Saudi Food and Drug Authority, Riyadh, Saudi Arabia.
College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Pharmacol Res Perspect. 2021 May;9(3):e00763. doi: 10.1002/prp2.763.
A retrospective observational study evaluated the direct healthcare professional communication (DHPC) letters disseminated by the Saudi Food and Drug Authority (SFDA) and their compliance with the pharmacovigilance guidelines. The study was utilized all DHPC letters available on the SFDA website, which is intended to communicate drug safety information to healthcare professionals (HCPs). Then, the letters were evaluated based on DHPC letter requirements approved in the European Medicines Agency (EMA) pharmacovigilance guidelines. Statistical analyses were conducted utilizing statistical analysis software (SAS version 9.4). In June 2020, 169 letters were retrieved from the SFDA website. Most of the letters had the marketing authorization holder's logo (97%) and mentioned the date of letter issuance (98.8%). The most frequently discussed safety issues were hyperkalemia risk associated with combining renin-angiotensin-aldosterone system (RAAS) medications (10.6%) and cardiac risks (9%). Antineoplastic and immunosuppressant classes were associated with a majority of DHPC letters (15% for each category). A significant percentage of DHPC letters (10%) did not mention an agreement statement with SFDA, and 42 letters did not include marketing authorization holders (MAHs) contact information. The qualified persons responsible for pharmacovigilance and medical directors had signed most of the DHPC letters (51% and 46%, respectively). Many letters mentioned the details of reporting information to both SFDA and an MAH (82%). Moreover, 66% of the DHPC letters presented safety information within the 2-page limit. In conclusion, the DHPC letters disseminated by MAHs in Saudi Arabia have an acceptable level of compliance with the guidelines.
一项回顾性观察研究评估了沙特食品药品管理局(SFDA)发布的直接医疗专业人员沟通(DHPC)信件及其对药物警戒指南的遵守情况。该研究使用了 SFDA 网站上提供的所有 DHPC 信件,旨在向医疗保健专业人员(HCPs)传达药物安全信息。然后,根据欧洲药品管理局(EMA)药物警戒指南中批准的 DHPC 信件要求对这些信件进行评估。统计分析使用统计分析软件(SAS 版本 9.4)进行。2020 年 6 月,从 SFDA 网站检索到 169 封信件。大多数信件都有营销授权持有人的标志(97%)并提到了信件签发日期(98.8%)。讨论最多的安全问题是与联合使用肾素-血管紧张素-醛固酮系统(RAAS)药物相关的高钾血症风险(10.6%)和心脏风险(9%)。抗肿瘤和免疫抑制剂类药物与大多数 DHPC 信件相关(每类占 15%)。相当一部分 DHPC 信件(10%)未提及与 SFDA 的协议声明,42 封信未包含营销授权持有人(MAHs)的联系信息。负责药物警戒和医学主任的合格人员签署了大多数 DHPC 信件(分别为 51%和 46%)。许多信件都提到了向 SFDA 和 MAH 报告信息的详细信息(82%)。此外,66%的 DHPC 信件在 2 页限制内提供了安全信息。总之,沙特阿拉伯 MAHs 发布的 DHPC 信件在很大程度上符合指南的要求。