Evidence map›Paper›PMID 39536790›Full record

ArticleJournal of Korean medical science2024

Active Surveillance for Safety Monitoring of XBB.1.5-Containing COVID-19 mRNA Vaccines in Korea.

Bomi Park, Hye Ah Lee, Yeonjae Kim, Chung Ho Kim, Hyunjin Park, Seunghee Jun, Hyelim Lee, Seunghyun Lewis Kwon, Yesul Heo, COVID-19 Vaccine Safety Research Committee and 2 more

Abstract read
In one paragraph

Article in Journal of Korean medical science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Bomi Park *COVID-19 Vaccine Safety Research Center, Seoul, Korea.ORCID https://orcid.org/0000-0001-5834-9975
Hye Ah Lee *Clinical Trial Center, Ewha Womans University Mokdong Hospital, Seoul, Korea.ORCID https://orcid.org/0000-0002-4051-0350
Yeonjae KimCOVID-19 Vaccine Safety Research Center, Seoul, Korea.ORCID https://orcid.org/0000-0002-8528-9477
Chung Ho KimCOVID-19 Vaccine Safety Research Center, Seoul, Korea.ORCID https://orcid.org/0009-0004-8508-7084
Hyunjin ParkCOVID-19 Vaccine Safety Research Center, Seoul, Korea.ORCID https://orcid.org/0000-0001-6536-8787
Seunghee JunCOVID-19 Vaccine Safety Research Center, Seoul, Korea.ORCID https://orcid.org/0000-0002-0530-8720
Hyelim LeeCOVID-19 Vaccine Safety Research Center, Seoul, Korea.ORCID https://orcid.org/0009-0002-4230-0952
Seunghyun Lewis KwonDivision of Immunization Services, Korea Disease Control and Prevention Agency, Cheongju, Korea.ORCID https://orcid.org/0000-0002-0113-0179
Yesul HeoDivision of Immunization Policy, Korea Disease Control and Prevention Agency, Cheongju, Korea.ORCID https://orcid.org/0000-0002-2164-2737
COVID-19 Vaccine Safety Research Committee
Hyungmin LeeDivision of Immunization Policy, Korea Disease Control and Prevention Agency, Cheongju, Korea. sea2sky@korea.kr.ORCID https://orcid.org/0000-0003-3478-3704
Hyesook ParkCOVID-19 Vaccine Safety Research Center, Seoul, Korea.ORCID https://orcid.org/0000-0002-9359-6522

Funding

Korea Disease Control and Prevention Agency 6400-6431-303
6 · The paper itself

Abstract

The emergence of the omicron variant and its sub-lineages has necessitated vaccine updates for coronavirus disease 2019. In September 2023, the U.S. Food and Drug Administration approved an updated BNT162b2 vaccine targeting the omicron XBB.1.5 variant, which was initiated in Korea in October 2024. This study demonstrates the adverse events reported through active nationwide surveillance after XBB.1.5 vaccination in Korea. Since October 19, 2023, the Korea Disease Control and Prevention Agency has conducted daily Short Message Service surveys to collect data on health issues, fever, vaccination site reactions, systemic symptoms, impact on daily life, and healthcare visits. Among 20,180 respondents, 27.9% reported health issues. Adverse reactions peaked on day 1 (28.7%), including pain at the vaccination site, muscle pain, fatigue, and fever. These findings elucidate the short-term safety of the XBB.1.5 vaccine and support its co-administration with the influenza vaccine, reducing vaccine hesitancy and achieving herd immunity.

Indexed as

BNT162 VaccineCOVID-19COVID-19 VaccinesAdolescentAdultAgedFemaleHumansMaleMiddle AgedRepublic of KoreaSARS-CoV-2Young AdultBNT162 VaccineCOVID-19 VaccinesCOVID-19Korea Disease Control and Prevention AgencyOmicronSafetyVaccinationXBB.1.5 Variant

Identifiers

PMID39536790
PMCPMC11557253

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.