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[Related PubMed/MEDLINE] Total Number of Papers: 401
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No. |
Year |
Title |
Co-occurring Abbreviation |
1 |
2023 |
Analysis of hematologic adverse events reported to a national surveillance system following COVID-19 bivalent booster vaccination. |
AIHA, ITP, SARS-CoV-2, VITT |
2 |
2023 |
Automatic Identification of Self-Reported COVID-19 Vaccine Information from Vaccine Adverse Events Reporting System. |
COVID-19, GS, NLP |
3 |
2023 |
COVID-19 Vaccine Safety First Year Findings in Adolescents. |
--- |
4 |
2023 |
Death and Disability Reported with Cases of Vaccine Anaphylaxis Stratified by Administration Setting: An Analysis of the Vaccine Adverse Event Reporting System from 2017 to 2022. |
CI |
5 |
2023 |
Herpetic Eye Disease After SARS-CoV-2 Vaccination: A CDC-VAERS Database Analysis. |
CDC, HSO, HZO |
6 |
2023 |
Mining adverse events in large frequency tables with ontology, with an application to the vaccine adverse event reporting system. |
AE |
7 |
2023 |
Post-vaccination headache reporting: Trends according to the Vaccine Adverse Events Reporting System. |
--- |
8 |
2023 |
Real-life safety profile of mRNA vaccines for COVID-19: An analysis of VAERS database. |
CI |
9 |
2023 |
Reported rates of all-cause serious adverse events following immunization with BNT-162b in 5-17-year-old children in the United States. |
RSV, sAEFI, US |
10 |
2023 |
Reporting rates for VAERS death reports following COVID-19 vaccination, December 14, 2020-November 17, 2021. |
--- |
11 |
2023 |
Reports of Guillain-Barré Syndrome After COVID-19 Vaccination in the United States. |
GBS, OE, RRRs |
12 |
2023 |
Reports of Guillain-Barre Syndrome Following COVID-19 Vaccination in the USA: An Analysis of the VAERS Database. |
GBS/V, IQR |
13 |
2023 |
Safety Monitoring of Bivalent COVID-19 mRNA Vaccine Booster Doses Among Children Aged 5-11 Years - United States, October 12-January 1, 2023. |
ACIP, EUAs, FDA |
14 |
2023 |
Safety of co-administration of mRNA COVID-19 and seasonal inactivated influenza vaccines in the vaccine adverse event reporting system (VAERS) during July 1, 2021-June 30, 2022. |
AEs, AESI, PTs |
15 |
2023 |
Safety of COVID-19 vaccines in pregnancy: a VAERS based analysis. |
AEFIs |
16 |
2023 |
Spontaneous reports of primary ovarian insufficiency after vaccination: A review of the vaccine adverse event reporting system (VAERS). |
ACOG, HPV, POI |
17 |
2023 |
Vaccine adverse event reporting system (VAERS): Evaluation of 31 years of reports and pandemics' impact. |
AEFIs, COVID-19, US |
18 |
2022 |
A Case Report of Sudden Sensorineural Hearing Loss (SSNHL) After Administration of the COVID-19 Vaccine. |
COVID-19, EUA, SSNHL, US |
19 |
2022 |
A Comparative Analysis of COVID-19 Vaccines Based on over 580,000 Cases from the Vaccination Adverse Event Reporting System. |
ORs |
20 |
2022 |
A Possible Case of COVID-19 Booster Vaccine-Associated Rhabdomyolysis and Acute Kidney Injury. |
ADRs, COVID-19, GBS, mRNA, SARS-CoV-2, TTS |
21 |
2022 |
Acute kidney injury after COVID-19 vaccines: a real-world study. |
AKI, COVID-19 |
22 |
2022 |
Adverse Events and Safety Profile of the COVID-19 Vaccines in Adolescents: Safety Monitoring for Adverse Events Using Real-World Data. |
AEs |
23 |
2022 |
Analyses of reported severe adverse events after immunization with SARS-CoV-2 vaccines in the United States: One year on. |
ED, IRRs, sAEFI, US |
24 |
2022 |
Analyzing the U.S. Post-marketing safety surveillance of COVID-19 vaccines. |
AEs, PMS, US |
25 |
2022 |
Assessment of Sudden Sensorineural Hearing Loss After COVID-19 Vaccination. |
SSNHL |
26 |
2022 |
