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Archives of Disease in Childhood 2006;91:550-551; doi:10.1136/adc.2006.094805
Copyright © 2006 BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health.

PERSPECTIVES

Children's medicines

Improving children’s medicines

I Choonara

Correspondence to:
Correspondence to:
Professor Imti Choonara
Academic Division of Child Health, University of Nottingham, Derbyshire Children’s Hospital, Derby, UK; imti.choonara@nottingham.ac.uk


Perspective on the paper by McLay et al (see page584)

Keywords: medicines; licensing; clinical trials

The first 150 words of the full text of this article appear below.

It is reassuring that the majority of Scottish paediatricians are aware of the concept of off label prescribing (p XXX).1 The term off label relates to the use of a medicine in a manner different from that recommended by the manufacturers in their product licence.2 A formal classification system for the different types of off label and unlicensed drug use was described in 1997. In a period of a few years, several studies confirmed that off label drug prescribing was a significant problem in children in hospital,3 in neonates,4 and in primary care.5

The main reason for carrying out these epidemiological studies was to highlight the fact that medicines used in children have not been scientifically evaluated to the same extent as those used in adults.6,7 Groups such as the European Network for Drug Investigation in Children have highlighted that this is a problem in different . . . [Full text of this article]


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A prospective questionnaire assessment of attitudes and experiences of off label prescribing among hospital based paediatricians
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