Evidence map›Paper›PMID 35177299›Full record

ArticleVaccine2022

How frequent are acute reactions to COVID-19 vaccination and who is at risk?

Nancy Dreyer, Matthew W Reynolds, Lisa Albert, Emma Brinkley, Tom Kwon, Christina Mack, Stephen Toovey

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Vaccine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04368065 (Registry to Study Factors That May Impact COVID-19 Occurrence and Severity), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 16% of its field
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.

NCT04368065 completednot on this map

Registry to Study Factors That May Impact COVID-19 Occurrence and Severity

Typeobservational_patient_registrySponsorIQVIA Pty LtdRan2020 to 2023Enrolled35,278ConditionsCOVID-19
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Observational
  7. Review
  8. 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

7 authors at 2 institutions in 1 country.

Nancy DreyerIQVIA Real-World Solutions, 201 Broadway, Cambridge, MA 02139, USA. Electronic address: Nancy.Dreyer@IQVIA.com.
Matthew W ReynoldsIQVIA Real-World Solutions, 201 Broadway, Cambridge, MA 02139, USA. Electronic address: Matthew.Reynolds@IQVIA.com.
Lisa AlbertIQVIA Real-World Solutions, 201 Broadway, Cambridge, MA 02139, USA. Electronic address: Lisa.Albert@IQVIA.com.
Emma BrinkleyIQVIA Real-World Solutions, 201 Broadway, Cambridge, MA 02139, USA. Electronic address: Emma.Brinkley@IQVIA.com.
Tom KwonIQVIA Real-World Solutions, 201 Broadway, Cambridge, MA 02139, USA. Electronic address: Tom.Kwon@IQVIA.com.
Christina MackIQVIA Real-World Solutions, 201 Broadway, Cambridge, MA 02139, USA. Electronic address: Christina.Mack@IQVIA.com.
Stephen TooveyPegasus Research, Neuschwaendistrasse 6, 6390 Engelberg, Switzerland. Electronic address: Malaria@sunrise.ch.
IQ Solutions · USIQVIA (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOur objective was to describe and compare self-reported side effects ofCOVID-19 vaccinesin theUSA.

methodsAweb-basedregistry enrolled volunteers who received a COVID-19 vaccine between March 19-July 15, 2021. We collected self-reported short-term side effects, medical consultation, hospitalization, and quality of life impact following completed vaccination regimens (Pfizer, Moderna, J&J).

resultsWe recruited 6,966 volunteers who completed their full course of vaccination (median age 48 years, IQR 35.0-62.0; 83.6% female): Pfizer 3,486; Moderna 2,857; J&J 623. Few (3.1%) sought medical care for post-vaccination side effects. Hospitalization (n = 17; 0.3%) and severe allergic reactions (n = 39; 0.6%) also were rare. Those with autoimmune disease or lung disease were approximately twice as likely to seek medical care (adjusted odds ratio (aOR) 2.01, 95% CI:1.39; 2.92 and aOR 1.70, 95% CI: 1.12; .58 respectively). 92.4% of participantsreported ≥ 1side effect (median 3), with injection site reactions (78.9%), fatigue (70.3%), headache (49.0%) reported most frequently. More side effects were reported after the second dose of two-dose vaccines (medians: 1 vs. 2 for Pfizer and 1 vs. 3 for Moderna for first and second doses respectively) versus 3 for J&J's single-dose vaccine. For the employed, the median number of workdays missed was one. Diabetics and those vaccinated against influenza were substantially less likely to report 3 or more symptoms (aOR 0.68, 95% CI: 0.56;0.82] and aOR 0.82, 95% CI: 0.73;0.93, respectively). DISCUSSION: The total side effect burden was, not unexpectedly, greater with two-dose regimens but all three vaccines appear relatively safe. Very few subjects reported side effects serious enough to warrant medical care or reported post-vaccination hospitalization. While these findings do not address possible long-term effects, they do inform on their short-term safety and tolerability and will hopefully provide some reassurance and positively inform the benefit-risk and pharmacoeconomic assessment for all three vaccines. See Clinicaltrials.gov NCT04368065.

Indexed as

COVID-19COVID-19 VaccinesSARS-CoV-2FemaleHumansMaleMiddle AgedQuality of LifeVaccinationCOVID-19 VaccinesCOVID-19COVID-19 vaccinesEpidemiologyPatient-reported outcomesVaccine effectivenessVaccine side effects

Identifiers

PMID35177299
PMCPMC8825448
OpenAlexW4220864869

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.