Association between seasonal influenza vaccines and the increased risk of acute disseminated encephalomyelitis, estimated using the Vaccine Adverse Event Reporting System. |
ADEM, Cell-based vaccine, CNS, Egg-based vaccine, ROR, WSPs |
27 |
2022 |
Autoimmune haemolytic anaemia and immune thrombocytopenia following SARS-CoV-2 and non-SARS-CoV-2 vaccination: 32 Years of passive surveillance data. |
AIHA, CDC, ITP, MMR |
28 |
2022 |
BNT162b2 Vaccine-Associated Myo/Pericarditis in Adolescents: A Stratified Risk-Benefit Analysis. |
--- |
29 |
2022 |
Booster dose of COVID-19 mRNA vaccine does not increase risks of myocarditis and pericarditis compared with primary vaccination: New insights from the vaccine adverse event reporting system. |
CDC |
30 |
2022 |
Characteristics and Comparison of Adverse Events of Coronavirus Disease 2019 Vaccines Reported to the United States Vaccine Adverse Event Reporting System Between 14 December 2020 and 8 October 2021. |
AEs, COVID-19, ER, RORs |
31 |
2022 |
Coagulation factor inhibitors in COVID-19: From SARS-CoV-2 vaccination to infection. |
SARS-CoV-2 |
32 |
2022 |
Comparability of clinical trials and spontaneous reporting data regarding COVID-19 vaccine safety. |
AEs, RCTs |
33 |
2022 |
Comparison of the post-marketing safety profile between influenza and COVID-19 vaccines: An analysis of the vaccine adverse event reporting system. |
AEs |
34 |
2022 |
COVID-19 Vaccination a Cause of Guillain-Barre Syndrome? A Case Series. |
GBS |
35 |
2022 |
COVID-19 vaccine and menstrual conditions in female: data analysis of the Vaccine Adverse Event Reporting System (VAERS). |
COVID-19, ROR |
36 |
2022 |
COVID-19 Vaccine as a Potential Triggering Factor for Anti-Glomerular Basement Membrane (GBM) Disease: A Case Report and Literature Review. |
Anti-GBM, GBM, RPGN |
37 |
2022 |
Curbing COVID-19 Vaccine Hesitancy from a Dermatological Standpoint: Analysis of Cutaneous Reactions in the Vaccine Adverse Event Reporting System (VAERS) Database. |
--- |
38 |
2022 |
Disentangling a Thorny Issue: Myocarditis and Pericarditis Post COVID-19 and Following mRNA COVID-19 Vaccines. |
--- |
39 |
2022 |
Frequency and Associations of Adverse Reactions of COVID-19 Vaccines Reported to Pharmacovigilance Systems in the European Union and the United States. |
CTC |
40 |
2022 |
Glaucoma Cases Following SARS-CoV-2 Vaccination: A VAERS Database Analysis. |
SARS-CoV-2 |
41 |
2022 |
Hearing disorder following COVID-19 vaccination: A pharmacovigilance analysis using the Vaccine Adverse Event Reporting System. |
CI, COVID-19, PRR, ROR |
42 |
2022 |
Herpes zoster and simplex reactivation following COVID-19 vaccination: new insights from a vaccine adverse event reporting system (VAERS) database analysis. |
--- |
43 |
2022 |
Modeling COVID-19 Vaccine Adverse Effects with a Visualized Knowledge Graph Database. |
--- |
44 |
2022 |
Myocarditis Cases Reported After mRNA-Based COVID-19 Vaccination in the US From December 2020 to August 2021. |
--- |
45 |
2022 |
Neurological Events Reported after COVID-19 Vaccines: An Analysis of VAERS. |
CVT, GBS |
46 |
2022 |
OAE-based data mining and modeling analysis of adverse events associated with three licensed HPV vaccines. |
AEs, GPS, HPV, OAE, SAEs |
47 |
2022 |
Ocular Complications after COVID-19 Vaccination, Vaccine Adverse Event Reporting System. |
--- |
48 |
2022 |
Oral Adverse Events Following COVID-19 Vaccination: Analysis of VAERS Reports. |
AEs |
49 |
2022 |
Pediatric COVID-19 Vaccination: A Description of Adverse Events or Reactions Reported in Kansans Aged 6 to 17. |
AERs |
50 |
2022 |
Post-authorization surveillance of adverse events following COVID-19 vaccines in pregnant persons in the vaccine adverse event reporting system (VAERS), December 2020 - October 2021. |
AEs |
51 |
2022 |
