首页> 外文期刊>Pharmacoepidemiology and drug safety >Switching patterns of immediate-release forms of generic mixed amphetamine salts products among privately and publicly insured individuals aged 15-64 years in the United States, 2013-2019
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Switching patterns of immediate-release forms of generic mixed amphetamine salts products among privately and publicly insured individuals aged 15-64 years in the United States, 2013-2019

机译:2013-2019 年美国 15-64 岁私人和公共保险个人中通用混合苯丙胺盐产品的速释型转换模式

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PurposeImmediate-release forms of generic mixed amphetamine salts (MAS) have been the subject of passive surveillance reports signaling lack of effectiveness. We examined switching patterns that might suggest whether long-term users of specific MAS are more likely to switch away or switch back after use of the MAS of interest in the FDA's Sentinel Distributed Database. MethodsWe required at least 60-day continuous supply of selected MAS grouped by Abbreviated New Drug Application (ANDA) to describe patterns of switching away from and to generics approved under the ANDAs of interest among individuals ages 15-64 years with attention deficit hyperactivity disorder or narcolepsy during 2013-2019. ResultsWe observed the greatest number of treatment episodes for ANDA 040422 (n = 525 771), followed by ANDA 202424 (n = 181 693), ANDA 040439 (n = 62 363), ANDA 040440 (n = 21 143), and ANDA 040480 (n = 8792). Of those with switches away from their original ANDA, episodes initiated on generic products under ANDA 040422 (48.6) and ANDA 202424 (43.0) were most likely to switch back, while those initiated on generic product under ANDA 040480 were least likely (24.1). Of those episodes with switches to a generic under an ANDA of interest, about one-third (range 27.1 to 37.0) switched back to the same product. These switches back had a median time to switch of about 30 days. ConclusionsThese descriptive analyses, although subject to limitations, did not suggest increased switching away or switching back after use of the generics of interest. Continued post-marketing surveillance is warranted.
机译:目的通用混合苯丙胺盐 (MAS) 的速释形式一直是被动监测报告的主题,表明缺乏有效性。我们研究了切换模式,这些模式可能表明特定 MAS 的长期用户在使用 FDA 的 Sentinel 分布式数据库中感兴趣的 MAS 后是否更有可能切换或切换回来。方法我们要求至少连续供应 60 天按简化新药申请 (ANDA) 分组的选定 MAS,以描述在 2013-2019 年期间 15-64 岁患有注意力缺陷多动障碍或发作性睡病的个体中,从和转换到 ANDA 批准的仿制药的模式。结果ANDA 040422治疗发作次数最多(n = 525 771),其次是ANDA 202424(n = 181 693)、ANDA 040439(n = 62 363)、ANDA 040440(n = 21 143)和ANDA 040480(n = 8792)。在那些从原来的ANDA转换的患者中,根据ANDA 040422(48.6%)和ANDA 202424(43.0%)在仿制药上启动的发作最有可能切换回来,而在ANDA 040480下的仿制药产品上启动的发作最不可能(24.1%)。在根据感兴趣的ANDA切换到仿制药的剧集中,约三分之一(范围为27.1%至37.0%)改回同一产品。这些切换回来的中位切换时间约为 30 天。结论这些描述性分析虽然存在局限性,但并未表明在使用感兴趣的仿制药后,切换或切换回来的情况有所增加。有必要继续进行上市后监测。

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