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serious adverse event

40 papers and 10 presentations; 49 titles.

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Conference × Year × Title × Authors Extras Pages
PharmaSUG CN 2026 Safety Estimands and Analysis Dataset Design: Advancing Safety Evaluation in Clinical Trials Kun Ren,
Zeyu Guang		 source 11
PharmaSUG 2026 Two Approaches to Phase-Specific TRTEMFL in ADAE: A Neoadjuvant-Adjuvant Case with Surgery Between Phases Youlan Shen,
Leah Suttner		 source 6
PHUSE EU 2025 Hybrid Way To Develop Patient Narratives [presentation] Loskutov Volodymyr,
Oleh Buno		 source 16
PharmaSUG 2025 Automating Recurring Data Reconciliation for Serious Adverse Events Using SAS Patrick Dowe,
Gina Hird		 source 25
PHUSE US 2025 Enhancing Clinical Trial Data Queries with LLMs and Neo4j: A Flexible Framework for ADaM Dataset Management Jaime Yan source
presentation source		 28
PharmaSUG 2024 Safety Signals from Patient Narratives PLUS: Augmenting Artificial Intelligence to Enhance Generative AI Value Sherrine Eid,
Sundaresh Sankaran		 source 14
PHUSE US 2024 A SAS Tool for Generating Adverse Event Summaries in XML Format Using ADaM Datasets ADSL and ADAE for ClinicalTrial.gov and EudraCT Submissions [presentation] Karthika Bhavadas,
Shabeeb Kannattikuni		 source 23
PHUSE EU 2023 Development Safety Update Report (DSUR)/Periodic Safety Update Report (PSUR) Phillip Spowart source
presentation source		 8
PharmaSUG 2023 Bringing it All Together: Applying the Analytics Life Cycle for Natural Language Processing to Life Sciences Sundaresh Sankaran,
Tom Sabo		 source 15
PharmaSUG 2023 Programmer-s Perspective: Step into Awareness Regarding Clinical Trial Deliverables and Their Impact Lyma Faroz,
Jinit Mistry		 source 10
PharmaSUG 2022 A Practical Approach to Preparing Documentation for Clinical Registries Jennifer McGrogan,
Rex Tungala,
Mario Widel		 source 16
PharmaSUG 2022 Avoid Common Mistakes in Preparing the BIMO Deliverables Chintan Pandya,
Himanshu Patel		 source 9
PHUSE US 2022 The Emerging Use of Automation to Address the Challenge of Cross-Table Consistency Checking of Output Used in the Reporting of Clinical Trial Data [presentation] Hugh Donovan,
Naama Feilchenfeld		 source
video		 16
PHUSE US 2021 Automate Scientific Document such as CSR Generation using ML/NLP [presentation] Farha Feroze source
video		 13
PHUSE US 2021 Automated Validation of Clinical Trial Analysis and Reporting Deliverables Using 'testthat' [presentation] Amin Shirazi,
Jane X. Liao		 source
video		 35
PHUSE US 2021 CSR Narratives Automation [presentation] Ritesh Dhimmar source
video		 23
PHUSE US 2021 Do EudraCT the Easy Way: Semi-automation of Inputting Study & Treatment Event Information in EudraCT [presentation] Kevin Miller,
Larry Sleeper		 source
video		 21
PHUSE US 2021 Visually-enhanced Patient Narrative [poster] Abhinav Srivastva source 1
PharmaSUG 2020 Programming Patient Narratives Using Microsoft Word XML files Yuping Wu,
Jan Skowronski		 source 9
PHUSE US 2020 Adverse Event and Treatment Emergent Approaches in the Industry Aimee Basile source
poster source		 11
PHUSE EU 2019 Semi Auto-generated Narratives Bjarke Klein source
presentation source		 7
PHUSE US 2018 Adverse Event Analysis - One step forward! Anuja Rasal source
presentation source		 11
