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Adverse drug reactions and drug interactions in the treatment of hospitalized patients with coronavirus disease 2019 (COVID-19)

OBJECTIVES: To identify drugs that were administered off label to hospitalized patients with suspected coronavirus disease 2019 (COVID-19) and to identify adverse drug reactions (ADRs) and drug–drug interactions associated with these therapies. METHODS: This case–control study was conducted in a Bra...

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Detalles Bibliográficos
Autores principales: Marins, Tatiana A., Marra, Alexandre R., Edmond, Michael B., Colombo, Ligia Regina Prystaj, Vieira, Sthephanie Favalli, de Oliveira Xavier, Fernanda, Chauvin, Alessandra Gomes, Pinho, João Renato Rebello, de Almeida, Silvana M., Junior, Marcelino Souza Durão
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9495530/
https://www.ncbi.nlm.nih.gov/pubmed/36168493
http://dx.doi.org/10.1017/ash.2021.196
Descripción
Sumario:OBJECTIVES: To identify drugs that were administered off label to hospitalized patients with suspected coronavirus disease 2019 (COVID-19) and to identify adverse drug reactions (ADRs) and drug–drug interactions associated with these therapies. METHODS: This case–control study was conducted in a Brazilian hospital from March to April 2020 among patients with suspected COVID-19, comparing those with positive severe acute respiratory coronavirus virus 2 (SARS-CoV-2) reverse-transcriptase polymerase chain reaction (RT-PCR) results and those with negative results. RESULTS: The most commonly used medications in both groups were azithromycin and hydroxychloroquine. There was a significantly higher prevalence of reactions among patients with positive RT-PCR for SARS-CoV-2 (48.5% vs 28.8%; P = .008) in the propensity score–matched cohort, and the most commonly reported ADRs among these patients were diarrhea (43.8%), elevated liver enzymes (31.3%), and nausea and vomiting (29.7%). CONCLUSIONS: Our data demonstrate that ADRs and drug–drug interactions are common with off-label treatments for COVID-19.