Literature DB >> 22316142

Suboptimal reporting of adverse medical events to the FDA Adverse Events Reporting System by nurse practitioners and physician assistants.

Eli D Ehrenpreis1, Humberto Sifuentes, Jamie E Ehrenpreis, Zachary L Smith, Mike L Marshall.   

Abstract

OBJECTIVES: The Adverse Events Reporting System (AERS) of the FDA is used to identify toxicities of drugs that are on the market. Nurse practitioners (NP) and physician assistants (PA), having an increasing role in the delivery of medical care, are also needed to participate in post-marketing pharmacovigilance. This study was performed to assess awareness and use of the AERS in voluntary reporting of drug toxicities by NPs and PAs.
METHODS: A cluster sample survey was issued at the Principles of Gastroenterology for the Nurse Practitioner and Physician Assistant course in August 2010. The survey assessed familiarity with the AERS, the number of adverse events seen and the frequency of reports sent to the AERS. NP and PA responses were compared using the two-tailed Fisher's exact.
RESULTS: Of the 92 respondents, 67 (72%) were NPs and 24 (26%) PAs. Of the 50 (54%) respondents that reported being familiar with the AERS system, 20 (40%) incorrectly identified the methods to report using the AERS. Overall reporting of adverse events was low, particularly in respondents seeing 5-12 adverse events per year.
CONCLUSION: The study suggests that improved education regarding the importance of using AERS for pharmacovigilance is suggested for NPs and PAs. Due to the small size of the study, these data should be viewed as preliminary, pending a larger confirmatory study.

Entities:  

Mesh:

Year:  2012        PMID: 22316142     DOI: 10.1517/14740338.2012.650165

Source DB:  PubMed          Journal:  Expert Opin Drug Saf        ISSN: 1474-0338            Impact factor:   4.250


  4 in total

Review 1.  The key role of clinical and community health nurses in pharmacovigilance.

Authors:  Caterina Bigi; Guido Bocci
Journal:  Eur J Clin Pharmacol       Date:  2017-08-02       Impact factor: 2.953

2.  Using structured telephone follow-up assessments to improve suicide-related adverse event detection.

Authors:  Sarah A Arias; Zi Zhang; Carla Hillerns; Ashley F Sullivan; Edwin D Boudreaux; Ivan Miller; Carlos A Camargo
Journal:  Suicide Life Threat Behav       Date:  2014-03-03

Review 3.  Data mining of the public version of the FDA Adverse Event Reporting System.

Authors:  Toshiyuki Sakaeda; Akiko Tamon; Kaori Kadoyama; Yasushi Okuno
Journal:  Int J Med Sci       Date:  2013-04-25       Impact factor: 3.738

Review 4.  Development of a theoretical framework of factors affecting patient safety incident reporting: a theoretical review of the literature.

Authors:  Stephanie Archer; Louise Hull; Tayana Soukup; Erik Mayer; Thanos Athanasiou; Nick Sevdalis; Ara Darzi
Journal:  BMJ Open       Date:  2017-12-27       Impact factor: 2.692

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.