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Center of Healthcare Quality Assessme... 1 Department of Drug Management Faculty... 1 Department of Organisation and Manage... 1 Department of Social and Clinical Pha... 1 Egis Pharmaceuticals Budapest Hungary 1 Faculty of Pharmacy Medical Universit... 1 Kazakh Agency for Health Technology A... 1 Management Center Innsbruck Innsbruck... 1 Syreon Research Institute Budapest Hu... 1 Syreon Research Institute Budapest Hu... 1 Syreon Research Romania Tirgu Mures R... 1
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- Zeměpisné označení
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- Autor
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Pracoviště
Center of Healthcare Quality Assessme... 1 Department of Drug Management Faculty... 1 Department of Organisation and Manage... 1 Department of Social and Clinical Pha... 1 Egis Pharmaceuticals Budapest Hungary 1 Faculty of Pharmacy Medical Universit... 1 Kazakh Agency for Health Technology A... 1 Management Center Innsbruck Innsbruck... 1 Syreon Research Institute Budapest Hu... 1 Syreon Research Institute Budapest Hu... 1 Syreon Research Romania Tirgu Mures R... 1
- Formát
- Publikační typ
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- Kategorie
- Zeměpisné označení
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- Země
- Časopis/zdroj
- Dostupnost
- Vlastník
Kostyuk, Alexander* Dotaz Zobrazit nápovědu
NLK
Free Medical Journals
od 2013
Hindawi Publishing Open Access
od 2001-01-01
PubMed Central
od 2013
Europe PubMed Central
od 2013
ProQuest Central
od 2013
Open Access Digital Library
od 2001-01-01
Open Access Digital Library
od 2012-12-04
Open Access Digital Library
od 2013-01-01
CINAHL Plus with Full Text (EBSCOhost)
od 2013-01-01
Medline Complete (EBSCOhost)
od 2013-01-01
Health & Medicine (ProQuest)
od 2013
ROAD: Directory of Open Access Scholarly Resources
od 2013
PubMed
29546072
DOI
10.1155/2018/9597362
Knihovny.cz E-zdroje
This policy research aims to map patient access barriers to biologic treatments, to explore how increased uptake of biosimilars may lower these hurdles and to identify factors limiting the increased utilisation of biosimilars. A policy survey was developed to review these questions in 10 Central and Eastern European (CEE) and Commonwealth of Independent States (CIS) countries. Two experts (one public and one private sector representative) from each country completed the survey. Questions were related to patient access, purchasing, clinical practice, and real-world data collection on both original biologics and biosimilars. Restrictions on the number of patients that can be treated and related waiting lists were reported as key patient access barriers. According to respondents, for both clinicians and payers the primary benefit of switching patients to biosimilars would be to treat more patients. However, concerns with therapeutic equivalence and fear of immunogenicity may reduce utilisation of biosimilars. Similar limitations in patient access to both original biologics and biosimilars raise concerns about the appropriateness and success of current biosimilar policies in CEE and CIS countries. The conceptual framework for additional real-world data collection exists in all countries which may provide a basis for future risk-management activities including vigorous pharmacovigilance data collection.
- MeSH
- biosimilární léčivé přípravky škodlivé účinky terapeutické užití MeSH
- farmakovigilance MeSH
- lidé MeSH
- průzkumy a dotazníky MeSH
- Společenství nezávislých států epidemiologie MeSH
- terapeutická ekvivalence * MeSH
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- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Geografické názvy
- Společenství nezávislých států epidemiologie MeSH
- východní Evropa epidemiologie MeSH
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