Resolution CM/Res(2016)2 and Centralised Intra Venous Additive Services (CIVAS): Challenges and Opportunities

Autor: Vrignaud Sandy

Publikováno v: Pharmaceutical Technology in Hospital Pharmacy, Vol 2, Iss 3, Pp 137-142 (2017)

The aim of the European Council’s Resolution CM/res(2016)2 on good reconstitution practices in health care establishments for medicinal products for parenteral use is to guide the health care establishment’s decision as to where reconstitution sh

Externí odkaz: https://doaj.org/article/96697bd0f7a341e1a5c18d230d3dacac

Long-term physico-chemical stability of 5-fluorouracile at standardised rounded doses (SRD) in MyFuser® portable infusion pump

Autor: Benoît Bihin, Marie-Lise Colsoul, Laura Soumoy, M Closset, Jacques Jamart, Jean-Daniel Hecq, Laurence Galanti, Nicolas Goderniaux, Sabrina Onorati, Pascal Odou

Publikováno v: Journal of chemotherapy, Vol. 33, no. 7, p. 486-491 (2021)

Management of chemotherapies is a strategic issue for european healthcare. Dose-banding enables to reduce waiting time of patients in day care units and drug wastage. The aim of this study was to assess the stability of 5-Fluorouracile (5-FU) at stan

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3734ce796f64ffda51ffda170c6a28e
https://doi.org/10.1080/1120009x.2021.1906037

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Criteria for Judging the Quality of a Publication on Physicochemical Stability of Ready to Use Injectable Drugs

Autor: Jacques Jamart, Benoît Bihin, Laurence Galanti, Jean-Daniel Hecq

Publikováno v: Hecq, J-D, Bihin, B, Jamart, J & Galanti, L 2017, ' Criteria for Judging the Quality of a Publication on Physicochemical Stability of Ready to Use Injectable Drugs ', Pharmaceutical Technology in Hospital Pharmacy, vol. 2, no. 2 . https://doi.org/10.1515/pthp-2017-0012
Pharmaceutical Technology in Hospital Pharmacy, Vol 2, Iss 2, Pp 79-84 (2017)

In hospitals, a major part of the drugs is administered via the intravenous route. When one wants to evaluate or know the stability of a drug in solution, it is necessary to know several physico-chemical parameters. Several reference works are availa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24e0014542b74aca9aee90c9abd3cebc
https://pure.unamur.be/ws/files/53091374/_5B2365242X_20_20Pharmaceutical_20Technology_20in_20Hospital_20Pharmacy_5D_20Criteria_20for_20Judging_20the_20Quality_20of_20a_20Publication_20on_20Physicochemical_20Stability_20of_20Ready_20to_20Use_20Injectable_20Drugs.pdf

Stability of micafungin sodium solutions at different concentrations in glass bottles and syringes

Autor: Thomas Briot, Frédéric Lagarce, Sandy Vrignaud

Publikováno v: International Journal of Pharmaceutics
International Journal of Pharmaceutics, Elsevier, 2015, 492, pp.137-40. ⟨10.1016/j.ijpharm.2015.07.019⟩

International audience; Micafungin is a costly treatment and packaging of 50mg or 100mg bottles only are available, while doses lower than 5mg and 20mg are often necessary in neonates and paediatrics patients, respectively. The stability of micafungi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b6c1e48b4dab54a0cc2cb7f62941769
https://hal.archives-ouvertes.fr/hal-01392457