Search results: Sage Journals

Open accessResearch articleFirst published April, 2024

Risk Factors of Serious Adverse Events for Geriatric Hip Fractures: Is it the Frailty or the Timing?

Ling-xiao Wang, Li-juan Guan, Ming-hong Deng [...]

Geriatric Orthopaedic Surgery & Rehabilitation

Open accessResearch articleFirst published 2025

Automatic tool for the reconciliation of serious adverse events for pharmacovigilance: design and implementation of Reconciliaid

Sara Contu, Renaud Schiappa, Yann Chateau [...]

Therapeutic Advances in Drug Safety

Restricted accessResearch articleFirst published July, 2014

A Bayesian Stopping Rule for Sequential Monitoring of Serious Adverse Events

Kosuke Kashiwabara, Yutaka Matsuyama, Yasuo Ohashi

Therapeutic Innovation & Regulatory Science

Restricted accessOtherFirst published May, 2009

Early Stopping Rules in Clinical Trials Based on Sequential Monitoring of Serious Adverse Events

A. Kramar, C. Bascoul-Mollevi

Medical Decision Making

Restricted accessResearch articleFirst published May, 2018

Comparison of Serious Adverse Event Profiles Among Antirheumatic Agents Using Japanese Adverse Drug Event Report Database

Yomei Matsuoka, Mamoru Narukawa

Therapeutic Innovation & Regulatory Science

Restricted accessResearch articleFirst published December, 2020

Evaluation of Serious Adverse Event Reporting Forms for Clinical Trials: A Comparative Korean Study

Heeyoung Lee, Cholong Park, Jinwon Choi [...]

Journal of Empirical Research on Human Research Ethics

Restricted accessResearch articleFirst published July, 2016

Serious Adverse Events Reports

Raakhi K. Tripathi, Padmaja A. Marathe, Sandip V. Kapse [...]

Journal of Empirical Research on Human Research Ethics

Restricted accessResearch articleFirst published October, 2009

The automation of clinical trial serious adverse event reporting workflow

Jack W London, Karl J Smalley, Kyle Conner [...]

Clinical Trials

Free accessResearch articleFirst published January, 2014

Triptans and serious adverse vascular events: Data mining of the FDA Adverse Event Reporting System database

Giuseppe Roberto, Carlo Piccinni, Roberto D’Alessandro [...]

Cephalalgia

Restricted accessOtherFirst published October, 2001

A Surveillance Program for Serious Adverse Events during Phase III Drug Development Studies

Philip Hougaard

Therapeutic Innovation & Regulatory Science

Open accessResearch articleFirst published April, 2024

Risk Factors of Serious Adverse Events for Geriatric Hip Fractures: Is it the Frailty or the Timing?

Ling-xiao Wang, Li-juan Guan, Ming-hong Deng [...]

Geriatric Orthopaedic Surgery & Rehabilitation

Open accessResearch articleFirst published 2025

Automatic tool for the reconciliation of serious adverse events for pharmacovigilance: design and implementation of Reconciliaid

Sara Contu, Renaud Schiappa, Yann Chateau [...]

Therapeutic Advances in Drug Safety

Restricted accessResearch articleFirst published July, 2014

A Bayesian Stopping Rule for Sequential Monitoring of Serious Adverse Events

Kosuke Kashiwabara, Yutaka Matsuyama, Yasuo Ohashi

Therapeutic Innovation & Regulatory Science

Restricted accessOtherFirst published May, 2009

Early Stopping Rules in Clinical Trials Based on Sequential Monitoring of Serious Adverse Events

A. Kramar, C. Bascoul-Mollevi

Medical Decision Making

Restricted accessResearch articleFirst published May, 2018

Comparison of Serious Adverse Event Profiles Among Antirheumatic Agents Using Japanese Adverse Drug Event Report Database

Yomei Matsuoka, Mamoru Narukawa

Therapeutic Innovation & Regulatory Science

Restricted accessResearch articleFirst published December, 2020

Evaluation of Serious Adverse Event Reporting Forms for Clinical Trials: A Comparative Korean Study

Heeyoung Lee, Cholong Park, Jinwon Choi [...]

Journal of Empirical Research on Human Research Ethics

Restricted accessResearch articleFirst published July, 2016

Serious Adverse Events Reports

Raakhi K. Tripathi, Padmaja A. Marathe, Sandip V. Kapse [...]

Journal of Empirical Research on Human Research Ethics

Restricted accessResearch articleFirst published October, 2009

The automation of clinical trial serious adverse event reporting workflow

Jack W London, Karl J Smalley, Kyle Conner [...]

Clinical Trials

Free accessResearch articleFirst published January, 2014

Triptans and serious adverse vascular events: Data mining of the FDA Adverse Event Reporting System database

Giuseppe Roberto, Carlo Piccinni, Roberto D’Alessandro [...]

Cephalalgia

Restricted accessOtherFirst published October, 2001

A Surveillance Program for Serious Adverse Events during Phase III Drug Development Studies

Philip Hougaard

Therapeutic Innovation & Regulatory Science