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Cardiovascular Adverse Events Associated with Monoclonal Antibody Products in Patients with COVID-19
Little is known about cardiovascular safety profiles for monoclonal antibody products that received the FDA Emergency Use Authorization for COVID-19. In this study, data from the FDA Adverse Event Reporting System from the first quarter of 2020 to the second quarter of 2022 were used to investigate...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782649/ https://www.ncbi.nlm.nih.gov/pubmed/36558922 http://dx.doi.org/10.3390/ph15121472 |