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Wiley InterScience

British Journal of Clinical Pharmacology

British Journal of Clinical Pharmacology

Volume 59 Issue 6, Pages 677 - 683

Published Online: 7 Jun 2005

Journal compilation © 2010 The British Pharmacological Society



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Monitoring adverse drug reactions in children using community pharmacies: a pilot study
Derek Stewart 2 , Peter Helms 1 , Dorothy McCaig 2 , Christine Bond 3 & James McLay 4
  4 Department of Medicine and Therapeutics, University of Aberdeen,   1 Department of Child Health, University of Aberdeen, Royal Aberdeen Children's Hospital Foresterhill,   2 School of Pharmacy, The Robert Gordon University, and   3 Department of General Practice and Primary Care, University of Aberdeen, Aberdeen, UK
Correspondence to  Dr James McLay, Department of Medicine and Therapeutics, The University of Aberdeen, Polwarth Buildings, Foresterhill, Aberdeen AB25 2ZD, UK. Tel.: + 44 (0)1224 55 3015 E-mail: j.mclay@abdn.ac.uk
Copyright 2005 Blackwell Publishing Ltd
KEYWORDS
adverse drug reactions • children • community • parental • pharmacy • questionnaire

ABSTRACT

Aims  To determine the feasibility of a community pharmacy-based parental adverse drug reaction (ADR) reporting system for children.

Design  Prospective study of parent-reported ADRs using a questionnaire issued to the parent or guardians of children 0–11 years of age collecting prescribed medicine for amoxicillin, and/or salbutamol, and collecting prescribed medicine for, or purchasing, paracetamol or ibuprofen suspension.

Setting  Seven community pharmacies in Grampian, Scotland.

Results  During a 4-week period 360 prescriptions or purchases for the study medications occurred. Two hundred and sixty-seven parents (85.5%) agreed to participate in the study. One hundred and six participants (40%) returned a total of 122 questionnaires. The demographics of responders and nonresponders including medication, age of child, and social status as assessed by the Depcat score were similar. There was no evidence of under-representation of any socio-economic group. Possible adverse events were detected using a symptom tick list and perceived ADRs using free text entry. Using the symptom tick list approach the most commonly reported symptoms were diarrhoea (28.9%) and tiredness (31.6%) for amoxicillin. The levels of diarrhoea and tiredness reported for ibuprofen, paracetamol and salbutamol were 15% and 20%, 7.4% and 18.5%, and 20% and 0%, respectively. Using the freehand section of the questionnaire 15 specific ADRs were reported by parents (12.3%). Eight children (21.2%) reported ADRs attributed to amoxicilin [diarrhoea (n = 4), fever (n = 1), anorexia (n = 1), hyperactivity (n = 1) and nonspecific (n = 1)], five to paracetamol [diarrhoea (n = 3), anorexia, irritability, crying and very angry (n = 1) and not stated (n = 1)], two to ibuprofen [diarrhoea (n = 1), not stated (n = )]. Only one off-label prescription was identified and this was for salbutamol syrup prescribed to a child under 2 years of age.

Conclusions  The prospective monitoring of paediatric ADRs, using a questionnaire issued to parents or guardians in the community pharmacies, is feasible.


Received 31 January 2005 Accepted 16 February 2005

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1365-2125.2005.02424.x About DOI

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