System.
Ceacareanu AC, Wintrob ZAP. Ceacareanu AC, et al. J Res Pharm Pract. 2021 Dec 25;10(3):107-113. doi: 10.4103/jrpp.jrpp_49_21. eCollection 2021 Jul-Sep. J Res Pharm Pract. 2021. PMID: 35198503 Free PMC article. Review.
Since the beginning of the vaccination efforts in December 2020, almost 220,000 adverse events (AEs) have been reported through the Vaccine Adverse Event Reporting System, a reporting platform administered jointly by the FDA and the Centers for …
Since the beginning of the vaccination efforts in December 2020, almost 220,000 adverse events (AEs) have been reported through the Vacci …
Vaccine adverse event reporting system (VAERS): Evaluation of 31 years of reports and pandemics' impact.
Almadani OA, Alshammari TM. Almadani OA, et al. Saudi Pharm J. 2022 Dec;30(12):1725-1735. doi: 10.1016/j.jsps.2022.10.001. Epub 2022 Oct 7. Saudi Pharm J. 2022. PMID: 36601511 Free PMC article.
BACKGROUND: Vaccine adverse event reporting system (VAERS) was established in the United States (U.S.) as an early warning system with a main purpose of collecting post-marketing Adverse events following immunizations (AEFIs) reports to monitor …
BACKGROUND: Vaccine adverse event reporting system (VAERS) was established in the United States (U.S.) as …
Vaccine Adverse Events: Separating Myth from Reality.
Spencer JP, Trondsen Pawlowski RH, Thomas S. Spencer JP, et al. Am Fam Physician. 2017 Jun 15;95(12):786-794. Am Fam Physician. 2017. PMID: 28671426 Free article. Review.
If a recommended vaccine is refused, proper documentation is essential. The Vaccine Adverse Event Reporting System and National Vaccine Injury Compensation Program track adverse events and allow compensation for documented harms from vaccination …
If a recommended vaccine is refused, proper documentation is essential. The Vaccine Adverse Event Reporting S …
Post-authorization safety surveillance of Ad.26.COV2.S vaccine: Reports to the Vaccine Adverse Event Reporting System and v-safe, February 2021-February 2022.
Woo EJ, Gee J, Marquez P, Baggs J, Abara WE, McNeil MM, Dimova RB, Su JR. Woo EJ, et al. Vaccine. 2023 Jul 5;41(30):4422-4430. doi: 10.1016/j.vaccine.2023.06.023. Epub 2023 Jun 14. Vaccine. 2023. PMID: 37321898 Free PMC article. Review.
BACKGROUND: On 2/27/2021, FDA authorized Janssen COVID-19 Vaccine (Ad.26.COV2.S) for use in individuals 18 years of age and older. Vaccine safety was monitored using the Vaccine Adverse Event Reporting System (VAERS), a national passive surveill …
BACKGROUND: On 2/27/2021, FDA authorized Janssen COVID-19 Vaccine (Ad.26.COV2.S) for use in individuals 18 years of age and older. Vaccine s …
Spontaneous reports of primary ovarian insufficiency after vaccination: A review of the vaccine adverse event reporting system (VAERS).
Patricia Wodi A, Marquez P, Mba-Jonas A, Barash F, Nguon K, Moro PL. Patricia Wodi A, et al. Vaccine. 2023 Feb 24;41(9):1616-1622. doi: 10.1016/j.vaccine.2022.12.038. Epub 2023 Jan 31. Vaccine. 2023. PMID: 36732165 Review.
A Vaccine Safety Datalink study did not find an increased risk for POI after vaccination. We reviewed the Vaccine Adverse Event Reporting System (VAERS) to describe POI reports. ...
A Vaccine Safety Datalink study did not find an increased risk for POI after vaccination. We reviewed the Vaccine Adverse E …
Ocular Complications after COVID-19 Vaccination, Vaccine Adverse Event Reporting System.
Nyankerh CNA, Boateng AK, Appah M. Nyankerh CNA, et al. Vaccines (Basel). 2022 Jun 13;10(6):941. doi: 10.3390/vaccines10060941. Vaccines (Basel). 2022. PMID: 35746549 Free PMC article.
We investigated the ocular adverse event reports in patients reported to the Vaccine Adverse Event Reporting System (VAERS) following vaccination against COVID-19. ...
We investigated the ocular adverse event reports in patients reported to the Vaccine Adverse Event Reporting …
Understanding vaccine safety information from the Vaccine Adverse Event Reporting System.
Varricchio F, Iskander J, Destefano F, Ball R, Pless R, Braun MM, Chen RT. Varricchio F, et al. Pediatr Infect Dis J. 2004 Apr;23(4):287-94. doi: 10.1097/00006454-200404000-00002. Pediatr Infect Dis J. 2004. PMID: 15071280 Review.
The Vaccine Adverse Event Reporting System (VAERS) is administered by the Food and Drug Administration and CDC and is a key component of postlicensure vaccine safety surveillance. ...
The Vaccine Adverse Event Reporting System (VAERS) is administered by the Food and Drug Administration an …
531 results