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美国食品药品监督管理局(FDA)关于西地那非和注射用前列地尔相关患者死亡报告的比较。

Comparison of FDA reports of patient deaths associated with sildenafil and with injectable alprostadil.

作者信息

Cohen J S

机构信息

Department of Family and Preventive Medicine, University of California, San Diego, La Jolla, USA.

出版信息

Ann Pharmacother. 2001 Mar;35(3):285-8. doi: 10.1345/aph.10218.

Abstract

BACKGROUND

Sildenafil (Viagra) has been linked to 240 deaths (128 verified, 112 unverified) reported to the Food and Drug Administration (FDA) during 7.5 months of availability, and to 522 reported deaths after 13 months of availability. To date, no updated information about FDA-reported deaths has emerged, and no comparative analyses have been published.

OBJECTIVE

To compare the mortality rates between sildenafil and injectable alprostadil, both of which are used exclusively for treating erectile dysfunction.

METHODS

A comparison of the number of deaths per filled prescriptions reported to the FDA involving sildenafil and injectable alprostadil was undertaken to perhaps provide further insight into this issue. Materials included FDA statements on sildenafil adverse event reports to the FDA involving sildenafil and injectable alprostadil, and data on prescriptions filled for sildenafil and injectable alprostadil.

RESULTS

The number of deaths per prescriptions filled reported in association with sildenafil was significantly greater (5.15-6.28 times) than in association with injectable alprostadil.

DISCUSSION

Previous explanations for sildenafil-associated deaths have been based on the expected attrition within the population of men with erectile dysfunction and its commonly associated disorders, the physiologic stress of renewed sexual activity, and a pharmacologic effect of sildenafil. The results of this analysis may indicate that a pharmacologic effect of sidenafil is responsible for these deaths. However, other factors may also explain these findings: a greater frequency of reporting of sildenafil-associated events by physicians, a difference in the populations using these two drugs, or the number of prescriptions filled may not accurately reflect actual exposure.

CONCLUSIONS

Further study should be undertaken to clarify the issues associated with sildenafil-related deaths. In the meantime, reasonable precautions might be considered in prescribing sildenafil, such as initiating treatment with a low test dose of sildenafil.

摘要

背景

在西地那非(伟哥)上市的7.5个月期间,有240例死亡报告(128例经证实,112例未经证实)被上报至美国食品药品监督管理局(FDA),上市13个月后有522例死亡报告。迄今为止,尚无关于FDA上报死亡病例的最新信息,也没有发表过比较分析。

目的

比较西地那非和注射用前列地尔的死亡率,这两种药物均专门用于治疗勃起功能障碍。

方法

对上报至FDA的涉及西地那非和注射用前列地尔的每份已配处方的死亡人数进行比较,以期对该问题有更深入的了解。材料包括FDA关于西地那非不良事件报告的声明、涉及西地那非和注射用前列地尔的报告,以及西地那非和注射用前列地尔的已配处方数据。

结果

与西地那非相关的每份已配处方的死亡人数显著高于(5.15 - 6.28倍)注射用前列地尔。

讨论

先前对西地那非相关死亡的解释基于勃起功能障碍男性人群及其常见相关疾病的预期损耗、恢复性活动的生理压力以及西地那非的药理作用。该分析结果可能表明西地那非的药理作用是这些死亡的原因。然而,其他因素也可能解释这些发现:医生对西地那非相关事件的报告频率更高、使用这两种药物的人群存在差异,或者已配处方数量可能无法准确反映实际暴露情况。

结论

应进行进一步研究以阐明与西地那非相关死亡有关的问题。同时,在开具西地那非处方时可考虑采取合理的预防措施,如以低测试剂量开始西地那非治疗。

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