Pastuszak Alexander W, Hu Yiqun, Freid Jeffrey D
Division of Urology, Department of Surgery, University of Utah School of Medicine, Salt Lake City, UT, USA.
Medical Affairs, Endo Pharmaceuticals Inc, Malvern, PA, USA.
Sex Med. 2020 Jun;8(2):237-242. doi: 10.1016/j.esxm.2020.01.009. Epub 2020 Mar 14.
The Aveed Risk Evaluation and Mitigation Strategy program was instituted because of potential risk of pulmonary oil microembolism (POME) and/or anaphylaxis after intramuscular injection of Aveed (testosterone undecanoate), indicated for treatment of adult male patients with congenital or acquired primary hypogonadism or hypogonadotropic hypogonadism.
To analyze the reporting rate of POME associated with testosterone undecanoate administration (750 mg/3 mL) during postmarketing surveillance.
The Endo Pharmaceuticals Inc database was searched for POME reports occurring from testosterone undecanoate approval on March 5, 2014, through June 30, 2018. Each case was reviewed and adjudicated by a drug safety physician to confirm the reported event had predefined clinical characteristics consistent with POME.
Annual rate and clinical features of spontaneously reported POME cases were characterized.
During the 4.3-year period, 90,092 doses of intramuscular testosterone undecanoate were distributed via an Aveed Risk Evaluation and Mitigation Strategy program to health-care professionals for patient treatment. Of 633 individual case safety reports in the Endo Pharmaceuticals Inc safety database, 28 spontaneously reported adverse events were classified as POME, for a yearly spontaneously reported adverse event per-injection rate of <0.1%. Most (21/22) events resolved, and of those with a resolution time reported, most (13/17) resolved in ≤30 minutes. More than 60% (13/21) of patients required no medical intervention (ie, the POME event resolved spontaneously). One fatality was reported 18 months after a documented POME event and appeared unrelated to the reported testosterone undecanoate injection or subsequent injections after the POME event. In 3 out of 4 POME cases with symptoms serious enough to require an emergency room visit, issues with injection technique or dosing were identified as a potential contributing factor.
Injection technique and proper product usage are key elements in the prevention of POME events.
STRENGTHS & LIMITATIONS: The reported rate of POME events was determined from a real-world clinical practice patient population; however, postmarketing safety data typically are underreported and retrospective in nature.
POME events appear to be rare, with resolution occurring quickly without medical intervention in most cases. Pastuszak AW, Hu Y, Freid JD. Occurrence of Pulmonary Oil Microembolism After Testosterone Undecanoate Injection: A Postmarketing Safety Analysis. Sex Med 2020;8:237-242.
由于肌肉注射Aveed(十一酸睾酮)后存在肺油微栓塞(POME)和/或过敏反应的潜在风险,因此设立了Aveed风险评估和缓解策略计划。Aveed用于治疗患有先天性或后天性原发性性腺功能减退或促性腺激素缺乏性性腺功能减退的成年男性患者。
分析上市后监测期间与十一酸睾酮给药(750mg/3mL)相关的POME报告率。
在Endo制药公司数据库中搜索2014年3月5日十一酸睾酮获批至2018年6月30日期间发生的POME报告。每例病例均由一名药物安全医师进行审查和判定,以确认报告的事件具有与POME一致的预定义临床特征。
对自发报告的POME病例的年发生率和临床特征进行了描述。
在4.3年期间,通过Aveed风险评估和缓解策略计划向医疗保健专业人员分发了90,092剂肌肉注射用十一酸睾酮用于患者治疗。在Endo制药公司安全数据库中的633份个体病例安全报告中,28例自发报告的不良事件被归类为POME,年自发报告的每注射不良事件发生率<0.1%。大多数(21/22)事件得到解决,在报告了缓解时间的事件中,大多数(13/17)在≤30分钟内得到解决。超过60%(13/21)的患者无需医疗干预(即POME事件自发解决)。在一次记录在案的POME事件发生18个月后报告了1例死亡病例,该死亡病例似乎与报告的十一酸睾酮注射或POME事件后的后续注射无关。在4例症状严重到需要去急诊室就诊的POME病例中,有3例发现注射技术或剂量问题是一个潜在的促成因素。
注射技术和正确使用产品是预防POME事件的关键因素。
POME事件的报告率是根据真实世界临床实践患者群体确定的;然而,上市后安全数据通常报告不足且本质上是回顾性的。
POME事件似乎很少见,大多数情况下无需医疗干预即可迅速解决。Pastuszak AW, Hu Y, Freid JD. 十一酸睾酮注射后肺油微栓塞的发生情况:一项上市后安全性分析。性医学2020;8:237 - 242。