An automated Serious Adverse Event reporting system

被引：0
|
作者：
Lawlor, S [1 ]
Cai, Y [1 ]
Kelley, S [1 ]
Belle, S [1 ]
机构：
[1] Univ Pittsburgh, Pittsburgh, PA 15260 USA
来源：
CONTROLLED CLINICAL TRIALS | 2003年 / 24卷
关键词：
D O I：
暂无
中图分类号：
R-3 [医学研究方法]; R3 [基础医学];
学科分类号：
1001 ;
摘要：
8
引用
收藏
页码：46S / 47S
页数：2
相关论文
共 50 条
  • [1] Serious Adverse Event Reporting
    Stewart, William C.
    Stewart, Jeanette A.
    Demos, Christina M.
    Turner, Meredith
    [J]. OPHTHALMOLOGY, 2009, 116 (12) : 2485 - 2486
  • [2] Serious Adverse Event Reporting in a Medical Device Information System
    Pecoraro, Fabrizio
    Luzi, Daniela
    [J]. USER CENTRED NETWORKED HEALTH CARE, 2011, 169 : 834 - 838
  • [3] Validation of Serious Adverse Event Reporting in a Multicenter Registry
    Basiaga, Matthew
    Pooni, Rajdeep
    Pinotti, Caitlan
    Buckley, Lisa
    Taxter, Alysha
    [J]. ARTHRITIS & RHEUMATOLOGY, 2023, 75 : 194 - 195
  • [4] Adverse event reporting: serious AEs coded as nonserious
    [J]. Reactions Weekly, 2016, 1586 (1) : 1 - 1
  • [5] Triptans and serious adverse vascular events: Data mining of the FDA Adverse Event Reporting System database
    Roberto, Giuseppe
    Piccinni, Carlo
    D'Alessandro, Roberto
    Poluzzi, Elisabetta
    [J]. CEPHALALGIA, 2014, 34 (01) : 5 - 13
  • [6] Serious adverse events with tedizolid and linezolid: pharmacovigilance insights through the FDA adverse event reporting system
    Gatti, Milo
    Fusaroli, Michele
    Raschi, Emanuel
    Moretti, Ugo
    Poluzzi, Elisabetta
    De Ponti, Fabrizio
    [J]. EXPERT OPINION ON DRUG SAFETY, 2021, 20 (11) : 1421 - 1431
  • [7] Introduction of a Mobile Adverse Event Reporting System Is Associated With Participation in Adverse Event Reporting
    Rubin, Daniel S.
    Pesyna, Colin
    Jakubczyk, Sharon
    Liao, Chuanhong
    Tung, Avery
    [J]. AMERICAN JOURNAL OF MEDICAL QUALITY, 2019, 34 (01) : 30 - 35
  • [8] The automation of clinical trial serious adverse event reporting workflow
    London, Jack W.
    Smalley, Karl J.
    Conner, Kyle
    Smith, J. Bruce
    [J]. CLINICAL TRIALS, 2009, 6 (05) : 446 - 454
  • [9] Serious Cardiovascular Adverse Events Reported with Intravenous Sedatives: A Retrospective Analysis of the MedWatch Adverse Event Reporting System
    Matthew S. Duprey
    Nada S. Al-Qadheeb
    Nick O’Donnell
    Keith B. Hoffman
    Jonathan Weinstock
    Christopher Madias
    Mo Dimbil
    John W. Devlin
    [J]. Drugs - Real World Outcomes, 2019, 6 : 141 - 149
  • [10] Serious Cardiovascular Adverse Events Reported with Intravenous Sedatives: A Retrospective Analysis of the MedWatch Adverse Event Reporting System
    Duprey, Matthew S.
    Al-Qadheeb, Nada S.
    O'Donnell, Nick
    Hoffman, Keith B.
    Weinstock, Jonathan
    Madias, Christopher
    Dimbil, Mo
    Devlin, John W.
    [J]. DRUGS-REAL WORLD OUTCOMES, 2019, 6 (03) : 141 - 149
12345