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Drug Safety|July 10, 2014
Advancing the field of pharmaceutical risk minimization through application of implementation science best practicesMeredith Y Smith, Elaine MorratoDrug Safety|October 5, 2013
Patient-Reported Outcome Measures in Safety Event Reporting: PROSPER Consortium guidanceAnjan K Banerjee, Sally Okun, I Ralph Edwards, et al.Drug Safety|October 1, 2013
Adverse event reporting patterns of newly approved drugs in the USA in 2006: an analysis of FDA Adverse Event Reporting System dataPankdeep Chhabra, Xing Chen, Sheila R WeissDrug Safety|October 30, 2013
Desideratum for evidence based epidemiologyJ Marc Overhage, Patrick B Ryan, Martijn J Schuemie, et al.Drug Safety|October 30, 2013
Variation in choice of study design: findings from the Epidemiology Design Decision Inventory and Evaluation (EDDIE) surveyPaul E Stang, Patrick B Ryan, J Marc Overhage, et al.Drug Safety|October 30, 2013
Empirical performance of a new user cohort method: lessons for developing a risk identification and analysis systemPatrick B Ryan, Martijn J Schuemie, Susan Gruber, et al.Drug Safety|October 30, 2013
Evaluation of disproportionality safety signaling applied to healthcare databasesWilliam DuMouchel, Patrick B Ryan, Martijn J Schuemie, et al.Drug Safety|October 30, 2013
Alternative outcome definitions and their effect on the performance of methods for observational outcome studiesChristian G Reich, Patrick B Ryan, Martijn J SchuemieDrug Safety|October 30, 2014
Methodology to assess clinical liver safety dataMichael Merz, Kwan R Lee, Gerd A Kullak-Ublick, et al.Drug Safety|March 24, 2026
US Risk Evaluation and Mitigation Strategies with Elements to Assure Safe Use: A Longitudinal Analysis of REMS Modifications (2008-2022)Elaine H Morrato, Elizabeth J Campagna, Cynthia LaCivita, et al.Pageof 310