J Am Pharm Assoc (2003). 2021 Jan-Feb;61(1):e110-e114. doi: 10.1016/j.japh.2020.08.027. Epub 2020 Sep 14.
The Drug Quality and Security Act passed in 2013 created a new voluntary category of compounders, referred to as outsourcing facilities. The regulatory landscape allows these facilities to compound on a larger scale in comparison with the typical compounding pharmacies, which positions them to potentially serve a role in overcoming drug shortages.
The purpose of this article is to identify the number of drug products on shortage as reported by the Food and Drug Administration (FDA) that were also compounded by outsourcing facilities.
All current and resolved drug shortages through January 27, 2020, as reported by FDA, were compared with the 503B product reports from July 2018 through June 2019 submitted to FDA by outsourcing facilities. The active pharmaceutical ingredient (API) and dosage form for each product on shortage were compared with the 503B product reports to identify similarities.
There were 344 unique APIs on the FDA drug shortage list and 774 unique APIs on the 503B product reports. After comparison of the APIs on the drug shortage list with those on the product reports, 27% of unique APIs (74 of 272) were included on both lists, and of these, 18% (50 of 272) of the APIs on the drug shortage list were compounded by outsourcing facilities in the same dosage form as what was on shortage.
The regulatory landscape positions outsourcing facilities to play an important role in providing access to medications while on shortage. However, when comparing the drugs on shortage as reported by FDA with the 503B product reports, there was minimal overlap. Additional research into why outsourcing facilities are not taking on a larger role in overcoming drug shortages should be explored.
2013 年通过的《药品质量和安全法案》创建了一个新的化合物师自愿类别,称为外包设施。与典型的化合物药房相比,监管环境允许这些设施进行更大规模的化合物生产,这使它们有潜力在克服药品短缺方面发挥作用。
本文旨在确定食品和药物管理局(FDA)报告的短缺药品中有多少是由外包设施复合的。
将所有截至 2020 年 1 月 27 日的当前和已解决的药品短缺情况与 2018 年 7 月至 2019 年 6 月期间外包设施向 FDA 提交的 503B 产品报告进行比较。将短缺药品中的活性药物成分(API)和剂型与 503B 产品报告进行比较,以确定相似之处。
FDA 药品短缺清单上有 344 种独特的 API,503B 产品报告上有 774 种独特的 API。在将药品短缺清单上的 API 与产品报告上的 API 进行比较后,27%的独特 API(272 个中的 74 个)同时出现在两个清单上,其中 18%(272 个中的 50 个)药品短缺清单上的 API 以短缺的剂型由外包设施复合。
监管环境使外包设施在药品短缺时能够发挥重要作用提供药物。然而,当将 FDA 报告的短缺药品与 503B 产品报告进行比较时,两者之间几乎没有重叠。应该进一步研究为什么外包设施在克服药品短缺方面没有发挥更大的作用。