Serious adverse events following immunization with COVID-19 vaccines in Lebanon: a retrospective analysis of the National Pharmacovigilance Database.

Serious adverse events following immunization with COVID-19 vaccines in Lebanon: a retrospective analysis of the National Pharmacovigilance Database.

Publication date: Oct 21, 2024

Continuous surveillance and risk assessment of inactivated Coronavirus Disease 2019 (COVID-19)) vaccines provide an understanding of their safety profiles, guide vaccination strategy and public health policy. This study aims to analyze the characteristics and prevalence of officially reported serious adverse events following immunization (AEFIs) with inactivated COVID-19 vaccines by System Organ Class (SOC), age, and sex. To achieve this aim, a retrospective observational study was conducted between February 14th, 2021, and June 30th, 2022. Reported AEFIs were evaluated for data completeness. Causality assessment adhered to the World Health Organization guidelines. Findings revealed that the AEFIs occurrence did not significantly differ between vaccines used (ChAdOx1 vs. BNT162b2), sex, or SOC. The most prevalent AEFIs were vascular disorders (37%), followed by cardiac (25%) and nervous system disorders (14%). The adverse events were predominantly reported post-vaccination with the BNT162b2 vaccine, mainly after the first dose. The mean age was highest for miscellaneous disorders (70 +/- 21. 7 years) and the lowest for nervous system (46 +/- 22 years) and immune system disorders (45 +/- 19 years). Age differences were statistically different for vascular disorders (p = 0. 003) and immune system disorders (p = 0. 012). In conclusion, ongoing surveillance and risk assessment of the vaccine’s safety profile is crucial for detecting potential safety signals. Active surveillance of the reported serious AEFIs is highly needed to support evidence-based vaccination strategies and maintain public confidence in immunization programs.

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Concepts Keywords
Bnt162b2 Adolescent
Class Adult
Coronavirus Aged
Inactivated Aged, 80 and over
June BNT162 Vaccine
BNT162 Vaccine
ChAdOx1 nCoV-19
ChAdOx1 nCoV-19
COVID-19
COVID-19 Vaccines
COVID-19 Vaccines
COVID-19 vaccines
Databases, Factual
Female
Humans
Lebanon
Male
Middle Aged
Pharmacovigilance
Pharmacovigilance
Retrospective Studies
Young Adult

Semantics

Type Source Name
disease MESH Coronavirus Disease 2019
disease MESH Causality
disease MESH nervous system disorders
disease MESH immune system disorders
pathway REACTOME Reproduction
disease MESH Emergency
drug DRUGBANK Coenzyme M
drug DRUGBANK Trestolone
disease IDO symptom
disease MESH death
disease MESH birth defect
disease IDO process
disease IDO history
disease MESH allergy
disease IDO site
disease MESH cardiac disorders
disease MESH fatal outcome
disease MESH myocardial infarction
disease MESH functional neurological disorders
disease MESH anaphylaxis
disease MESH hemolytic anemia
disease MESH pneumonia
disease MESH febrile neutropenia
disease MESH thrombosis
disease MESH pulmonary embolism
disease MESH transient ischemic attack
disease MESH Kounis syndrome
disease MESH amyotrophic lateral sclerosis
pathway KEGG Amyotrophic lateral sclerosis
disease MESH aspiration pneumonia
disease MESH sepsis
disease MESH pericarditis
disease MESH deep vein thrombosis
disease MESH cerebrovascular accident
disease MESH acute disseminated encephalomyelitis
disease MESH optic neuritis
pathway REACTOME Immune System
disease MESH urticaria
disease MESH bronchitis
disease MESH actinomycosis
disease MESH infection
disease MESH bleeding
disease MESH unstable angina
disease MESH hypoxia
disease MESH pulmonary edema
disease MESH ST segment Elevation Myocardial Infarction
disease MESH NSTEMI
disease MESH Cardiac arrest
disease MESH Myocarditis
disease MESH Cerebral Hemorrhage
disease MESH Epileptic Seizure
disease MESH Guillain Barre Syndrome
disease MESH Thrombocytopenia
disease IDO blood
disease IDO intervention
disease MESH Adverse Drug Reaction

Original Article

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