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Omission of adverse event reporting on finerenone
  • Mayer Brezis
Mayer Brezis

Corresponding Author:brezis@mail.huji.ac.il

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Abstract

We wish to describe the omission of adverse event reporting on finerenone in a recently published trial. We suspect that this case illustrates the tip of an iceberg of underreporting of adverse events in clinical trials. We propose as a requirement in clinical trials, to have routine direct reporting by patients for safety monitoring.