4 results match your criteria: "and Purdue University College of Pharmacy[Affiliation]"

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Risk of Patient Harm Related to Unnecessary Dilution of Ready-to-Administer Prefilled Syringes: A Literature Review.

J Infus Nurs

February 2021

Regenstrief Center for Healthcare Engineering and Purdue University College of Pharmacy, West Lafayette, Indiana (Dr Degnan); University of Iowa Hospitals & Clinics, Iowa City, Iowa (Ms Bullard); University of Iowa Stead Family Children's Hospital (Ms Davis).

Unnecessary dilution of ready-to-administer (RTA) syringes could increase the risk of patient harm attributed to errors related to incorrect dose, improper labeling, and the potential for microbial contamination. Although published guidelines endorse the use of commercially available RTA syringes, recent surveys indicate that best practices are not always implemented. The purpose of this article is to review the existing literature and to assess the incidence and nature of errors related to the unnecessary dilution of RTA intravenous (IV) push medications in the inpatient clinical setting.

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Estimated Budget Impact of Increased Use of Mirabegron, A Novel Treatment for Overactive Bladder.

J Manag Care Spec Pharm

September 2016

4 Medical Affairs, Americas, Astellas Pharmaceutical Global Development, Northbrook, Illinois.

Background: Oral pharmacological treatment for overactive bladder (OAB) consists of antimuscarinics and the beta-3 adrenergic agonist mirabegron. Antimuscarinic adverse events (AEs) such as dry mouth, constipation, and blurry vision can result in frequent treatment discontinuation rates, leaving part of the OAB population untreated. Antimuscarinics also contribute to a patient's anticholinergic cognitive burden (ACB), so the Beers Criteria recommends cautious use of antimuscarinics in elderly patients who take multiple anticholinergic medications or have cognitive impairment.

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Objective: To establish preferred strategies for presenting drug-drug interaction (DDI) clinical decision support alerts.

Materials And Methods: A DDI Clinical Decision Support Conference Series included a workgroup consisting of 24 clinical, usability, and informatics experts representing academia, health information technology (IT) vendors, healthcare organizations, and the Office of the National Coordinator for Health IT. Workgroup members met via web-based meetings 12 times from January 2013 to February 2014, and two in-person meetings to reach consensus on recommendations to improve decision support for DDIs.

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