Affiliations 

  • 1 Public Health Foundation of Bangladesh Dhaka Bangladesh
  • 2 Ad-Din Women's Medical College Dhaka Bangladesh
  • 3 Bangladesh University of Textiles Dhaka Bangladesh
  • 4 Shaheed Suhrawardy Medical College Dhaka Bangladesh
  • 5 International Medical College Dhaka Bangladesh
  • 6 National Institute of Neurosciences & Hospital Dhaka Bangladesh
  • 7 The University of the West Indies Bridgetown Barbados
  • 8 National Defence University of Malaysia Kuala Lumpur Malaysia
  • 9 Chittagong Medical College Chittagong Bangladesh
  • 10 Gonoshasthaya Samaj Vittik Medical College Dhaka Bangladesh
  • 11 Sheikh Sayera Khatun Medical College Gopalganj Bangladesh
  • 12 American University of Integrative Sciences Bridgetown Barbados
  • 13 Bangladesh Medical College Dhaka Bangladesh
  • 14 Centre for Injury Prevention and Research Bangladesh (CIPRB) Dhaka Bangladesh
  • 15 Bangabandhu Sheikh Mujib Medical University Dhaka Bangladesh
  • 16 Shaheed Monsur Ali Medical College Hospital Dhaka Bangladesh
  • 17 Colonel Malek Medical College Manikganj Bangladesh
  • 18 Uttara Adhunik Medical College Dhaka Dhaka Bangladesh
  • 19 Jalalabad Ragib-Rabeya Medical College Sylhet Bangladesh
  • 20 United Hospital Ltd Dhaka Bangladesh
  • 21 Lake Erie College of Osteopathic Medicine Pennsylvania USA
FASEB Bioadv, 2022 Jun;4(6):379-390.
PMID: 35601057 DOI: 10.1096/fba.2021-00158

Abstract

Increased COVID-19 vaccine hesitancy presents a major hurdle in global efforts to contain the COVID-19 pandemic. This study was designed to estimate the prevalence of adverse events after the first dose of the Covishield (AstraZeneca) vaccine among physicians in Bangladesh. A cross-sectional study was conducted using an online questionnaire for physicians (n = 916) in Bangladesh. Physicians who received at least one dose of the COVID-19 vaccine were included. The study was carried out from April 12 to May 31, 2021. More than 58% of respondents (n = 533) reported one or more adverse events. Soreness of the injected arm (71.9%), tiredness (56.1%), fever (54.4%), soreness of muscles (48.4%), headache (41.5%) and sleeping more than usual (26.8%) were the most commonly reported adverse events. Most vaccine-related reactogenicities were reported by the younger cohorts (<45 years). The majority of respondents reported severity of reactogenicity as "mild," experienced on the day of vaccination, and lasting for 1-3 days. The most common reactogenicity was pain at the injection site; the second most common was tiredness. Almost half (49.2%) of the physicians took acetaminophen (paracetamol) to minimize the effects of vaccine reactogenicity. Multivariate logistic regression analyses showed that physicians with diabetes and hypertension (OR = 2.729 95% CI: 1.282-5.089) and asthma with other comorbidities (OR = 1.885 95% CI: 1.001-3.551) had a significantly higher risk of vaccine-related reactogenicities than physicians without comorbidities. Further safety studies with larger cohorts are required to monitor vaccine safety and provide assurance to potential vaccine recipients.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.