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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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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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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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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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Burden of non-serious infections during biological use for rheumatoid arthritis

PloS one, 2024-02, Vol.19 (2), p.e0296821-e0296821

2024

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Optimizing Safety Surveillance for COVID-19 Vaccines at the National Pharmacovigilance Centre Lareb: One Year of COVID-19 Vaccine Experience

Drug safety, 2023-01, Vol.46 (1), p.65-75

2023

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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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Nivel Corona Cohort: A description of the cohort and methodology used for combining general practice electronic records with patient reported outcomes to study impact of a COVID-19 infection

PloS one, 2023-08, Vol.18 (8), p.e0288715-e0288715

2023

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The validity and reliability of a signal impact assessment tool

Pharmacoepidemiology and drug safety, 2016-07, Vol.25 (7), p.815-819

2016

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Does patient reporting lead to earlier detection of drug safety signals? A retrospective comparison of time to reporting between patients and healthcare professionals in a global database

British journal of clinical pharmacology, 2018-07, Vol.84 (7), p.1514-1524

2018

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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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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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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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The Quality of Clinical Information in Adverse Drug Reaction Reports by Patients and Healthcare Professionals: A Retrospective Comparative Analysis

Drug safety, 2017-07, Vol.40 (7), p.607-614

2017

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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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Evaluation of pharmacovigilance systems for reporting medication errors in Africa and the role of patients using a mixed-methods approach

PloS one, 2022-03, Vol.17 (3), p.e0264699-e0264699

2022

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The Impact of Experiencing Adverse Drug Reactions on the Patient’s Quality of Life: A Retrospective Cross-Sectional Study in the Netherlands

Drug safety, 2016-08, Vol.39 (8), p.769-776

2016

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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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Adverse drug reaction reports of patients and healthcare professionals-differences in reported information

Pharmacoepidemiology and drug safety, 2015-02, Vol.24 (2), p.152-158

2015

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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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Vitamin B 6 in Health Supplements and Neuropathy: Case Series Assessment of Spontaneously Reported Cases

Drug safety, 2018-09, Vol.41 (9), p.859

2018

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Peer Review in Pharmacovigilance: Lens on Disproportionality Analysis

Drug safety, 2024-07, Vol.47 (7), p.601-605

2024

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

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

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

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

Burden of non-serious infections during biological use for rheumatoid arthritis

Optimizing Safety Surveillance for COVID-19 Vaccines at the National Pharmacovigilance Centre Lareb: One Year of COVID-19 Vaccine Experience

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

Nivel Corona Cohort: A description of the cohort and methodology used for combining general practice electronic records with patient reported outcomes to study impact of a COVID-19 infection

The validity and reliability of a signal impact assessment tool

Does patient reporting lead to earlier detection of drug safety signals? A retrospective comparison of time to reporting between patients and healthcare professionals in a global database

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

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

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

The Quality of Clinical Information in Adverse Drug Reaction Reports by Patients and Healthcare Professionals: A Retrospective Comparative Analysis

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

Evaluation of pharmacovigilance systems for reporting medication errors in Africa and the role of patients using a mixed-methods approach

The Impact of Experiencing Adverse Drug Reactions on the Patient’s Quality of Life: A Retrospective Cross-Sectional Study in the Netherlands

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

Adverse drug reaction reports of patients and healthcare professionals-differences in reported information

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

Vitamin B 6 in Health Supplements and Neuropathy: Case Series Assessment of Spontaneously Reported Cases

Peer Review in Pharmacovigilance: Lens on Disproportionality Analysis

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

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