Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Judith Thiesen"'
Publikováno v:
Pharmaceutics, Vol 15, Iss 2, p 309 (2023)
The objective of this study was to determine the physicochemical in-use stability of recently approved Thiotepa Riemser concentrate in the original vial and diluted ready-to-administer (RTA) infusion solutions in prefilled glucose 5% and 0.9% NaCl po
Externí odkaz:
https://doaj.org/article/5b58eb8acc62497fade54ca2f12597d6
Physicochemical stability of ready-to-administer mitomycin C solutions for intravesical instillation
Publikováno v:
European Journal of Hospital Pharmacy. :ejhpharm-2023
Publikováno v:
European Journal of Hospital Pharmacy. 30:11-16
Introduction The aim of this study was to determine and compare the physicochemical stability of two carmustine-containing medicinal products licensed and marketed in Europe as Carmustin Obvius (Medac GmbH) and Carmubris (Tillomed Pharma GmbH). Recon
Publikováno v:
Pharmaceutical research. 37(8)
Monoclonal antibody (Mabs) containing medicinal products are widely used in clinical practice. Prior to parenteral administration, licensed Mab containing medicinal products are transferred to the ready-to-administer (RTA) forms. Reconstitution and/o
Stability of Ready-to-Administer and Ready-to-Use Epinephrine and Norepinephrine Injection Solutions
Publikováno v:
Pharmaceutical Technology in Hospital Pharmacy, Vol 2, Iss 4, Pp 159-171 (2017)
BackgroundIn the University Medical Centre Mainz, standard concentrations are defined for medicinal products to be administered by continuous injection with syringe pumps in adult intensive care patients. The objective of this study was to evaluate t
Publikováno v:
European Journal of Hospital Pharmacy. 22:260-266
Objectives This study was conducted to investigate the extended physicochemical stability of cabazitaxel containing premix solution and diluted infusion solutions in either 0.9% sodium chloride (NaCl) or 5% glucose (G5) vehicle solution. Methods A st
Publikováno v:
Journal of Oncology Pharmacy Practice. 22:195-204
Objective The purpose of this study was to evaluate the contamination rate of media-fill products either prepared automated with a robotic system (APOTECAchemo™) or prepared manually at cytotoxic workbenches in the same cleanroom environment and by
Publikováno v:
Pharmaceutical Technology in Hospital Pharmacy, Vol 1, Iss 1, Pp 9-20 (2016)
Numerous ready-to-use parenteral solutions are aseptically prepared in pharmacy-based aseptic preparation units. Microbiological stability of the preparations is influenced by the cleanroom environment, the complexity of the aseptic process, conditio
Publikováno v:
Pharmaceutical Technology in Hospital Pharmacy, Vol 1, Iss 2, Pp 73-81 (2016)
The stability of ready-to-administer parenteral preparations is an important issue of drug safety. Profound knowledge about the physicochemical stability is necessary in order to determine the “beyond-use-dates” of solutions in injection vials af
Publikováno v:
Journal of Oncology Pharmacy Practice. 16:53-61
Purpose. The aim of this study was to determine the loading efficiency, physicochemical stability, and release of irinotecan-loaded DC BeadsTM (bead size 100—300 μm, 300—500 μm) before and after mixing with nonionic contrast medium (Accupaque®