Literature DB >> 24398969

The impact of legislation on drug substances used off-label in paediatric wards--a nationwide study.

Sissel Haslund-Krog1, René Mathiasen, Hanne Rolighed Christensen, Helle Holst.   

Abstract

PURPOSE: This nationwide study is aimed at describing to what extent the European Paediatric Regulation has met therapeutic needs in children.
METHODS: Data for each drug substance in defined daily doses (DDD) were extracted from the national Danish data base. We evaluated if drug substances were used off-label and whether they had a paediatric investigation plan (PIP). This study did not include drug prescriptions for individual paediatric patients; thus, it was not possible to make use of all off-label categories previously used. Additionally, paediatric standard assortments (SA) were compared to the European survey on paediatric medicinal products.
RESULTS: Thirteen percent of the 100 most used drug substances were determined as being used off-label, four of which had a PIP and one had a full waiver. Only one of the three drug substances used off-label most often, accounting for 85 % of such use, had a PIP. Neonates were included in one-third of PIPs and adolescents in 15. Nineteen out of 21 PIPs had a waiver and 14 PIPs were deferred. In line with the European survey, carbapenems, corticosteroids and proton pump inhibitors were frequent found in SAs.
CONCLUSION: PIPs only cover a small proportion of the drugs found to be used off-label in this study. Despite waivers granted, drug substances were used nonetheless. Unmet regulatory needs are still considerable in some therapeutic areas in neonates as well as in children.

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Mesh:

Year:  2014        PMID: 24398969     DOI: 10.1007/s00228-013-1626-1

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


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