Container closure integrity testing and process validation of closed system transfer devices for aseptic reconstitution of drug vials connected to fluid bags-Reference-Cited by-同舟云学术

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Container closure integrity testing and process validation of closed system transfer devices for aseptic reconstitution of drug vials connected to fluid bags

Published:2023-02-15 Issue: Volume: Page:ejhpharm-2022-003604
ISSN:2047-9956
Container-title:European Journal of Hospital Pharmacy
language:en
Short-container-title:Eur J Hosp Pharm

Author:

van den Berg Roland B^ORCID,Akgöl Kübra,Swart Eleonora L,Nuijen Bastiaan,Crul Mirjam

Publisher

BMJ

Subject

General Pharmacology, Toxicology and Pharmaceutics

Reference24 articles.

1. Vossen MG , Milacek C , Thalhammer F . Empirical antimicrobial treatment in haemato-/oncological patients with neutropenic sepsis. ESMO Open 2018;3:e000348. doi:10.1136/esmoopen-2018-000348

2. Pfizer . Summary of product characteristics meronem i.v. 500 mg, powder for solution for injection or infusion. 2019. Available: https://www.cbg-meb.nl [Accessed 21 Jan 2023].

3. Manning L , Wright C , Ingram PR , et al . Continuous infusions of meropenem in ambulatory care: clinical efficacy, safety and stability. PLoS One 2014;9:e102023. doi:10.1371/journal.pone.0102023

4. Stability of meropenem in intravenous solutions;Patel;Am J Health-Syst Pharm,1997

5. Stability of Generic Meropenem Solutions for Administration by Continuous Infusion at Normal and Elevated Temperatures

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