Recurrence of adverse drug reactions following inappropriate re-prescription: better documentation, availability of information and monitoring are needed.

Translated title of the contribution: Recurrence of adverse drug reactions following inappropriate re-prescription: better documentation, availability of information and monitoring are needed.

C.M.J. van der Linden, P.A.F. Jansen, R.J. van Marum, R.J.E. Grouls, E.H.M. Korsten, A.C.G. Egberts

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Adverse drug reactions (ADRs) are a common, and often preventable, cause of hospital admission, especially in the elderly, and can occur during hospitalization. In this current opinion article, we present three cases of recurrence of a serious ADR due to re-prescription of a withdrawn medication that highlight the need for a system to prevent the undesirable re-prescription of medications withdrawn because of an ADR. In addition, we describe an electronic system that could help prevent undesirable re-prescription following an ADR. Such a system should document ADRs systematically at the patient level, make this information available to relevant healthcare providers and the patient, and flag re-prescription of the offending drug. The effectiveness and cost effectiveness of such a system would need to be determined.
Translated title of the contributionRecurrence of adverse drug reactions following inappropriate re-prescription: better documentation, availability of information and monitoring are needed.
Original languageUndefined/Unknown
Pages (from-to)535-8
Number of pages4
JournalDrug Safety
Volume33
Issue number7
Publication statusPublished - 2010

Keywords

  • Farmacie/Biofarmaceutische wetenschappen (FARM)
  • Epidemiology
  • Farmacie(FARM)
  • Biomedische technologie en medicijnen
  • Ziekenhuisstructuur en organisatie van de gezondheidszorg
  • Public Health

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