Disparity of race reporting in US Food and Drug Administration drug approvals for urinary system cancers from 2006 to 2021

被引:3
|
作者
Glover, Michael [1 ]
Hui, Gavin [1 ]
Chiang, Ryan [1 ]
Savage, Philip [2 ]
Krell, Jonathan [3 ]
Julve, Maximilian [3 ]
Grivas, Petros [4 ]
Lythgoe, Mark [3 ]
Khaki, Ali Raza [5 ]
机构
[1] Stanford Univ, Dept Med, Stanford, CA 94305 USA
[2] Brighton & Sussex Univ Hosp NHS Trust, Dept Oncol, Brighton, E Sussex, England
[3] Hammersmith Hosp, Imperial Coll London, Dept Surg & Canc, London, England
[4] Univ Washington, Fred Hutchinson Canc Res Ctr, Dept Med, Div Med Oncol,Clin Res Div, Seattle, WA USA
[5] Stanford Univ, Dept Med, Div Oncol, Stanford, CA USA
关键词
D O I
10.1111/bju.15629
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:168 / 170
页数:3
相关论文
共 50 条
  • [31] Monitoring adverse drug events: The Food and Drug Administration MedWatch reporting system
    Landow, L
    REGIONAL ANESTHESIA AND PAIN MEDICINE, 1998, 23 (06): : 190 - 193
  • [32] Reporting of immune-related adverse events (irAEs) in US Food and Drug Administration (FDA) approvals of immune checkpoint inhibitors
    Tapiavala, Shaili
    Shenouda, Mina A.
    Patel, Vaibhav G.
    Davis, Andrew A.
    JOURNAL OF CLINICAL ONCOLOGY, 2024, 42 (16)
  • [33] Psoriasis adverse events and associated medications as reported in the US Food and Drug Reporting System from 2016 to 2021
    Learned, Christine
    Alsukait, Sara
    Deverapalli, Sandhya
    Elliott, Erika
    Moody, Katherine
    Sobell, Jeffrey
    Konnikov, Nellie
    Ortega, Melissa
    Rosmarin, David
    JAAD INTERNATIONAL, 2022, 7 : 144 - 145
  • [34] Assessing drug lag in new drug approvals by the Iran Food and Drug Administration compared to the US FDA, EMA, and PMDA: A 20-year analysis (2001-2021)
    Alipour, Sama
    Parashkouhi, Sadra Nadimi
    Mojahedian, Mohammadmahdi
    Abbasian, Hadi
    MEDICINE, 2024, 103 (25)
  • [35] Improving Manufacturer Reporting of Adverse Events to the US Food and Drug Administration
    Redberg, Rita F.
    JAMA INTERNAL MEDICINE, 2015, 175 (09) : 1566 - 1567
  • [36] An assessment of drug-induced rhabdomyolysis cases within the US Food and Drug Administration Adverse Event Reporting System
    Bin Dayel, Faten
    Alfirevic, Ana
    Turner, Richard
    Chadwick, Amy
    BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2021, 87 (03) : 1617 - 1618
  • [37] Analysis of Information on Drug Adverse Reactions Using US Food and Drug Administration Adverse Event Reporting System (FAERS)
    Nango, Daisuke
    Sekizuka, Tuyoshi
    Goto, Makoto
    Echizen, Hirotoshi
    YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, 2022, 142 (04): : 341 - 344
  • [38] Performance of subgrouped proportional reporting ratios in the US food and drug administration (FDA) adverse event reporting system
    Dauner, Dan
    Zhang, Rui
    Adam, Terrence
    Leal, Eleazar
    Farley, Joel F.
    PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2022, 31 : 598 - 598
  • [39] Empirical estimation of under-reporting in the US Food and Drug Administration Adverse Event Reporting System (FAERS)
    Alatawi, Yasser M.
    Hansen, Richard A.
    EXPERT OPINION ON DRUG SAFETY, 2017, 16 (07) : 761 - 767
  • [40] Performance of subgrouped proportional reporting ratios in the US Food and Drug Administration (FDA) adverse event reporting system
    Dauner, Daniel G.
    Zhang, Rui
    Adam, Terrence J.
    Leal, Eleazar
    Heitlage, Viviene
    Farley, Joel F.
    EXPERT OPINION ON DRUG SAFETY, 2023, 22 (07) : 589 - 597