Safety risks with investigational drugs: Pharmacy practices and perceptions in the veterans affairs health system
- PMID: 26240744
- PMCID: PMC4519741
- DOI: 10.1177/2042098615584924
Safety risks with investigational drugs: Pharmacy practices and perceptions in the veterans affairs health system
Abstract
Objectives: Rigorous practices for safe dispensing of investigational drugs are not standardized. This investigation sought to identify error-prevention processes utilized in the provision of investigational drug services (IDS) and to characterize pharmacists' perceptions about safety risks posed by investigational drugs.
Methods: An electronic questionnaire was distributed to an audience of IDS pharmacists within the Veteran Affairs Health System. Multiple facets were examined including demographics, perceptions of medication safety, and standard processes used to support investigational drug protocols.
Results: Twenty-one respondents (32.8% response rate) from the Northeast, Midwest, South, West, and Non-contiguous United States participated. The mean number of pharmacist full-time equivalents (FTEs) dedicated to the IDS was 0.77 per site with 0.2 technician FTEs. The mean number of active protocols was 22. Seventeen respondents (81%) indicated some level of concern for safety risks. Concerns related to the packaging of medications were expressed, most notably lack of product differentiation, expiration dating, barcodes, and choice of font size or color. Regarding medication safety practices, the majority of sites had specific procedures in place for storing and securing drug supply, temperature monitoring, and prescription labeling. Repackaging bulk items and proactive error-identification strategies were less common. Sixty-seven percent of respondents reported that an independent double check was not routinely performed.
Conclusions: Medication safety concerns exist among pharmacists in an investigational drug service; however, a variety of measures have been employed to improve medication safety practices. Best practices for the safe dispensing of investigational medications should be developed in order to standardize these error-prevention strategies.
Keywords: clinical trials; investigational drugs; medication safety; pharmacy practice; research pharmacist.
Conflict of interest statement
Figures
Similar articles
-
Medication Safety in Clinical Trials: Role of the Pharmacist in Optimizing Practice, Collaboration, and Education to Reduce Errors.Yale J Biol Med. 2017 Mar 29;90(1):125-133. eCollection 2017 Mar. Yale J Biol Med. 2017. PMID: 28356900 Free PMC article. Review.
-
Utilization of Technology to Improve Efficiency in Investigational Drug Management Processes.J Pharm Technol. 2020 Apr;36(2):84-90. doi: 10.1177/8755122519900049. Epub 2020 Jan 22. J Pharm Technol. 2020. PMID: 34752537 Free PMC article.
-
Improving investigational drug service operations through development of an innovative computer system.Am J Health Syst Pharm. 2008 May 15;65(10):969-73. doi: 10.2146/ajhp070212. Am J Health Syst Pharm. 2008. PMID: 18463347
-
The impacts of a pharmacist-managed outpatient clinic and chemotherapy-directed electronic order sets for monitoring oral chemotherapy.J Oncol Pharm Pract. 2017 Dec;23(8):582-590. doi: 10.1177/1078155216672314. Epub 2016 Oct 12. J Oncol Pharm Pract. 2017. PMID: 27733666
-
Development and funding of a pharmacy-based investigational drug service.Am J Hosp Pharm. 1987 May;44(5):1069-74. Am J Hosp Pharm. 1987. PMID: 3605116
Cited by
-
Medication Safety in Clinical Trials: Role of the Pharmacist in Optimizing Practice, Collaboration, and Education to Reduce Errors.Yale J Biol Med. 2017 Mar 29;90(1):125-133. eCollection 2017 Mar. Yale J Biol Med. 2017. PMID: 28356900 Free PMC article. Review.
-
Economic outcomes associated with an investigational drug service within a Veterans Affairs health care system.Contemp Clin Trials Commun. 2019 Apr 6;14:100354. doi: 10.1016/j.conctc.2019.100354. eCollection 2019 Jun. Contemp Clin Trials Commun. 2019. PMID: 31011657 Free PMC article.
-
Audit experiences in investigational medicinal product management and errors in clinical trials.Trials. 2025 Mar 21;26(1):100. doi: 10.1186/s13063-025-08795-w. Trials. 2025. PMID: 40119366 Free PMC article.
References
-
- Cohen I., Foote M., Kirking D., Tankanow R., Conlon P. (1989) Investigational drug practices in Michigan hospitals. Am J Hosp Pharm 46: 1370-1375. - PubMed
-
- FDA (US Food and Drug Administration) (2013) Investigational new drug application, C.F.R. 21, Section 312. Available at: http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?CF... (accessed June 2014).
-
- HOPA (Hematology/Oncology Pharmacy Association) (2014) HOPA investigational drug service best practice standards. Available at: http://www.hoparx.org/uploads/files/2014/HOPA14_IDS_Guidelines_Final.pdf (accessed March 2015).
-
- ISMP (Institute for Safe Medication Practices) (1997) ISMP medication safety alert! Safety problems posed by investigational drug name abbreviations and acronyms. Available at: http://www.ismp.org/newsletters/acutecare/articles/19971203.asp (accessed May 2014).
LinkOut - more resources
Full Text Sources
Other Literature Sources