Central Nervous System Adverse Reactions to Amantadine Intoxication: A Case Report and Analysis of JADER.

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL In vivo Pub Date : 2024-07-01 DOI:10.21873/invivo.13669
Naohito Ide, Yui Hosoya, Mariko Yamamoto, Ayami Shigeno, Masakazu Obayashi, Kei Asada, Satoru Matsushima
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Abstract

Background/aim: A few case reports of central nervous system (CNS) symptoms caused by amantadine intoxication have been published, detailing various types of symptoms and differing times to onset. We encountered a patient who developed CNS symptoms with amantadine. This prompted us to investigate the types, time to onset, and outcome of CNS adverse reactions to amantadine by analyzing data from a pharmacovigilance database.

Patients and methods: The patient was evaluated at Chutoen General Hospital, Shizuoka, Japan. Analysis was performed using the Japanese Adverse Drug Event Report (JADER) database.

Results: In our case, the amantadine blood concentration was 4,042 ng/ml, i.e., in the toxic range. The time to onset was 26 days for dyskinesia and 90 days for depressed level of consciousness. Symptoms resolved when amantadine was discontinued. The JADER database contained 974 cases of adverse reactions to amantadine. The most frequently reported CNS adverse reaction was hallucination, with a reporting odds ratio of 64.28 (95% confidence interval=52.67-78.46). Positive signals were detected for all CNS adverse reactions. For all CNS reactions, clinical outcomes were poor in a comparatively low percentage of cases. Most CNS reactions occurred soon after administration of amantadine, usually within approximately one month.

Conclusion: Because most CNS adverse reactions to amantadine usually occur within approximately one month of initiating treatment, healthcare providers should exercise heightened vigilance in monitoring patients for such reactions during this period.

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金刚烷胺中毒引起的中枢神经系统不良反应:病例报告和 JADER 分析。
背景/目的:关于金刚烷胺中毒导致中枢神经系统(CNS)症状的病例报告已发表过几篇,详细描述了各种类型的症状和不同的发病时间。我们遇到过一名因服用金刚烷胺而出现中枢神经系统症状的患者。这促使我们通过分析药物警戒数据库中的数据,调查金刚烷胺引起的中枢神经系统不良反应的类型、发病时间和结果:患者和方法:患者在日本静冈县中土园综合医院接受了评估。使用日本药物不良事件报告(JADER)数据库进行分析:在我们的病例中,金刚烷胺的血药浓度为 4,042 纳克/毫升,即在中毒范围内。运动障碍的发病时间为 26 天,意识障碍的发病时间为 90 天。停用金刚烷胺后症状消失。JADER 数据库包含 974 例金刚烷胺不良反应病例。最常报告的中枢神经系统不良反应是幻觉,报告几率比为 64.28(95% 置信区间=52.67-78.46)。所有中枢神经系统不良反应均检测到阳性信号。在所有中枢神经系统不良反应中,临床结果不佳的病例比例相对较低。大多数中枢神经系统不良反应发生在服用金刚烷胺后不久,通常在一个月左右:结论:由于金刚烷胺的大多数中枢神经系统不良反应通常发生在开始治疗后约一个月内,因此医护人员应在此期间提高警惕,监测患者是否出现此类不良反应。
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来源期刊
In vivo
In vivo 医学-医学:研究与实验
CiteScore
4.20
自引率
4.30%
发文量
330
审稿时长
3-8 weeks
期刊介绍: IN VIVO is an international peer-reviewed journal designed to bring together original high quality works and reviews on experimental and clinical biomedical research within the frames of physiology, pathology and disease management. The topics of IN VIVO include: 1. Experimental development and application of new diagnostic and therapeutic procedures; 2. Pharmacological and toxicological evaluation of new drugs, drug combinations and drug delivery systems; 3. Clinical trials; 4. Development and characterization of models of biomedical research; 5. Cancer diagnosis and treatment; 6. Immunotherapy and vaccines; 7. Radiotherapy, Imaging; 8. Tissue engineering, Regenerative medicine; 9. Carcinogenesis.
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