Posterior Reversible Encephalopathy Syndrome Onset Within 24 Hours Following Moderna mRNA Booster COVID-19 Vaccination: Vaccine Adverse Event Vs. Hypertension? |
COVID-19, PRES, SARS-CoV-2 |
52 |
2022 |
Postmarketing safety surveillance of high-dose quadrivalent influenza vaccine: Reports to the Vaccine Adverse Event Reporting System. |
--- |
53 |
2022 |
Profiling COVID-19 Vaccine Adverse Events by Statistical and Ontological Analysis of VAERS Case Reports. |
AEs, OAE, TTS |
54 |
2022 |
Prolonged Diarrhea Following COVID-19 Vaccination: A Case Report and Literature Review. |
COVID-19, CT, SARS-CoV-2 |
55 |
2022 |
Psychotropic drugs interaction with the lipid nanoparticle of COVID-19 mRNA therapeutics. |
mRNA, SPI |
56 |
2022 |
Reply to: correspondence on "Herpes Zoster and Simplex reactivation following COVID-19 vaccination: new insights from a vaccine adverse event reporting system (VAERS) database analysis". |
--- |
57 |
2022 |
Reports of myocarditis and pericarditis following mRNA COVID-19 vaccination: a systematic review of spontaneously reported data from the UK, Europe and the USA and of the scientific literature. |
EU/EEA, mRNA |
58 |
2022 |
Risk Factors and Incidence Rates of Self-Reported Short-Term Adverse Events of COVID-19 Vaccine Booster Dose. |
AE, IR, NSAE, SAE |
59 |
2022 |
Risk of Myocarditis and Pericarditis among Young Adults following mRNA COVID-19 Vaccinations. |
--- |
60 |
2022 |
Safety Monitoring of Bivalent COVID-19 mRNA Vaccine Booster Doses Among Persons Aged ≥12 Years - United States, August 31-October 23, 2022. |
ACIP, FDA |
61 |
2022 |
Safety Monitoring of COVID-19 mRNA Vaccine First Booster Doses Among Persons Aged ≥12 Years with Presumed Immunocompromise Status - United States, January 12, 2022-March 28, 2022. |
ACIP, FDA |
62 |
2022 |
Safety Monitoring of COVID-19 mRNA Vaccine Second Booster Doses Among Adults Aged ≥50 Years - United States, March 29, 2022-July 10, 2022. |
ACIP, FDA |
63 |
2022 |
Safety Monitoring of COVID-19 Vaccine Booster Doses Among Adults - United States, September 22, 2021-February 6, 2022. |
ACIP, FDA |
64 |
2022 |
Safety Monitoring of COVID-19 Vaccine Booster Doses Among Persons Aged 12-17 Years - United States, December 9, 2021-February 20, 2022. |
EUA, FDA |
65 |
2022 |
Safety Monitoring of JYNNEOS Vaccine During the 2022 Mpox Outbreak - United States, May 22-October 21, 2022. |
eIND, EUA, FDA, mpox, VSD |
66 |
2022 |
Safety Monitoring of Pfizer-BioNTech COVID-19 Vaccine Booster Doses Among Children Aged 5-11 Years - United States, May 17-July 31, 2022. |
EUA, FDA |
67 |
2022 |
Safety of Booster Doses of Coronavirus Disease 2019 (COVID-19) Vaccine in Pregnancy in the Vaccine Adverse Event Reporting System. |
COVID-19 |
68 |
2022 |
Safety of COVID-19 Vaccination in United States Children Ages 5 to 11 Years. |
--- |
69 |
2022 |
Safety of mRNA vaccines administered during the initial 6 months of the US COVID-19 vaccination programme: an observational study of reports to the Vaccine Adverse Event Reporting System and v-safe. |
--- |
70 |
2022 |
Safety Surveillance of Varicella Vaccines in the Vaccine Adverse Event Reporting System, United States, 2006-2020. |
AEs, MMRV, VAR |
71 |
2022 |
SARS-CoV-2 vaccine-associated-tinnitus: A review. |
--- |
72 |
2022 |
Serious adverse reaction associated with the COVID-19 vaccines of BNT162b2, Ad26.COV2.S, and mRNA-1273: Gaining insight through the VAERS. |
AEFI, ROR, TTO |
73 |
2022 |
Shoulder injury related to vaccine administration (SIRVA) after COVID-19 vaccination. |
SIRVA |
74 |
2022 |
Spread of COVID-19 Vaccine Misinformation in the Ninth Inning: Retrospective Observational Infodemic Study. |
--- |
75 |
2022 |
Symptomatic Myocarditis Post COVID-19 Vaccination. |
COVID-19, mRNA |
76 |
2022 |
