Examination of pharmacists’ intention to report serious adverse drug events (ADEs) to the FDA using the theory of planned behavior |
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Authors: | Paul Gavaza Ph.D. Carolyn M. Brown Ph.D. Kenneth A. Lawson Ph.D. Karen L. Rascati Ph.D. James P. Wilson Ph.D. Mary Steinhardt Ed.D. L.P.C. |
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Affiliation: | aDepartment of Pharmaceutical, Social and Administrative Sciences, Appalachian College of Pharmacy, 1060 Dragon Road, Oakwood, VA 24631, USA;bPharmacy Administration Division, College of Pharmacy, The University of Texas at Austin, 1 University Station A1900 Austin, TX, USA;cDepartment of Kinesiology and Health Education, College of Education, The University of Texas at Austin, 1 University Station D3700 Austin, TX, USA |
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Abstract: |
BackgroundAdverse drug event (ADE) reporting by pharmacists is an indispensable part of the drug safety system. U.S. pharmacists may submit reports of serious ADEs that they encounter to the Food and Drug Administration (FDA) through MedWatch. However, underreporting of serious ADEs is a common problem. Little is known about pharmacists’ decision making with respect to ADE reporting.ObjectivesThis study explored the utility of the theory of planned behavior (TPB) model in predicting Texas pharmacists’ intention to report serious ADEs to the FDA.MethodsData were collected from practicing Texas pharmacists using a mail questionnaire. A total of 1500 surveys were mailed, and 377 usable responses were obtained for a response rate of 26.4%.ResultsA majority (70.2%) of the 377 respondents were white/Caucasian, and 52.9% were male. Overall, pharmacists intended to report serious ADEs (mean = 15.87 ± 4.22; possible range: 3-21), had a positive attitude toward reporting (mean = 4.62 ± 4.92; possible range: −15 to +15), perceived that important others wanted them to report (subjective norm [SN] score = 5.65 ± 2.99; possible range: −9 to +9), and believed that they had control over their reporting behavior (perceived behavioral control [PBC] score = 3.54 ± 2.69; possible/actual range: −6 to +6). Attitude (β = 0.221, P < .001) and SN (β = 0.438, P < .001) significantly predicted intent; however, PBC (β = 0.028, P > .05) did not. Attitude, SN, and PBC together accounted for 34.0% of the variance in intention to report serious ADEs (P < .001). The addition of past reporting behavior (P = .021) and perceived moral obligation (P < .001) significantly increased the variance in intention explained by the TPB model.ConclusionsPharmacists showed a strong positive intent to report serious ADEs to the FDA. Strategies to increase pharmacists’ intentions to report serious ADEs should focus on helping them see the value of reporting and altering their perception of social pressure toward reporting. The TPB may have utility in predicting ADE-reporting behavior. |
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Keywords: | Adverse drug events ADR reporting Pharmacists Attitude Drug and patient safety Pharmacovigilance Spontaneous reporting |
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