Post-Marketing Assessment of Neuropsychiatric Adverse Events in Influenza Patients Treated with Oseltamivir: An Updated Review

被引:0
|
作者
Stephen Toovey
Eric P. Prinssen
Craig R. Rayner
Bharat T. Thakrar
Regina Dutkowski
Annette Koerner
Tom Chu
Alexandra Sirzen-Zelenskaya
Markus Britschgi
Sudhir Bansod
Barbara Donner
机构
[1] F. Hoffmann-La Roche Ltd.,
[2] Roche Products Pty. Ltd.,undefined
[3] Hoffmann-La Roche,undefined
[4] Inc.,undefined
来源
Advances in Therapy | 2012年 / 29卷
关键词
Adverse events; Central nervous system; Influenza; Neuropsychiatric; Oseltamivir; Safety; Tolerability;
D O I
暂无
中图分类号
学科分类号
摘要
A 2008 review by our group concluded that the risk of neuropsychiatric adverse events (NPAEs) in influenza patients was not increased by oseltamivir exposure, and did not identify any mechanism by which oseltamivir or its metabolites could cause or worsen such events. The current article reviews new information on this topic. Between September 16, 2007 and May 15, 2010, 1,805 spontaneously-reported NPAEs were identified in 1,330 patients receiving oseltamivir: 767 (42.5%) from Japan, 296 (16.4%) from the USA, and 742 (41.1%) from other countries. NPAEs were more common in children: 1,072 (59.4%) events were in those aged ≤16 years. NPAEs often occurred within 48 h of treatment initiation (953 events; 52.8%). Nearly half of the events were serious in nature (838; 46.4%). The three largest categories of events were abnormal behavior (457 events, 25.3%), miscellaneous psychiatric events (370; 20.5%), and delusions/perceptual disturbances (316 events, 17.5%). A total of 1,545 events (85.6%) in eight different categories were considered to be delirium or delirium-like. Twenty-eight suicide-related events were reported. A US healthcare claims database analysis showed that the risk of NPAEs in 7,798 oseltamivir-treated patients was no higher than that in 10,411 patients not on antivirals, but a study on oseltamivir and abnormal behavior in Japan was less conclusive. NPAE frequency in oseltamivir-exposed Japanese and Taiwanese children with influenza was the same as in unexposed children. New analysis of the UK General Practice Research Database showed that the relative adjusted risk of NPAEs in influenza patients was 2.18-times higher than in the general population. Other epidemiology studies report frequent occurrence of encephalitis and similar disorders in influenza patients independently of oseltamivir exposure. The new data support the findings of the original assessment. Evidence suggests that influenza-related encephalopathies are caused by influenza-induced inflammatory responses, but more work is needed to confirm the underlying mechanisms.
引用
收藏
页码:826 / 848
页数:22
相关论文
共 50 条
  • [41] TNF ANTAGONIST DRUG SAFETY ASSESSMENT BY PHARMACOVIGILANCE SIGNALING AND POST-MARKETING ADVERSE EVENT REPORTS
    Cavaco, M.
    Araujo, F.
    Eurico Fonseca, J.
    Goncalves, J.
    ANNALS OF THE RHEUMATIC DISEASES, 2017, 76 : 784 - 785
  • [42] Unveiling unexpected adverse events: post-marketing safety surveillance of gilteritinib and midostaurin from the FDA Adverse Event Reporting database
    Jiang, Tingting
    Li, Yanping
    Zhang, Ni
    Gan, Lanlan
    Su, Hui
    Xiang, Guiyuan
    Wu, Yuanlin
    Liu, Yao
    THERAPEUTIC ADVANCES IN DRUG SAFETY, 2025, 16
  • [43] Disproportionality analysis of adverse events associated with asfotase alfa: a post-marketing study using the FDA Adverse Event Reporting System
    Wang, Wen
    Wang, Zhe
    Chen, Qianxiu
    Sun, Haixia
    Fu, Zongchao
    Han, Jing
    Lv, Hao
    EXPERT OPINION ON DRUG SAFETY, 2024,
  • [44] Characterization of Patients with Rheumatoid Arthritis Treated with Rituximab or Tocilizumab in Post-Marketing Patient Registries
    Tatt, Iain D.
    Sarsour, Khaled
    Robinson, Jamie
    Low, Eric
    Napalkov, Pavel
    PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2013, 22 : 440 - 441
  • [45] Safety of Sublingual Immunotherapy: A Secondary Analysis of Post-marketing Adverse Events Reports Using a Japanese Public Database
    Kaneda, Yudai
    Kaneda, Uiri
    Namba, Mira
    Tanimoto, Tetsuya
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2023, 15 (09)
  • [46] POST-MARKETING ADVERSE EVENTS OF ONCOLOGY MEDICATIONS WITH BREAKTHROUGH THERAPY DESIGNATION CORRELATED WITH TIME ON MARKET AND MARKET SHARE
    Heitlage, V
    Farley, J. F.
    Shah, R.
    Tyagi, H.
    Stenehjem, D.
    VALUE IN HEALTH, 2022, 25 (07) : S460 - S460
  • [47] Assessment of Tumor Lysis Syndrome in Patients with Chronic Lymphocytic Leukemia Treated with Venetoclax in the Clinical Trial and Post-Marketing Settings
    Seymour, John F.
    Gribben, John G.
    Davids, Matthew S.
    Mato, Anthony
    Sharman, Jeff P.
    Cyr, Aimee
    Bartkus, Cynthia
    Pena, German
    Boyer, Michelle
    Sharmokh, Simon
    Rosenberg, Tanya S.
    Wierda, William G.
    BLOOD, 2020, 136
  • [48] PREDICTORS OF ADVERSE EVENTS FOLLOWING X-TACK USE: A CASE CONTROL ANALYSIS OF A POST-MARKETING REGISTRY
    Sayegh, Lea
    Salameh, Yara
    Buttar, Navtej
    Song, Louis Wong Kee
    Chandrasekhara, Vinay
    Abu Dayyeh, Barham
    Storm, Andrew
    GASTROINTESTINAL ENDOSCOPY, 2024, 99 (06) : AB265 - AB265
  • [49] A prospective post-marketing survey of the clinical use of pregabalin: A reliable tool to detect rare or late adverse events
    Pollard, John R.
    Herman, Susan T.
    Litt, Brian
    Krieger, Ruth S.
    French, Jacqueline A.
    EPILEPSIA, 2006, 47 : 170 - 170
  • [50] Allergic adverse events following immunization: Data from post-marketing surveillance in Apulia region (South of Italy)
    Stefanizzi, Pasquale
    Ferorelli, Davide
    Scazzi, Francesco Livio
    Di Lorenzo, Antonio
    Martinelli, Andrea
    Trinchera, Chiara
    Moscara, Lorenza
    Miniello, Enrico
    Di Bona, Danilo
    Tafuri, Silvio
    FRONTIERS IN IMMUNOLOGY, 2023, 14