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Background: The increasing incidence of novel vaccine-preventable diseases, such as COVID-19, has led to an increase in the development of vaccines globally. Vaccine hesitancy has risen due to fears of vaccines causing harm. African health systems have generally relied on spontaneous reporting of adverse events following immunisation (AEFIs) to monitor vaccine safety.
Objectives: This study explored the views of healthcare professionals and managers regarding barriers and strategies to improve AEFI reporting in northern Ghana.
Methods: This study used a qualitative research design where in-depth interviews were conducted with health professionals and managers in five administrative regions in northern Ghana between March and August 2021. The purposive sampling method was used to select districts and participants. The interviews were audio recorded, transcribed, and coded into themes using QSR NVivo V.12 software before thematic content analysis.
Results: The study found that lack of feedback is the main regulatory-level factor affecting reporting adverse events. Health system-level factors, such as limited knowledge of reporting AEFIs, a lack of training, difficulties in using electronic application software to complete AEFI forms, and fear of punishment, significantly affect AEFI reporting. At the patient/community level, the main factors affecting AEFI reporting are the distance to health facilities and transportation costs. However, participants suggested continuous AEFI education, sensitisation of health workers and patients, timely feedback, and effective stakeholder collaboration among front-line health workers, health managers, and the national pharmacovigilance authority could improve AEFI reporting in Ghana.
Conclusions: Reporting of AEFIs contributes to improving vaccine safety, surveillance systems and prompt case management. However, the study identified multiple key factors at the regulatory, health system, and patient levels affecting AEFI reporting. Thus, improvements in line with these suggestions, including effective stakeholder engagement, are necessary to increase AEFI reporting.
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http://dx.doi.org/10.1136/bmjph-2024-001464 | DOI Listing |
Can Commun Dis Rep
August 2025
Public Health Agency of Canada.
Background: In Canada in 2020, the indication for use of Imvamune was expanded to include immunization against smallpox, mpox and related infection and disease in adults who are 18 years of age and older and determined to be at high risk for exposure.
Methods: Since the introduction of this new use for the vaccine and throughout the 2022 mpox outbreaks, the Public Health Agency of Canada (PHAC) has closely monitored the safety of the Imvamune vaccine through the Canadian Adverse Events Following Immunization Surveillance System (CAEFISS).
Results: This article describes reports of adverse events following immunization (AEFI) after administration of Imvamune, submitted to the CAEFISS database between May 24, 2022 and December 11, 2022, during the activation of Canada's emergency response.
Vaccines (Basel)
July 2025
Netherlands Pharmacovigilance Centre Lareb, Goudsbloemvallei 7, 5237 MH 's-Hertogenbosch, The Netherlands.
The aim of this study was to systematically assess Adverse Events Following Immunization (AEFI) among children following administration of the human papillomavirus (HPV) vaccine (Cervarix) included in the Dutch National Immunization Program (NIP) and to characterize the pattern and recurrence risk of AEFI after HPV revaccination. A longitudinal cohort event monitoring study, using patient-reported outcomes was used among recipients of the HPV vaccine at 10 years of age. Data were available for 3063 children following the first HPV vaccination and for 2209 children following the second HPV vaccination.
View Article and Find Full Text PDFHum Vaccin Immunother
December 2025
EPI Department, Chongqing Municipal Center for Disease Control and Prevention, Chongqing, China.
The Chinese National Adverse Events Following Immunization Information System (CNAEFIS) is the national-level passive vaccine safety surveillance system. This study aims to identify post-marketing vaccine adverse reaction signals in Chongqing through systematic analysis of 15-year AEFI data, verify the safety profile of locally recommended vaccines, and provide localized evidence for clinical practice and immunization policy formulation. The study included all 36 marketed vaccines in mainland China and collected all rare adverse reactions (RAR) reported in Chongqing through CNAEFIS from 2006 to 2021.
View Article and Find Full Text PDFPLoS One
August 2025
Acasus Nigeria, FCT, Abuja, Nigeria.
Background: Adverse events following immunization (AEFI) are any negative medical event that occurs after vaccination but may or may not be causally related to the vaccine. AEFI reporting is the gateway to AEFI surveillance systems at primary healthcare facilities where immunization services are provided. Several studies have highlighted low reporting of AEFI cases, particularly in low-resource settings, yet nothing is known about stakeholders' perspectives on the factors associated with the AEFI reporting rate in Nigeria.
View Article and Find Full Text PDFVaccine
August 2025
Ministry of Health and Family Welfare, Government of India, New Delhi, India.
Background: Under-reporting of severe and serious Adverse Events Following Immunization (AEFIs) from tertiary care teaching hospitals is a pressing issue in India. This pilot study aimed to evaluate the feasibility of a smartphone-based reporting intervention to enhance AEFI surveillance by treating doctors in four public teaching hospitals in Chennai, India.
Methods: From August 2023 to March 2024, a digital intervention was implemented across four medical college hospitals involving pediatrics, community medicine, and pharmacology departments.