Sales Ibrahim, Aljadhey Hisham, Albogami Yasser, Mahmoud Mansour A
College of Pharmacy, Clinical Pharmacy Department, King Saud University, Riyadh, Saudi Arabia.
Medication Safety Research Chair, King Saud University, Riyadh, Saudi Arabia.
Saudi Pharm J. 2017 Sep;25(6):868-872. doi: 10.1016/j.jsps.2017.01.004. Epub 2017 Jan 25.
To assess the general public awareness and perception about Adverse Drug Reactions (ADRs) reporting and pharmacovigilance. A cross-sectional study conducted on June 2012 during awareness campaign held in two malls in Riyadh city for two days. A self-administered questionnaire consisting of three parts was distributed to the attendees who accepted to participate in the study. A total of 204 questionnaires were collected with a response rate of 68%. Twenty-three percent could correctly define ADRs. Only 13(15.7%) of responders were familiar with the term "Pharmacovigilance" and only 78.6% were aware about the Saudi Pharmacovigilance Center. Sixty-seventy percent indicated that their physicians or pharmacists don't actively encourage them to report ADRs that may occur when they take their medications. The majority of responders (73.2%) believed that the medical team, rather than consumers, should report ADRs. When asked why patients do not report ADRs, 19.1(48.5%) believed that patients do not know whether the ADR is from the medication or not, 18.1(46.1%) stated that the reason was because patients don't know about the Pharmacovigilance Center, 16(40.7%) think that patients don't know about the importance of ADRs reporting, and 14(36.3%) responded that patients probably don't know how to report ADRs. The general public in Saudi Arabia are not aware about ADRs reporting and the pharmacovigilance system. The Saudi Food and Drug Authorities (FDA) need to put more efforts to increasing public awareness about the importance of ADRs reporting process and the importance of pharmacovigilance system in promoting patient safety.
评估公众对药品不良反应(ADR)报告及药物警戒的认知和看法。2012年6月在利雅得市的两个商场举行为期两天的宣传活动期间开展了一项横断面研究。一份由三部分组成的自填式问卷被分发给同意参与研究的参与者。共收集到204份问卷,回复率为68%。23%的人能够正确定义药品不良反应。只有13名(15.7%)应答者熟悉“药物警戒”一词,只有78.6%的人知道沙特药物警戒中心。67%的人表示他们的医生或药剂师没有积极鼓励他们报告服药时可能出现的药品不良反应。大多数应答者(73.2%)认为应由医疗团队而非消费者报告药品不良反应。当被问及患者为何不报告药品不良反应时,19.1人(48.5%)认为患者不知道药品不良反应是否由药物引起,18.1人(46.1%)表示原因是患者不了解药物警戒中心,16人(40.7%)认为患者不了解药品不良反应报告的重要性,14人(36.3%)回答患者可能不知道如何报告药品不良反应。沙特阿拉伯的公众对药品不良反应报告和药物警戒系统并不了解。沙特食品药品管理局(FDA)需要加大力度提高公众对药品不良反应报告过程的重要性以及药物警戒系统在促进患者安全方面的重要性的认识。