The Changing Face of Drug-induced Adrenal Insufficiency in the Food and Drug Administration Adverse Event Reporting System

被引:11
|
作者
Raschi, Emanuel [1 ]
Fusaroli, Michele [1 ]
Massari, Francesco [2 ]
Mollica, Veronica [2 ]
Repaci, Andrea [3 ]
Ardizzoni, Andrea [2 ,4 ]
Poluzzi, Elisabetta [1 ]
Pagotto, Uberto [3 ,5 ]
Di Dalmazi, Guido [3 ,5 ]
机构
[1] Univ Bologna, Dept Med & Surg Sci, Pharmacol Unit, Alma Mater Studiorum, I-40138 Bologna, Italy
[2] IRCCS Azienda Osped Univ Bologna, Med Oncol Unit, I-40138 Bologna, Italy
[3] IRCCS Azienda Osped Univ Bologna, Div Endocrinol & Diabet Prevent & Care Unit, I-40138 Bologna, Italy
[4] Univ Bologna, Dept Expt Diagnost & Specialty Med, Alma Mater Studiorum, Policlin S Orsola Malpighi, I-40138 Bologna, Italy
[5] Univ Bologna, Dept Med & Surg Sci DIMEC, Alma Mater Studiorum, I-40138 Bologna, Italy
来源
关键词
adrenal insufficiency; drug-induced; iatrogenic; glucocorticoid; withdrawal; checkpoint; immune checkpoint inhibitors; cancer; FDA; FAERS; CUSHINGS-SYNDROME; MANAGEMENT; INHIBITORS;
D O I
10.1210/clinem/dgac359
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Adrenal insufficiency (AI) is a life-threatening condition complicating heterogeneous disorders across various disciplines, with challenging diagnosis and a notable drug-induced component. Objective This work aimed to describe the spectrum of drug-induced AI through adverse drug event reports received by the US Food and Drug Administration (FDA). Methods A retrospective disproportionality analysis reporting trends of drug-induced AI was conducted on the FDA Adverse Event Reporting System (FAERS) (> 15 000 000 reports since 2004). AE reports were extracted from FAERS over the past 2 decades. Interventions included cases containing any of the preferred terms in the Medical Dictionary for Regulatory Activities describing AI, and signals of disproportionate reporting for drugs recorded in 10 or more cases as primary suspect. Results We identified 8496 cases of AI: 97.5% serious, 41.1% requiring hospitalization. AI showed an exponential increase throughout the years, with 5282 (62.2%) cases in 2015 to 2020. We identified 56 compounds associated with substantial disproportionality: glucocorticoids (N = 1971), monoclonal antibodies (N = 1644, of which N = 1330 were associated with immune checkpoint inhibitors-ICIs), hormone therapy (N = 291), anti-infectives (N = 252), drugs for hypercortisolism or adrenocortical cancer diagnosis/treatment (N = 169), and protein kinase inhibitors (N = 138). Cases of AI by glucocorticoids were stable in each 5-year period (22%-27%), whereas those by monoclonal antibodies, largely ICIs, peaked from 13% in 2010 to 2015 to 33% in 2015 to 2020. Conclusion We provide a comprehensive insight into the evolution of drug-induced AI, highlighting the heterogeneous spectrum of culprit drug classes and the emerging increased reporting of ICIs. We claim for the urgent identification of predictive factors for drug-induced AI, and the establishment of screening and educational protocols for patients and caregivers.
引用
收藏
页码:E3107 / E3114
页数:8
相关论文
共 50 条
  • [21] Pharmacovigilance study of famciclovir in the Food and Drug administration adverse event reporting system database
    Fang, Runan
    Zhou, Yang
    Han, Lu
    Chen, Wenjing
    Guan, Ning
    Li, Jianhong
    SCIENTIFIC REPORTS, 2024, 14 (01):
  • [22] Complementing the US Food and Drug Administration Adverse Event Reporting System With Adverse Drug Reaction Reporting From Social Media: Comparative Analysis
    Zhou, Zeyun
    Hultgren, Kyle Emerson
    JMIR PUBLIC HEALTH AND SURVEILLANCE, 2020, 6 (03): : 144 - 155
  • [23] Newly identified adverse events of enzalutamide using the food and drug administration adverse event reporting system
    Wang, Xin
    Chang, Lina
    Li, Zhenhua
    Jiang, Yuanfang
    Chen, Yue
    Jia, Xinli
    Wang, Qiye
    Ren, Xiaolu
    Ma, Zhifang
    Zhang, Wei
    EXPERT OPINION ON DRUG SAFETY, 2023, 22 (11) : 1099 - 1103
  • [24] Intestinal Adverse Outcomes With Pancreatic Enzymes: An Analysis of the Food and Drug Administration Adverse Event Reporting System
    Stobaugh, Derrick J.
    Deepak, Parakkal
    Ehrenpreis, Eli D.
    GASTROENTEROLOGY, 2013, 144 (05) : S457 - S457
  • [25] Pharmacovigilance analysis of drug-induced hypofibrinogenemia using the FDA Adverse Event Reporting System
    Wen, Xiao
    Cai, Le
    Gao, Ao
    Fu, An
    Guo, Daihong
    Zhu, Man
    INTERNATIONAL JOURNAL OF CLINICAL PHARMACY, 2025,
  • [26] Pediatric drug-induced anaphylaxis reports in the FDA Adverse Event Reporting System (FAERS)
    Brameli, Anna
    Yuan, Irene H.
    Phillips, Elizabeth J.
    Stone Jr, Cosby A.
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2024, 12 (09):
  • [27] A Pharmacovigilance Study of Drug-Induced Glaucoma Utilizing the Japanese Adverse Event Reporting System
    Kozaru, Mariko
    Iida, Tatsuya
    Hosohata, Keiko
    CLINICAL OPHTHALMOLOGY, 2023, 17 : 3645 - 3653
  • [28] Adverse event profiles after brand or generic clopidogrel in the Food and Drug Administration Adverse Event Reporting System (FAERS)
    Serebruany, V. L.
    Kim, M-H.
    EUROPEAN HEART JOURNAL, 2018, 39 : 437 - 437
  • [29] Monitoring adverse drug events: The Food and Drug Administration MedWatch reporting system
    Landow, L
    REGIONAL ANESTHESIA AND PAIN MEDICINE, 1998, 23 (06): : 190 - 193
  • [30] Annual adverse event profiles after clopidogrel, prasugrel, and ticagrelor in the Food and Drug Administration Adverse Event Reporting System
    Cherepanov, Vasily
    Fortmann, Seth D.
    Kim, Moo Hyun
    Marciniak, Thomas A.
    Litvinov, Oleg
    Mihalev, Kyryl
    Serebruany, Victor L.
    EUROPEAN HEART JOURNAL-CARDIOVASCULAR PHARMACOTHERAPY, 2018, 4 (02) : 69 - 71