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Eugène van Puijenbroek

Researcher at University of Groningen

Publications -  177
Citations -  3773

Eugène van Puijenbroek is an academic researcher from University of Groningen. The author has contributed to research in topics: Pharmacovigilance & Adverse drug reaction. The author has an hindex of 27, co-authored 153 publications receiving 3042 citations. Previous affiliations of Eugène van Puijenbroek include University Medical Center Groningen & Radboud University Nijmegen.

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A comparison of measures of disproportionality for signal detection in spontaneous reporting systems for adverse drug reactions.

TL;DR: The objective of this study is to examine the level of concordance of the various estimates to the measure used by the WHO Collaborating Centre for International ADR monitoring, the information component (IC), when applied to the dataset of the Netherlands Pharmacovigilance Foundation Lareb.
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Comparative risk of major congenital malformations with eight different antiepileptic drugs: a prospective cohort study of the EURAP registry

Torbjörn Tomson, +135 more
- 01 Jun 2018 - 
TL;DR: Risks of major congenital malformation associated with lamotrigine, levetiracetam, and oxcarbazepine were within the range reported in the literature for offspring unexposed to antiepileptic drugs, and rational selection of these drugs is facilitated.
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The role of data mining in pharmacovigilance.

TL;DR: After a focused review of postapproval drug safety signal detection, the authors explain how the currently used algorithms work and address key questions related to their validation, comparative performance, deployment in naturalistic pharmacovigilance settings, limitations and potential for misuse.
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Use of measures of disproportionality in pharmacovigilance: three Dutch examples.

TL;DR: Three Dutch examples are described in which a measure of disproportionality is used in quantitative signal detection in pharmacovigilance, and it is concluded that the use of quantitative measures in addition to qualitative analysis is a step forward in signal Detection in pharmacvigilance.
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On the assessment of adverse drug reactions from spontaneous reporting systems: the influence of under-reporting on odds ratios

TL;DR: It is shown that certain under-reporting problems play no role in assessing ADRs from SRSs: the results from the analyses turn out to be biased by some specific under- reporting problems, but not by others.