Hydroxychloroquine reports to EudraVigilance database during COVID-19

• Autor(a) principal: Matos, Cristiano
• Data de Publicação: 2022
• Outros Autores: Marmé, Maria Inês
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
• Texto Completo: https://doi.org/10.34624/jshd.v4i1.28903

Introduction: Hydroxychloroquine is an antimalarial drug that belongs to the 4-aminoquinolone group. [1] Despite of this properties presents several immunomodulatory and anti-inflammatory characteristics. [1,2] In 2020, with the emergence of the COVID-19 pandemic, researchers used existing drugs with potential for the treatment of COVID-19, including hydroxychloroquine, which ended up being used off-label. [3,4] From the clinical trials hydroxychloroquine has many adverse effects that can increase risk for the SARS-COV-2 patients health. Common adverse effects are related to gastrointestinal and cardiovascular systems, neurotoxicity and retinopathy. [2,5]. The objective of this research was to describe the adverse effects profile of hydroxychloroquine in COVID-19 patients and to characterize the risks associated with off-label use of hydroxychloroquine. Methods: An observational, retrospective and descriptive study was conducted. Information collected from the “Eudravigilance” database was analyzed using descriptive statistics with R Studio® software. Information about the source of reporting, patient sex, serious adverse reactions, deaths and off-label cases and their outcome, were evaluated and compared in the pre- and post-pandemic period. Results: The number of reports of adverse reactions to hydroxychloroquine increased significantly during the pandemic period (increase of 310.3%), with health professionals reporting the most (92.0%). The potential for harm has increased as off-label administration of hydroxychloroquine is associated with an increased incidence and severity of adverse reactions. Serious outcomes, as deaths presented an increased number during pandemic. The total number of suspected adverse drug reactions reports increased from a mean of 7.7 reactions per month pre pandemic to 114.5 reactions after the pandemic. Serious outcomes also increased during pandemic: a total of 361 (6.8%) reactions were considered serious before pandemic, and 2740 (26.6%) after pandemic begins. Finally, deaths associated with the use of hydroxychloroquine were also evaluated, of which 67.0% are described in off-label use. Discussion: The profile of safety of hydroxychloroquine appears to change during the pandemic with the off-label use. Hydroxychloroquine present different adverse reactions, which should be reported whenever possible. Its off-label use for COVID-19 has been shown to be a risk for patients, as it causes them more risks than usual use. In short, hydroxychloroquine appears to not bring benefits to COVID-19 and it ends up bringing several complications when it is administered.