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Sex differences in adverse drug reactions reported to the National Pharmacovigilance Centre in the Netherlands: An explorative observational study

British journal of clinical pharmacology, 2019-07, Vol.85 (7), p.1507-1515

2019

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Role of Drug–Gene Interactions and Pharmacogenetics in Simvastatin-Associated Pulmonary Toxicity

Drug safety, 2021-11, Vol.44 (11), p.1179-1191

2021

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Reported congenital malformations after exposure to non‐tumour necrosis factor inhibitor biologics: A retrospective comparative study in EudraVigilance

British journal of clinical pharmacology, 2022-12, Vol.88 (12), p.5378-5388

2022

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Body weight gain in clozapine‐treated patients: Is norclozapine the culprit?

British journal of clinical pharmacology, 2022-02, Vol.88 (2), p.853-857

2022

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Frequency and Acceptance of Clinical Decision Support System-Generated STOPP/START Signals for Hospitalised Older Patients with Polypharmacy and Multimorbidity

Drugs & aging, 2022-01, Vol.39 (1), p.59-73

2022

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Pharmacovigilance Skills, Knowledge and Attitudes in our Future Doctors – A Nationwide Study in the Netherlands

Basic & clinical pharmacology & toxicology, 2017-05, Vol.120 (5), p.475-481

2017

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Inhibition of CYP2D6 with low dose (5 mg) paroxetine in patients with high 10‐hydroxynortriptyline serum levels‐A prospective pharmacokinetic study

British journal of clinical pharmacology, 2021-03, Vol.87 (3), p.1529-1532

2021

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When More Is Less: An Exploratory Study of the Precautionary Reporting Bias and Its Impact on Safety Signal Detection

Clinical pharmacology and therapeutics, 2018-02, Vol.103 (2), p.296-303

2018

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Retroperitoneal fibrosis and β‐blocking agents: Is there an association?

British journal of clinical pharmacology, 2021-07, Vol.87 (7), p.2891-2901

2021

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Detectability of Medication Errors With a STOPP/START-Based Medication Review in Older People Prior to a Potentially Preventable Drug-Related Hospital Admission

Drug safety, 2022-12, Vol.45 (12), p.1501-1516

2022

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A prediction model‐based algorithm for computer‐assisted database screening of adverse drug reactions in the Netherlands

Pharmacoepidemiology and drug safety, 2018-02, Vol.27 (2), p.199-205

2018

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Validation of a Novel Method to Assess the Clinical Quality of Information in Pregnancy-Related Pharmacovigilance Case Reports: A ConcePTION Project

Drug safety, 2024-03, Vol.47 (3), p.261-270

2024

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Time to onset in statistical signal detection revisited: A follow‐up study in long‐term onset adverse drug reactions

Pharmacoepidemiology and drug safety, 2019-10, Vol.28 (10), p.1283-1289

2019

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Traceability of Biologics in The Netherlands: An Analysis of Information-Recording Systems in Clinical Practice and Spontaneous ADR Reports

Drug safety, 2016-02, Vol.39 (2), p.185-192

2016

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Tamsulosin Associated with Interstitial Lung Damage in CYP2D6 Variant Alleles Carriers

International journal of molecular sciences, 2020-04, Vol.21 (8), p.2770

2020

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Patient-Reported Adverse Events of Radiopharmaceuticals: Development and Validation of a Questionnaire

Drug safety, 2020-04, Vol.43 (4), p.319-328

2020

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Web-based questionnaires to assess perinatal outcome proved to be valid

Journal of clinical epidemiology, 2017-10, Vol.90, p.136-143

2017

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Safe use of radiopharmaceuticals in patients with chronic kidney disease: a systematic review

EJNMMI radiopharmacy and chemistry, 2021-08, Vol.6 (1), p.27-23, Article 27

2021

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Quality of Active versus Spontaneous Reporting of Adverse Drug Reactions in Pediatric Patients: Relevance for Pharmacovigilance and Knowledge in Pediatric Medical Care

