Skip to main content
Journal ArticleOPEN ACCESS

Adverse Event Reporting in Clinical Trials: Time to Include Duration as Well as Severity

  • Sartor O
The Oncologist (2018) 23(1) 1-1
DOI: 10.1634/theoncologist.2017-0437
16Citations
Citations of this article
19Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

This editorial discusses flaws in the current system for reporting adverse events.

Cite

CITATION STYLE

APA

Sartor, O. (2018). Adverse Event Reporting in Clinical Trials: Time to Include Duration as Well as Severity. The Oncologist, 23(1), 1–1. https://doi.org/10.1634/theoncologist.2017-0437

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free