Journal of Pharmacy And Bioallied Sciences

ORIGINAL ARTICLE
Year
: 2021  |  Volume : 13  |  Issue : 3  |  Page : 325--330

Retrospective assessment of the reporting of adverse drug reactions in a Malaysian clinical training center: A short communication


Ramadan M Elkalmi1, Mohamed Hassan Elnaem2, Nurmisaliza Mohd Sapar3, Ali Blebil4 
1 Department of Pharmacology, Faculty of Medicine, Sebha University, Sabha, Libya
2 Department of Pharmacy Practice, Kulliyyah of Pharmacy; Quality Use of Medicines Research Group, Kulliyyah of Pharmacy, International Islamic University Malaysia, Kuantan, Pahang, Malaysia
3 Department of Pharmacy Practice, Faculty of Pharmacy, Universiti Teknologi Mara, Selangor, Malaysia
4 Department of Pharmacy Practice, School of Pharmacy, Monash University Malaysia, Bandar Sunway, Selangor, Malaysia

Correspondence Address:
Dr. Ramadan M Elkalmi
Department of Pharmacology, Faculty of Medicine, Sebha University, Sebha, Libya; Department of Clinical Pharmacy and Pharmacotherapeutics, Dubai Pharmacy College for Girls, Dubai, United Arab Emirates

Objectives: This study aimed to assess the completeness and quality of adverse drug reaction (ADR) reports that were submitted to the Pharmacovigilance Unit (PVU) in clinical training center (CTC), Faculty of Medicine, UiTM Sungai Buloh Campus. Materials and Methods: A retrospective study was conducted using all ADR reports that were submitted to the PVU in CTC from December 31, 2000, to December 31, 2018. The completeness was assessed by reviewing all the required elements to be filled in the ADR reports. The quality was assessed by investigating the required information in the ADR reporting form. Descriptive statistics have been used to present the findings. Key Findings: In a total of 31 reports that were submitted to the PVU in CTC, 98.9% of patient's information and 100% of ADR descriptions were completed. Suspected drug information and the reporter's details were completed by 52.2% and 79.6%, respectively. Of 58.0% of the information about seriousness recorded, 38.9% (n = 7) is mild, 44.4% (n = 8) is moderate, and 16.7% (n = 3) is severe. Among all the suspected medicines, drug class of antibiotics (32.4%, n = 12) is the most reported suspected drugs that caused ADR, followed by opioid analgesic (8.1%, n = 3) and nonsteroidal anti-inflammatory drugs (8.1%, n = 3). Conclusion: Further efforts and relevant interventions should be considered to increase the reporting frequency and to enhance the completeness and the quality of the ADR reports in the study setting.


How to cite this article:
Elkalmi RM, Elnaem MH, Sapar NM, Blebil A. Retrospective assessment of the reporting of adverse drug reactions in a Malaysian clinical training center: A short communication.J Pharm Bioall Sci 2021;13:325-330


How to cite this URL:
Elkalmi RM, Elnaem MH, Sapar NM, Blebil A. Retrospective assessment of the reporting of adverse drug reactions in a Malaysian clinical training center: A short communication. J Pharm Bioall Sci [serial online] 2021 [cited 2022 Jan 25 ];13:325-330
Available from: https://www.jpbsonline.org/article.asp?issn=0975-7406;year=2021;volume=13;issue=3;spage=325;epage=330;aulast=Elkalmi;type=0