Novel Adverse Events of Iloperidone: A Disproportionality Analysis in US Food and Drug Administration Adverse Event Reporting System (FAERS) Database

被引:34
|
作者
Subeesh, Viswam [1 ]
Maheswari, Eswaran [1 ]
Singh, Hemendra [2 ]
Beulah, Thomas Elsa [1 ]
Swaroop, Ann Mary [1 ]
机构
[1] MS Ramaiah Univ Appl Sci, Dept Pharm Practice, Fac Pharm, Bengaluru, India
[2] Ramaiah Med Coll, Dept Psychiat, Bengaluru, India
关键词
Pharmacovigilance; disproportionality analysis; reporting odds ratio; iloperidone; drug safety; FAERS; SCHIZOPHRENIA; ANTIPSYCHOTICS; SAFETY; CARE;
D O I
10.2174/1574886313666181026100000
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: The signal is defined as "reported information on a possible causal relationship between an adverse event and a drug, of which the relationship is unknown or incompletely documented previously". Objective: To detect novel adverse events of iloperidone by disproportionality analysis in FDA database of Adverse Event Reporting System (FAERS) using Data Mining Algorithms (DMAs). Methodology: The US FAERS database consists of 1028 iloperidone associated Drug Event Combinations (DECs) which were reported from 2010 Q1 to 2016 Q3. We consider DECs for disproportionality analysis only if a minimum of ten reports are present in database for the given adverse event and which were not detected earlier (in clinical trials). Two data mining algorithms, namely, Reporting Odds Ratio (ROR) and Information Component (IC) were applied retrospectively in the aforementioned time period. A value of ROR-1.96SE>1 and IC-2SD>0 were considered as the threshold for positive signal. Results: The mean age of the patients of iloperidone associated events was found to be 44years [95% CI: 36-51], nevertheless age was not mentioned in twenty-one reports. The data mining algorithms exhibited positive signal for akathisia (ROR-1.96SE=43.15, IC-2SD=2.99), dyskinesia (21.24, 3.06), peripheral oedema (6.67, 1.08), priapism (425.7, 9.09) and sexual dysfunction (26.6-1.5) upon analysis as those were well above the pre-set threshold. Conclusion: Iloperidone associated five potential signals were generated by data mining in the FDA AERS database. The result requires an integration of further clinical surveillance for the quantification and validation of possible risks for the adverse events reported of iloperidone.
引用
收藏
页码:21 / 26
页数:6
相关论文
共 50 条
  • [31] Spontaneous Reporting on Adverse Events by Consumers in the United States: An Analysis of the Food and Drug Administration Adverse Event Reporting System Database
    Toki T.
    Ono S.
    [J]. Drugs - Real World Outcomes, 2018, 5 (2) : 117 - 128
  • [32] Newer Antiseizure Medications and Suicidality: Analysis of the Food and Drug Administration Adverse Event Reporting System (FAERS) Database
    Leppien, Emily E.
    Doughty, Bennett J.
    Hurd, Karyssa L.
    Strong, Keira N.
    Piper, Brian J.
    McCall, Kenneth L.
    [J]. CLINICAL DRUG INVESTIGATION, 2023, 43 (06) : 393 - 399
  • [33] Comparison of brand versus generic antiepileptic drug adverse event reporting rates in the US Food and Drug Administration Adverse Event Reporting System (FAERS)
    Rahman, Md. Motiur
    Alatawi, Yasser
    Cheng, Ning
    Qian, Jingjing
    Plotkina, Annya V.
    Peissig, Peggy L.
    Berg, Richard L.
    Page, David
    Hansen, Richard A.
    [J]. EPILEPSY RESEARCH, 2017, 135 : 71 - 78
  • [34] NOVEL ADVERSE EVENTS OF CGRP RECEPTOR ANTAGONISTS: A DISPROPORTIONALITY ANALYSIS IN USFDA ADVERSE EVENT REPORTING SYSTEM DATABASE
    Sangnure, A.
    Das, A.
    Sajjan, S.
    Ac, R.
    [J]. VALUE IN HEALTH, 2023, 26 (06) : S372 - S373
  • [35] Investigating bleeding adverse events associated with BTK inhibitors in the food and drug administration adverse event reporting system (FAERS)
    Li, Xianlin
    Shang, Nan
    Yan, Qianci
    Yue, Xiunan
    Liu, Yang
    Zheng, Xiaojun
    [J]. EXPERT OPINION ON DRUG SAFETY, 2024,
  • [36] Comparisons of adverse event reporting for colistin versus polymyxin B using the US Food and Drug Administration Adverse Event Reporting System (FAERS)
    Cong Bang Truong
    Durham, Spencer H.
    Qian, Jingjing
    [J]. EXPERT OPINION ON DRUG SAFETY, 2021, 20 (05) : 603 - 609
  • [37] Amyotrophic Lateral Sclerosis as an Adverse Drug Reaction: A Disproportionality Analysis of the Food and Drug Administration Adverse Event Reporting System
    Gaimari, Anna
    Fusaroli, Michele
    Raschi, Emanuel
    Baldin, Elisa
    Vignatelli, Luca
    Nonino, Francesco
    De Ponti, Fabrizio
    Mandrioli, Jessica
    Poluzzi, Elisabetta
    [J]. DRUG SAFETY, 2022, 45 (06) : 663 - 673
  • [38] Amyotrophic Lateral Sclerosis as an Adverse Drug Reaction: A Disproportionality Analysis of the Food and Drug Administration Adverse Event Reporting System
    Anna Gaimari
    Michele Fusaroli
    Emanuel Raschi
    Elisa Baldin
    Luca Vignatelli
    Francesco Nonino
    Fabrizio De Ponti
    Jessica Mandrioli
    Elisabetta Poluzzi
    [J]. Drug Safety, 2022, 45 : 663 - 673
  • [39] Empirical estimation of under-reporting in the US Food and Drug Administration Adverse Event Reporting System (FAERS)
    Alatawi, Yasser M.
    Hansen, Richard A.
    [J]. EXPERT OPINION ON DRUG SAFETY, 2017, 16 (07) : 761 - 767
  • [40] A disproportionality analysis of sunitinib in the FDA adverse event reporting system (FAERS)
    Zou, Wenbin
    Yang, Han
    Xi, Yu
    Zeng, Chenxi
    Chen, Wei
    Fu, Xiangning
    [J]. HELIYON, 2024, 10 (17)