Systematic review of spontaneous reports of myocarditis and pericarditis in transplant recipients and immunocompromised patients following COVID-19 mRNA vaccination. |
EU/EEA, PRR |
77 |
2022 |
The COVID-19 Vaccines: A Description of Adverse Events of Reactions Reported in Kansas. |
AERs, COVID-19, SARS-CoV-2 |
78 |
2022 |
The Safety of mRNA-1273, BNT162b2 and JNJ-78436735 COVID-19 Vaccines: Safety Monitoring for Adverse Events Using Real-World Data. |
AEs |
79 |
2022 |
Thromboembolic events after Ad.26.COV2.S COVID-19 vaccine: Reports to the Vaccine Adverse Event Reporting System. |
FDA, TEEs |
80 |
2022 |
Transient Myopericarditis Following Vaccination for COVID-19. |
CDC, mRNA, SARS-CoV-2 |
81 |
2022 |
Trends in reporting embolic and thrombotic events after COVID-19 vaccination: A retrospective, pharmacovigilance study. |
COVID-19, ETEs, ROR |
82 |
2022 |
Uncommon Side Effects of COVID-19 Vaccination in the Pediatric Population. |
CDC, COVID-19, MIS-C |
83 |
2022 |
Use of the Janssen (Johnson & Johnson) COVID-19 Vaccine: Updated Interim Recommendations from the Advisory Committee on Immunization Practices - United States, December 2021. |
ACIP, CVST, EUA, FDA, GBS, TTS |
84 |
2022 |
Usefulness of Vaccine Adverse Event Reporting System for Machine-Learning Based Vaccine Research: A Case Study for COVID-19 Vaccines. |
--- |
85 |
2021 |
A Rare Variant of Guillain-Barre Syndrome Following Ad26.COV2.S Vaccination. |
COVID-19, FDA, GBS, SARS-CoV-2 |
86 |
2021 |
Acute Myocardial Injury Following COVID-19 Vaccination: A Case Report and Review of Current Evidence from Vaccine Adverse Events Reporting System Database. |
--- |
87 |
2021 |
Age and Gender Disparities in Adverse Events Following COVID-19 Vaccination: Real-World Evidence Based on Big Data for Risk Management. |
AEs, COVID-19, ER |
88 |
2021 |
Allergic Reactions Including Anaphylaxis After Receipt of the First Dose of Moderna COVID-19 Vaccine - United States, December 21, 2020-January 10, 2021. |
ACIP, COVID-19, EUA, FDA |
89 |
2021 |
Allergic Reactions Including Anaphylaxis After Receipt of the First Dose of Pfizer-BioNTech COVID-19 Vaccine - United States, December 14-23, 2020. |
ACIP, COVID-19, EUA, FDA |
90 |
2021 |
Anxiety-Related Adverse Event Clusters After Janssen COVID-19 Vaccination - Five U.S. Mass Vaccination Sites, April 2021. |
EUA, FDA |
91 |
2021 |
Association of Receipt of the Ad26.COV2.S COVID-19 Vaccine With Presumptive Guillain-Barre Syndrome, February-July 2021. |
FDA, GBS |
92 |
2021 |
COVID-19 mRNA Vaccines Are Generally Safe in the Short Term: A Vaccine Vigilance Real-World Study Says. |
AEFIs |
93 |
2021 |
COVID-19 Vaccine Safety in Adolescents Aged 12-17 Years - United States, December 14, 2020-July 16, 2021. |
ACIP, EUA, FDA |
94 |
2021 |
COVID-19 Vaccine Safety in Children Aged 5-11 Years - United States, November 3-December 19, 2021. |
ACIP, EUA, FDA |
95 |
2021 |
Editorial: What Can be Learned from National and International Vaccine Adverse Event Reporting Systems During the COVID-19 Pandemic? |
CDC, FDA |
96 |
2021 |
Evaluaton of adverse events following immunization reported during national immunization programs (Between 2017-2019 in Ankara Province). |
AEFI, EPI |
97 |
2021 |
Extracting postmarketing adverse events from safety reports in the vaccine adverse event reporting system (VAERS) using deep learning. |
AEs, BERT, GBS |
98 |
2021 |
Facial nerve palsy following the administration of COVID-19 mRNA vaccines: analysis of a self-reporting database. |
AEFI, CI, COVID-19, ROR |
99 |
2021 |
Facial paralysis and vaccinations: a vaccine adverse event reporting system review. |
--- |
100 |
2021 |
First Month of COVID-19 Vaccine Safety Monitoring - United States, December 14, 2020-January 13, 2021. |
COVID-19, EUA, FDA, LTCF |
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