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Most cited papers from Netherlands Pharmacovigilance Centre Lareb

Netherlands Pharmacovigilance Centre Lareb

What are the most cited papers from Netherlands Pharmacovigilance Centre Lareb?

The most cited paper from Netherlands Pharmacovigilance Centre Lareb is "A comparison of measures of disproportionality for signal detection in spontaneous reporting systems for adverse drug reactions" (Eugène van Puijenbroek, Andrew M. Bate, Hubert G.M. Leufkens et al., 2002), with 1,385 citations. Next come "Medication use in pregnancy: a cross-sectional, multinational web-based study" (512) and "The REporting of A Disproportionality Analysis for DrUg Safety Signal Detection Using Individual Case Safety Reports in PharmacoVigilance (READUS-PV): Explanation and Elaboration" (332).

Showing 50 of 59 papers. Every paper with more than 71 citations is listed.

Most cited papers, sortable by citations and release date
#Paper
1 A comparison of measures of disproportionality for signal detection in spontaneous reporting systems for adverse drug reactions Eugène van Puijenbroek, Andrew M. Bate, Hubert G.M. Leufkens et al. · Pharmacoepidemiology and Drug Safety 2002 1,385
2 Medication use in pregnancy: a cross-sectional, multinational web-based study Angela Lupattelli, Olav Spigset, Michael James Twigg et al. · BMJ Open Open access Feb 2014 512
3 The REporting of A Disproportionality Analysis for DrUg Safety Signal Detection Using Individual Case Safety Reports in PharmacoVigilance (READUS-PV): Explanation and Elaboration Michele Fusaroli et al. · Drug Safety Open access 7 May 2024 332
4 Pharmacovigilance: methods, recent developments and future perspectives Linda Härmark, A.C. van Grootheest · European Journal of Clinical Pharmacology 3 Jun 2008 297
5 Attitudinal survey of voluntary reporting of adverse drug reactions Eland, Belton, van Adrianus Grootheest et al. · British Journal of Clinical Pharmacology Open access Oct 1999 257
6 The Reporting of a Disproportionality Analysis for Drug Safety Signal Detection Using Individual Case Safety Reports in PharmacoVigilance (READUS-PV): Development and Statement Michele Fusaroli et al. · Drug Safety Open access 7 May 2024 242
7 Causal or Casual? Ronald H.B. Meyboom, Yechiel A. Hekster, Toine C. G. Egberts et al. · Drug Safety Dec 1997 241
8 Principles of Signal Detection in Pharmacovigilance Ronald H.B. Meyboom, Toine C. G. Egberts, Ivor Ralph Edwards et al. · Drug Safety Jun 1997 238
9 Mental health status of pregnant and breastfeeding women during the COVID‐19 pandemic—A multinational cross‐sectional study Michael Ceulemans, Veerle Foulon, Elin Ngo et al. · Acta Obstetricia Et Gynecologica Scandinavica Open access 21 Jan 2021 219
10 Pregnancy Outcome After Methotrexate Treatment for Rheumatic Disease Prior to or During Early Pregnancy: A Prospective Multicenter Cohort Study Corinna Weber‐Schoendorfer et al. · Arthritis & Rheumatology 27 Jan 2014 209
11 Adverse Drug Reaction-Related Hospitalisations Cornelis S. Van Der Hooft, Miriam Sturkenboom, Kees van Grootheest et al. · Drug Safety Open access 2006 188
12 Adverse Drug Reaction Reporting by Patients in the Netherlands Joyce de Langen, Florence P. A. M. van Hunsel, Anneke Passier et al. · Drug Safety 2008 181
13 Pharmacists' role in reporting adverse drug reactions in an international perspective Kees van Grootheest, Sten Olsson, Mary Couper et al. · Pharmacoepidemiology and Drug Safety 15 Sep 2003 174
14 Sex differences in adverse drug reactions reported to the National Pharmacovigilance Centre in the Netherlands: An explorative observational study Sieta T. de Vries, Petra Denig, Corine Ekhart et al. · British Journal of Clinical Pharmacology Open access 3 Apr 2019 153
15 Use of Measures of Disproportionality in Pharmacovigilance Toine C. G. Egberts, Ronald H.B. Meyboom, Eugène van Puijenbroek · Drug Safety 2002 153
16 Adverse drug reactions to tocolytic treatment for preterm labour: prospective cohort study Roel de Heus, Ben W. Mol, J.J.H.M. Erwich et al. · BMJ Open access 5 Mar 2009 148
