Harms are assessed inconsistently and reported inadequately part 1: systematic adverse events

Author:

Mayo-Wilson EvanORCID,Fusco Nicole,Li Tianjing,Hong Hwanhee,Canner Joseph K.,Dickersin Kay,Bertizzolo Lorenzo,Cowley Terrie,Doshi Peter,Ehmsen Jeffrey,Gresham Gillian,Guo Nan,Haythornthwaite Jennifer,Heyward James,Pham Diana,Payne Jennifer,Rosman Lori,Stuart Elizabeth,Suarez-Cuervo Catalina,Tolbert Elizabeth,Twose Claire,Vedula Swaroop

Publisher

Elsevier BV

Subject

Epidemiology

Reference27 articles.

1. CFR Title 21, Section 312,2010

2. Harms are assessed inconsistently and reported inadequately Part 2: non-systematic adverse events;Mayo-Wilson;J Clin Epidemiol,2019

3. Recommendations to improve adverse event reporting in clinical trial publications: a joint pharmaceutical industry/journal editor perspective;Lineberry;BMJ,2016

4. Cherry-picking by trialists and meta-analysts can drive conclusions about intervention efficacy;Mayo-Wilson;J Clin Epidemiol,2017

5. Caveat emptor: the combined effects of multiplicity and selective reporting;Li;Trials,2018

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