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How frequent are acute reactions to COVID-19 vaccination and who is at risk?
Dreyer, Nancy; Reynolds, Matthew W; Albert, Lisa; Brinkley, Emma; Kwon, Tom; Mack, Christina; Toovey, Stephen.
  • Dreyer N; IQVIA Real-World Solutions, 201 Broadway, Cambridge, MA 02139, USA. Electronic address: Nancy.Dreyer@IQVIA.com.
  • Reynolds MW; IQVIA Real-World Solutions, 201 Broadway, Cambridge, MA 02139, USA. Electronic address: Matthew.Reynolds@IQVIA.com.
  • Albert L; IQVIA Real-World Solutions, 201 Broadway, Cambridge, MA 02139, USA. Electronic address: Lisa.Albert@IQVIA.com.
  • Brinkley E; IQVIA Real-World Solutions, 201 Broadway, Cambridge, MA 02139, USA. Electronic address: Emma.Brinkley@IQVIA.com.
  • Kwon T; IQVIA Real-World Solutions, 201 Broadway, Cambridge, MA 02139, USA. Electronic address: Tom.Kwon@IQVIA.com.
  • Mack C; IQVIA Real-World Solutions, 201 Broadway, Cambridge, MA 02139, USA. Electronic address: Christina.Mack@IQVIA.com.
  • Toovey S; Pegasus Research, Neuschwaendistrasse 6, 6390 Engelberg, Switzerland. Electronic address: Malaria@sunrise.ch.
Vaccine ; 40(12): 1904-1912, 2022 03 15.
Article in English | MEDLINE | ID: covidwho-1671275
Preprint
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ABSTRACT

INTRODUCTION:

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

METHODS:

Aweb-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).

RESULTS:

We 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% CI1.39; 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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / SARS-CoV-2 / COVID-19 Type of study: Prognostic study Topics: Long Covid / Vaccines Limits: Female / Humans / Male / Middle aged Language: English Journal: Vaccine Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / SARS-CoV-2 / COVID-19 Type of study: Prognostic study Topics: Long Covid / Vaccines Limits: Female / Humans / Male / Middle aged Language: English Journal: Vaccine Year: 2022 Document Type: Article