Bogowicz Paul, Mehta Aashna, Choudhary Shruti, Brhlikova Petra, Roderick Peter, McGettigan Patricia, Farooqui Habib Hasan, Sharma Aditya Narain, Pollock Allyson M
Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
Indian Institute of Public Health - Delhi, Public Health Foundation of India, Gurugram, India.
J Pharm Policy Pract. 2024 Aug 6;17(1):2372089. doi: 10.1080/20523211.2024.2372089. eCollection 2024.
There is limited evidence to support use of fixed dose combination (FDC) drugs in the treatment of psychiatric disorders. This study aimed to examine the sales and regulatory status of psychotropic FDCs in India, in the context of two government regulatory initiatives.
Official documents were searched to establish an account of the initiatives and measures targeting psychotropic FDCs. This was integrated with private market data (2008 to 2020). Descriptive statistics were used to examine changes in FDC numbers/formulations and sales volumes in standard units (SU) over time.
Psychotropic FDC sales volumes (percentage market share) increased from 0.8 billion SU (18.4%) in 2008 to 1.4 billion SU (20.1%) in 2020. The numbers (formulations) of FDCs also increased, from 28 (101) in 2008 to 33 (143) in 2020. Unapproved FDCs accounted for 69.3% of psychotropic FDC sales in 2008, decreasing slightly to 60.3% in 2020. Of 21 psychotropic FDCs considered under the regulatory initiatives, three went on to be banned, and two of these remained on the market in 2020.
Unapproved FDCs continue to account for most psychotropic FDC sales, potentially putting the public at risk because their safety and efficacy have not been evaluated.
支持使用固定剂量复方制剂(FDC)治疗精神疾病的证据有限。本研究旨在结合两项政府监管举措,考察印度精神类FDC的销售及监管状况。
检索官方文件以梳理针对精神类FDC的举措和措施,并与私人市场数据(2008年至2020年)相结合。运用描述性统计方法考察FDC数量/剂型以及标准单位(SU)销售量随时间的变化。
精神类FDC的销售量(市场份额百分比)从2008年的8亿SU(18.4%)增至2020年的14亿SU(20.1%)。FDC的数量(剂型)也有所增加,从2008年的28种(101个剂型)增至2020年的33种(143个剂型)。2008年,未获批的FDC占精神类FDC销售额的69.3%,到2020年这一比例略有下降,为60.3%。在监管举措所涉及的21种精神类FDC中,有3种被禁,其中2种在2020年仍在市场上销售。
未获批的FDC仍占精神类FDC销售额的大部分,因其安全性和有效性未经评估,可能会使公众面临风险。