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doi: 10.1016/0196-9781(87)90163-x

The Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) is a spontaneous reporting database monitoring the safety of drugs and biologics after their market approval 14

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3.6.1 Background Stroke is a leading cause of adult-onset neuropsychiatric and neurodegenerative disability, with substantial global prevalence and profound long-term consequences (Elendu et al., 2023)

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The mouse and human LTC 4 synthases have been characterized (Sderstrm et al., 1988)