CHALLENGES IN PEDIATRIC FORMULATIONS DEVELOPMENT: A REVIEW
Ambadas R. Chikkale* and Rajesh Kumar Nema
Abstract
Drug formulations used in pediatric pharmacotherapy should be
adapted to children‟s needs to suit their age, size, physiologic
condition, and treatment requirements. Such pediatric medicines are
keys to achieving safe and accurate dose administration, reducing the
risk of medication errors, enhancing medication adherence, and
improving therapeutic outcomes in children. The use of inadequate
drug formulations in children may pose problems not seen in adults,
such as difficulty in swallowing, safety issues with certain excipients
that are acceptable in adult formulations and adherence problems with
unpalatable medicines. Only a small fraction of all marketed drugs are
available in formulations that are age appropriate and suitable for
pediatric use. As a result, many adult medicines are used off-label in children, a practice that
carries additional health and environmental risks. A number of innovative pediatric
formulations have followed, but their actual effect on pediatric drug approvals remains to be
seen, as clinical trials and marketing authorization take a substantial amount of time. To
optimize pharmacotherapy in children, it is important for clinicians to understand the
background of the aforementioned problems as well as to gain insight into the challenges,
developments, and potential solutions. The aim of the present study was to describe specific
challenges for pediatric drug formulations and to address the absence of adequate availability
palatable formulations for children. We will discuss the major challenges in pediatric
formulation and development, role of acceptable palatability in achieving adherence of
pediatric population for pharmacotherapy and getting maximum outputs, the necessity of
pediatric formulations and future steps.
Keywords: Pediatric Formulations, Challenges in Pediatric formulations.
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