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口服布南色林治疗精神分裂症的安全性和有效性:日本上市后监测研究综述。

Safety and effectiveness of oral blonanserin for schizophrenia: A review of Japanese post-marketing surveillances.

机构信息

Medical Affairs, Sumitomo Dainippon Pharma Co., Ltd., Tokyo, Japan.

Corporate Governance Material Review Group, Sumitomo Dainippon Pharma Co., Ltd., Osaka, Japan.

出版信息

J Pharmacol Sci. 2021 Jan;145(1):42-51. doi: 10.1016/j.jphs.2020.09.006. Epub 2020 Oct 8.

DOI:10.1016/j.jphs.2020.09.006
PMID:33357778
Abstract

Schizophrenia significantly limits social functioning with positive and negative symptoms and cognitive dysfunction. Blonanserin (LONASEN®), a novel second-generation antipsychotic approved for treating schizophrenia in Japan in 2008, reportedly shows beneficial effects on cognitive function as well as positive and negative symptoms, with potential for improving social functioning. To understand the safety and effectiveness of blonanserin in the real clinical practice, five Japanese post-marketing surveillances have been conducted and published to date. In this article, we reviewed all the Japanese post-marketing surveillances and discussed the clinical usefulness of blonanserin in patients with schizophrenia having diverse clinical characteristics. Adverse drug reactions, such as akathisia and extrapyramidal symptoms, were common in all surveillances. However, those specific to second-generation antipsychotics, such as weight gain and abnormalities in glycometabolism or lipid metabolism, were rarely observed. In addition, no adverse drug reactions apart from clinical trial results were found. Brief Psychiatric Rating Scale total scores in all surveillances significantly lowered at the last evaluation than at baseline. These results were consistent through 1-year of treatment, suggesting that effectiveness is maintained even after long-term use. In conclusion, blonanserin is considered a beneficial drug in real clinical practice for patients with schizophrenia having diverse characteristics.

摘要

精神分裂症的阳性和阴性症状以及认知功能障碍显著限制了社会功能。布南色林(LONASEN®)是一种新型的第二代抗精神病药物,于 2008 年在日本获批用于治疗精神分裂症,据报道,它对认知功能以及阳性和阴性症状均有有益的影响,并有改善社会功能的潜力。为了了解布南色林在真实临床实践中的安全性和有效性,迄今为止已经进行了五项日本上市后监测并已发表。在本文中,我们回顾了所有的日本上市后监测,并讨论了布南色林在具有不同临床特征的精神分裂症患者中的临床应用价值。在所有监测中,常见的不良反应有静坐不能和锥体外系症状。然而,像体重增加以及糖代谢或脂代谢异常等第二代抗精神病药物特有的不良反应很少观察到。此外,除临床试验结果外,未发现其他不良反应。所有监测的简明精神病评定量表总分在最后一次评估时均显著低于基线。这些结果在 1 年的治疗期间保持一致,表明即使长期使用,疗效也能维持。总之,布南色林被认为是一种对具有不同特征的精神分裂症患者具有临床价值的药物。

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