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Safe and effective pharmacotherapy in infants and preschool children: Importance of formulation aspects

  • Diana A. Van Riet-Nales*
  • , Alfred F A M Schobben
  • , Herman Vromans
  • , Toine C G Egberts
  • , Carin M A Rademaker
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

1 Citation (Scopus)
2 Downloads (Pure)

Abstract

Safe and effective paediatric pharmacotherapy requires careful evaluation of the type of drug substance, the necessary dose and the age-appropriateness of the formulation. Generally, the younger the child, the more the attention that is required. For decades, there has been a general lack of (authorised) formulations that children are able to and willing to take. Moreover, little was known on the impact of pharmaceutical aspects on the age-appropriateness of a paediatric medicine. As a result of legislative incentives, such knowledge is increasingly becoming available. It has become evident that rapidly dissolving tablets with a diameter of 2mm (mini-tablets) can be used in preterm neonates and non-rapidly dissolving 2mm mini-tablets in infants from 6months of age. In addition, uncoated 4mm mini-tablets can be used in infants from the age of 1year. Also, there is some evidence that children prefer mini-tablets over a powder, suspension or syrup. Other novel types of age-appropriate oral formulations such as orodispersible films may further add to the treatment possibilities. This review provides an overview of the current knowledge on oral formulations for infants and preschool children, the advantages and disadvantages of the different types of dosage forms and the age groups by which these can likely be used.

Original languageEnglish
Pages (from-to)662-669
Number of pages8
JournalArchives of Disease in Childhood
Volume101
Issue number7
DOIs
Publication statusPublished - 1 Jul 2016

Keywords

  • administration, oral
  • child
  • formulation
  • mini-tablet
  • tehnology, pharmaceutical

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