PHUSE US 2018 Modeling and Text Analysis to Empower FAERS Adverse Event Mitigation Qais Hatim,
Emily McRae		 source
presentation source		 24
PharmaSUG 2018 Graph Display of Patient Profile in SAS Yanwei Han source 7
PHUSE EU 2017 Assessing New CFDA Requirements on Data Integrity Using Risk-Based Monitoring and Enrollment Patterns Wenjun Bao,
Richard C. Zink,
Geoffrey A. Mann		 source
presentation source		 13
MWSUG 2017 Patient Safety with SAS Visual Analytics Piyush K. Singh,
Prasoon Sangwan,
Ghiyasuddin Mohammed Faraz Khan		 12
PHUSE EU 2016 Standard Safety Visualisation Set-up Using Spotfire Michaela Mertes source
presentation source		 10
MWSUG 2016 Pre-Data Checks for SDTM Development Abhinav Srivastva 10
PharmaSUG 2016 Efficient Safety Assessment in Clinical Trials using the Computer-generated AE Narratives of JMP Clinical Richard C. Zink,
Drew Foglia		 source 13
PHUSE EU 2014 Successfully Embracing Challenges to CDISC Standards [presentation] Elke Sennewald source 30
PharmaSUG 2014 Risk-Based Approach to Identifying and Selecting Clinical Sites for Sponsor's Preparation for FDA/EMA Inspection Xiangchen (Bob) Cui source 21
PHUSE EU 2013 EXACT - A Metadata Driven System for Creating Standard Mockups and Data Displays [presentation] Kent Letourneau source 55
PharmaSUG 2013 JMP versus JMP Clinical for Interactive Visualization of Clinical Trials Data Doug Robinson,
Jordan Hiller		 source 11
MWSUG 2012 Programmed Assisted Patient Narratives (PANs) with New SAS ODS and Graphical Approaches Faye Yeh,
Melvin S. Munsaka		 12
PharmaSUG 2012 Experience of Generating an XML file and Uploading Serious and Frequent Adverse Events to ClinicalTrials.gov Juan Wu,
Min Lai		 source 9
PharmaSUG 2012 Supplementing Programmed Assisted Patient Narratives (PANs) with Graphs Using SAS Faye Yeh,
Melvin S. Munsaka		 source 12
SESUG 2011 Resolving OpenCDISC Error Messages Using SAS John R. Gerlach source 11
PharmaSUG 2011 Resolving OpenCDISC Error Messages Using SAS Virginia Redner,
John R. Gerlach		 source 10
PharmaSUG 2011 Validating Controlled Terminology in SDTM Domains John R. Gerlach source 12
PHUSE EU 2010 Electronic transfer of sAE to Global Pharmacovigilance Eva Bervar source
presentation source		 5
PharmaSUG 2010 The Compliance and Implementation of Clinical Trial Outcome Disclosure on ClinicalTrials.gov Eric T. Sun,
Craig Anderson		 13
PHUSE EU 2009 ClinicalTrials.gov - a programmers perspective Ralf Minkenberg source
presentation source		 6
PharmaSUG 2007 An Application of ODS Tagset to Produce HTML Files for Clinical Study Reports Li Luo 10
PharmaSUG 2005 Selected SAS Macro and SQL Techniques For Efficient Analysis Programming Brian P. Fairfield-Carter 12
SUGI 2005 CALL EXECUTE: A Powerful Data Management Tool Denis Michel source 13
NESUG 2000 Programming Data Displays Using SAS Software: Meeting Regulatory Requirements for Quality Michael A. Walega 11
PharmaSUG 2000 Using the Annotate Facility for Enhancing Output Marcia Branham,
Timothy Maxwell		 7
MWSUG 1999 PROC SQL Dictionary Tables - A Great Source of Information about Data Sets Wendih S. Yao 4
PharmaSUG 1998 Identifying and Reporting of Medically Serious Adverse Events: An Interactive Approach Anna Kunina,
Palo Alto		 3
PharmaSUG 1998 PROC SQL Dictionary Tables - A Great Source of Information about Data Sets Wendih S. Yao 4

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