Pharmaceuticals (Basel, Switzerland), 2022-09, Vol.15 (9), p.1148

2022

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Feasibility and Educational Value of a Student-Run Pharmacovigilance Programme: A Prospective Cohort Study

Drug safety, 2017-05, Vol.40 (5), p.409-418

2017

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Inhibition of CYP2D6 with low dose (5 mg) paroxetine in patients with high 10‐hydroxynortriptyline serum levels – a review of routine practice

British journal of clinical pharmacology, 2017-05, Vol.83 (5), p.1149-1151

2017

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The International Pharmacy Game: A Comparison of Implementation in Seven Universities World-Wide

Pharmacy, 2021-07, Vol.9 (3), p.125

2021

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Analysis of Reporting Adverse Drug Reactions in Paediatric Patients in a University Hospital in the Netherlands

Paediatric drugs, 2020-08, Vol.22 (4), p.425-432

2020

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Barriers and facilitators for systematically registering adverse drug reactions in electronic health records: a qualitative study with Dutch healthcare professionals

Expert opinion on drug safety, 2022-05, Vol.21 (5), p.699-706

2022

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Sex differences in adverse drug reactions reported to the National Pharmacovigilance Centre in the Netherlands: An explorative observational study

Role of Drug–Gene Interactions and Pharmacogenetics in Simvastatin-Associated Pulmonary Toxicity

Reported congenital malformations after exposure to non‐tumour necrosis factor inhibitor biologics: A retrospective comparative study in EudraVigilance

Body weight gain in clozapine‐treated patients: Is norclozapine the culprit?

Frequency and Acceptance of Clinical Decision Support System-Generated STOPP/START Signals for Hospitalised Older Patients with Polypharmacy and Multimorbidity

Pharmacovigilance Skills, Knowledge and Attitudes in our Future Doctors – A Nationwide Study in the Netherlands

Inhibition of CYP2D6 with low dose (5 mg) paroxetine in patients with high 10‐hydroxynortriptyline serum levels‐A prospective pharmacokinetic study

When More Is Less: An Exploratory Study of the Precautionary Reporting Bias and Its Impact on Safety Signal Detection

Retroperitoneal fibrosis and β‐blocking agents: Is there an association?

Detectability of Medication Errors With a STOPP/START-Based Medication Review in Older People Prior to a Potentially Preventable Drug-Related Hospital Admission

A prediction model‐based algorithm for computer‐assisted database screening of adverse drug reactions in the Netherlands

Validation of a Novel Method to Assess the Clinical Quality of Information in Pregnancy-Related Pharmacovigilance Case Reports: A ConcePTION Project

Time to onset in statistical signal detection revisited: A follow‐up study in long‐term onset adverse drug reactions

Traceability of Biologics in The Netherlands: An Analysis of Information-Recording Systems in Clinical Practice and Spontaneous ADR Reports

Tamsulosin Associated with Interstitial Lung Damage in CYP2D6 Variant Alleles Carriers

Patient-Reported Adverse Events of Radiopharmaceuticals: Development and Validation of a Questionnaire

Improving Data Collection in Pregnancy Safety Studies: Towards Standardisation of Data Elements in Pregnancy Reports from Public and Private Partners, A Contribution from the ConcePTION Project

Web-based questionnaires to assess perinatal outcome proved to be valid

Safe use of radiopharmaceuticals in patients with chronic kidney disease: a systematic review

Quality of Active versus Spontaneous Reporting of Adverse Drug Reactions in Pediatric Patients: Relevance for Pharmacovigilance and Knowledge in Pediatric Medical Care

Feasibility and Educational Value of a Student-Run Pharmacovigilance Programme: A Prospective Cohort Study

Inhibition of CYP2D6 with low dose (5 mg) paroxetine in patients with high 10‐hydroxynortriptyline serum levels – a review of routine practice

The International Pharmacy Game: A Comparison of Implementation in Seven Universities World-Wide

Analysis of Reporting Adverse Drug Reactions in Paediatric Patients in a University Hospital in the Netherlands

Barriers and facilitators for systematically registering adverse drug reactions in electronic health records: a qualitative study with Dutch healthcare professionals

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