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伊朗药品说明书评估

Evaluation of Medication Package Inserts in Iran.

作者信息

Khamas Shahriyar Shahbazi, Jafari Atefeh, Zarif-Yeganeh Morvarid, Taghvaye-Masoumi Hamidreza

机构信息

Students' Research Committee, School of Pharmacy, Guilan University of Medical Sciences, Rasht, Gilan, Iran.

Department of Clinical Pharmacy, School of Pharmacy, Guilan University of Medical Sciences, Rasht, Gilan, Iran.

出版信息

J Res Pharm Pract. 2019 Apr-Jun;8(2):45-51. doi: 10.4103/jrpp.JRPP_18_32.

Abstract

OBJECTIVE

Package inserts (PIs) provide information for the safe and effective use of medication. There is no study on the evaluation of PIs in Iran. The purpose of this study was to evaluate the completeness of PIs supplied with the 100 top-selling medications in Iran.

METHODS

This cross-sectional observational study was conducted during 3 weeks in January 2017. One hundred medications were chosen from a list supplied by the Iran Food and Drug Administration (IFDA). The PIs were assessed for the presentation and completeness of quality criteria, which was consisted of two parts. The first part was the criteria required by the IFDA, mentioned in Chapter 16 of the Pharmaceutical Regulations and Instructions provided by the IFDA. The second part of the criteria was defined according to the critical comments of clinical and industrial pharmacists.

FINDINGS

Thirty-seven out of 100 medications included no PIs. None of the PIs met all the criteria required by the IFDA. The highest score for completeness was 18 out of 21 (85.7%). Medication name, description, and adverse reaction were mentioned in all PIs. Other items such as patient counseling information (98%), warnings (95.2%), precautions (95.2%), pregnancy/lactation (95%), and storage condition (90.5%) have been mentioned in a high percentage of PIs.

CONCLUSION

PIs have improved in recent years in Iran, but there is an absolute need for more accurate and up-to-date information. The IFDA should supervise pharmaceutical companies more strictly in this regard and should revise its regulations requiring PIs to conform to the FDA regulations.

摘要

目的

药品说明书为药物的安全有效使用提供信息。伊朗尚无关于药品说明书评估的研究。本研究旨在评估伊朗最畅销的100种药品所附药品说明书的完整性。

方法

本横断面观察性研究于2017年1月进行了3周。从伊朗食品药品管理局(IFDA)提供的清单中选取了100种药品。对药品说明书的呈现和质量标准的完整性进行评估,质量标准由两部分组成。第一部分是IFDA要求的标准,在IFDA提供的《药品法规与说明》第16章中有提及。标准的第二部分是根据临床和工业药剂师的关键意见确定的。

结果

100种药品中有37种没有药品说明书。没有一份药品说明书符合IFDA要求的所有标准。完整性的最高分是21分中的18分(85.7%)。所有药品说明书都提到了药品名称、描述和不良反应。其他项目,如患者咨询信息(98%)、警告(95.2%)、注意事项(95.2%)、妊娠/哺乳期(95%)和储存条件(90.5%)在大多数药品说明书中都有提及。

结论

近年来伊朗的药品说明书有了改进,但绝对需要更准确和最新的信息。IFDA在这方面应更严格地监督制药公司,并应修订其要求药品说明书符合FDA法规的规定。

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