BD (Becton, Dickinson and Company), notified customers that the U.S. Food and Drug Administration (FDA) has updated its March 2015 Safety Alert based on Teva Pharmaceuticals’ (Teva) findings which include that the BD PhaSeal™ System is the only closed system drug transfer device (CSTD) compatible with the chemotherapy drug, Treanda® Injection (bendamustine HCl) based on the testing performed by Teva from February through June 2015.
Consistent with all previous BD PhaSeal System testing, Teva’s independent studies confirmed the compatibility of the BD PhaSeal CSTD consisting of: BD PhaSeal Protector (P14), BD PhaSeal Injector (N35), and BD PhaSeal Infusion Adapter (C100). The raw materials used in the system are chosen for their chemical resistance and these products do not contain polycarbonate or ABS in the fluid path material shown to interact with hazardous drugs that contain the solvent N, N-Dimethylacetamide. In addition, Teva also identified the BD PhaSeal Secondary Set (C60) is compatible for IV administration of Treanda Injection.
Treanda is indicated for the treatment of patients with chronic lymphocytic leukemia (CLL) and bendamustine is recognized by the National Comprehensive Cancer Network (NCCN) as a first line therapy for CLL. The BD PhaSeal System is not contraindicated for any known hazardous drugs, including those that contain N, N-dimethylacetamide as a solvent.
“BD is committed to providing health care workers with the proper protection required to handle hazardous drugs that can help save the lives of patients in need,” said Lynne Kelley, MD, FACS, Vice President, Worldwide Medical Affairs, BD Medication & Procedural Solutions, BD Medical. “We are proud to offer one of the most comprehensive portfolios to empower protection of healthcare workers from hazardous drug exposure. Our goal is to help ensure that every patient around the world receives the necessary medication required for their specific treatment plan, without jeopardizing the health of the hospital workers who handle these hazardous drugs.”
BD shares the FDA’s focus on educating health care providers about the proper use of its products to ensure safe medication practices and the safe handling of hazardous drugs. Earlier this month, Teva Pharmaceuticals issued a letter to health care providers summarizing the compatibility results from their internal testing, which was immediately followed by an updated Safety Alert from the FDA confirming the compatibility between Treanda Injection and the BD PhaSeal System the only CSTD verified by Teva to be compatible with its chemotherapy drug.
BD (bd.com) is a leading medical technology company that partners with customers and stakeholders to address many of the world’s most pressing and evolving health needs. Our innovative solutions are focused on improving medication management and patient safety; supporting infection prevention practices; equipping surgical and interventional procedures; improving drug delivery; aiding anesthesiology and respiratory care; advancing cellular research and applications; enhancing the diagnosis of infectious diseases and cancers; and supporting the management of diabetes. We are more than 45,000 associates in 50 countries who strive to fulfill our purpose of “Helping all people live healthy lives” by advancing the quality, accessibility, safety and affordability of healthcare around the world. In 2015, BD welcomed CareFusion and its products into the BD family of solutions.