Zobrazeno 1 - 10
of 267
pro vyhledávání: '"Krämer Irene"'
Publikováno v:
Pharmaceutical Technology in Hospital Pharmacy, Vol 9, Iss 1, Pp 159-20 (2024)
Trastuzumab biosimilar SB3 (Ontruzant®), a HER2 binding monoclonal antibody, is available as powder for concentrate for solution for infusion. According to the summary of product characteristics, the reconstituted solution (21 mg/mL) is physicochemi
Externí odkaz:
https://doaj.org/article/c06b283f814f45c4baf5b75778435486
Publikováno v:
Pharmaceutical Technology in Hospital Pharmacy, Vol 8, Iss 1, Pp 709-19 (2023)
To date, there is only one study investigating the physicochemical stability of diluted mitomycin (MMC) solutions prepared by using urea-containing Mitomycin medac as starting material. The aim of the study was to test the solubility of the new MMC f
Externí odkaz:
https://doaj.org/article/6aa297c459ea4dd58ff643696b29b80c
Publikováno v:
Pharmaceutical Technology in Hospital Pharmacy, Vol 8, Iss 1, Pp 159-90 (2023)
Durvalumab (Imfinzi®), a PD-L1 monoclonal antibody (mAb) medication is available as concentrate (50 mg/mL) for solution for infusion. The summary of product characteristics provides information about the physicochemical stability of ready-to-adminis
Externí odkaz:
https://doaj.org/article/e6da5d4ac98c43488d929824c8a08c76
Publikováno v:
Pharmaceutical Technology in Hospital Pharmacy, Vol 6, Iss 1, Pp 265-80 (2021)
The objective of this study was to investigate the physicochemical stability of human insulin 1 I.U./mL injection solutions (Insuman® Rapid) diluted with 0.9% NaCl solution in 50 mL disposable three-piece polypropylene syringes and stored refrigerat
Externí odkaz:
https://doaj.org/article/44a2f18f6e254e0db508d475ea65a62d
Publikováno v:
Pharmaceutical Technology in Hospital Pharmacy, Vol 4, Iss 3-4, Pp 113-117 (2020)
In hospitals, the majority of medication therapy is administered intravenously. Especially, in intensive care units, simultaneous of various injectable drugs is a common practice Drug incompatibilities have been reported to be associated with up to 6
Externí odkaz:
https://doaj.org/article/a9440a0c4eb74736b8d581d1b92910fe
Publikováno v:
Pharmaceutical Technology in Hospital Pharmacy, Vol 7, Iss 1, Pp 798-9 (2022)
In adult intensive care patients, epinephrine is mostly administered by continuous injection with syringe pumps. The objective of this study was to investigate the physicochemical stability of pharmacy prepared ready-to-use epinephrine (E) 0.02 mg/mL
Externí odkaz:
https://doaj.org/article/53c7f657a6924d679f96a71aa362c4f0
Publikováno v:
Pharmaceutical Technology in Hospital Pharmacy, Vol 7, Iss 1, Pp 20210005-6 (2022)
The objective of this study was to investigate the physicochemical stability of ready-to-adminster human insulin (HI) 1 I.U./mL injection solutions of two different brand products diluted with 0.9% NaCl solution under different storage conditions eit
Externí odkaz:
https://doaj.org/article/42de032a12334159b0d7b91c21319f39
Autor:
Crauste-Manciet Sylvie, Krämer Irene, Lagarce Frederic, Sautou Valerie, Beaney Alison, Smith Julian, Fenton-May V’Iain, Hecq Jean-Daniel, Sadeghipour Farshid, Brun Paul Le
Publikováno v:
Pharmaceutical Technology in Hospital Pharmacy, Vol 5, Iss 1 (2020)
All dosage forms prepared in hospital pharmacies should be labelled with an appropriate shelf-life. This shelf-life should be validated taking chemical, physical and microbiological data into consideration. This guidance focuses on parenteral aseptic
Externí odkaz:
https://doaj.org/article/114b66ec1454416c894d687ec1a71ee3
Publikováno v:
Pharmaceutical Technology in Hospital Pharmacy, Vol 3, Iss 3, Pp 153-164 (2018)
Robotic systems are designed to minimize the exposure to antineoplastic drugs during automated preparation. However, contamination cannot be completely excluded. The aim of the study was to evaluate the contamination with antineoplastic drugs on the
Externí odkaz:
https://doaj.org/article/5151d80d431d46ffb97e435de4d28119
Publikováno v:
Pharmaceutical Technology in Hospital Pharmacy, Vol 2, Iss 4, Pp 145-157 (2017)
Profound knowledge about the physicochemical stability is necessary in order to determine the “beyond-use-dates” of ready-to-administer preparations after reconstitution and dilution. This is especially true for unstable azanucleoside drugs like
Externí odkaz:
https://doaj.org/article/20bb5f5d941b4395b6b99ea945352e23