17 Application of Quantitative Signal Detection in the Dutch Spontaneous Reporting System for Adverse Drug Reactions Eugène van Puijenbroek, Willem L. Diemont, Kees van Grootheest · Drug Safety 2003 147
18 Fever as an adverse event following immunization: case definition and guidelines of data collection, analysis, and presentation S. Michael Marcy, Katrin S. Kohl, Ron Dagan et al. · Vaccine 14 Oct 2003 146
19 Experiences with Adverse Drug Reaction Reporting by Patients Florence P. A. M. van Hunsel, Linda Härmark, Shanthi Narayan Pal et al. · Drug Safety Open access 8 Dec 2011 145
20 Pharmacovigilance in Perspective Ronald H.B. Meyboom, Toine C. G. Egberts, Frank W.J. Gribnau et al. · Drug Safety 1999 144
21 An ABC of Drug-Related Problems Ronald H.B. Meyboom, Marie Lindquist, Toine C. G. Egberts · Drug Safety 2000 137
22 On the assessment of adverse drug reactions from spontaneous reporting systems: the influence of under‐reporting on odds ratios P.G.M. van der Heijden, Eugène van Puijenbroek, Stef van Buuren et al. · Statistics in Medicine Open access 19 Jun 2002 136
23 Medications and addictive substances potentially inducing or attenuating sleep bruxism and/or awake bruxism Cees De Baat, Merel Charlotte Verhoeff, Jari Ahlberg et al. · Journal of Oral Rehabilitation Open access 27 Jul 2020 132
24 Detecting drug–drug interactions using a database for spontaneous adverse drug reactions: an example with diuretics and non-steroidal anti-inflammatory drugs Eugène van Puijenbroek, Toine C. G. Egberts, Eibert Roelof Heerdink et al. · European Journal of Clinical Pharmacology 7 Nov 2000 130
25 Drug-Associated Acute Pancreatitis: Twenty-One Years of Spontaneous Reporting in The Netherlands Ingo A. Eland, Eugène van Puijenbroek, Miriam Sturkenboom et al. · The American Journal of Gastroenterology Open access Sep 1999 130
26 Guidelines for Submitting Adverse Event Reports for Publication William N. Kelly, Felix M Arellano, Joanne Barnes et al. · Drug Safety Open access 2007 129
27 Risk of candidiasis associated with interleukin-17 inhibitors: A real-world observational study of multiple independent sources Linda Davidson, Juul M. P. A. van den Reek, Mariolina Bruno et al. · The Lancet Regional Health - Europe Open access 22 Nov 2021 127
28 Signalling possible drug–drug interactions in a spontaneous reporting system: delay of withdrawal bleeding during concomitant use of oral contraceptives and itraconazole Eugène van Puijenbroek, Toine C. G. Egberts, Ronald H.B. Meyboom et al. · British Journal of Clinical Pharmacology Open access Jun 1999 124
29 Vaccine Willingness and Impact of the COVID-19 Pandemic on Women’s Perinatal Experiences and Practices—A Multinational, Cross-Sectional Study Covering the First Wave of the Pandemic Michael Ceulemans, Veerle Foulon, Alice Panchaud et al. · International Journal of Environmental Research and Public Health Open access 24 Mar 2021 118
30 Pregnancy outcome following maternal exposure to statins: a multicentre prospective study Ursula Winterfeld, Arthur Allignol, Alice Panchaud et al. · BJOG An International Journal of Obstetrics & Gynaecology 30 Nov 2012 118
31 Can adverse drug reactions be detected earlier? A comparison of reports by patients and professionals: Fig 1 Toine C. G. Egberts, Maartje Smulders, Fred H.P. De Koning et al. · BMJ Open access 31 Aug 1996 117
32 Performance and safety of an integrated bihormonal artificial pancreas for fully automated glucose control at home Helga Blauw, Arianne C. van Bon, Renata Koops et al. · Diabetes Obesity and Metabolism Open access 21 Mar 2016 116
33 Consumer Adverse Drug Reaction Reporting Kees van Grootheest, Linda de Graaf, Lolkje T.W. de Jong‐van den Berg · Drug Safety 2003 115
34 The role of hospital and community pharmacists in pharmacovigilance A.C. van Grootheest, Lolkje T.W. de Jong‐van den Berg · Research in Social and Administrative Pharmacy Mar 2005 108
35 Proton pump inhibitor‐induced acute interstitial nephritis Linda Härmark, Hans E. van der Wiel, Mark de Groot et al. · British Journal of Clinical Pharmacology Open access 17 Jul 2007 105
36 Metamizole (Dipyrone) as an Alternative Agent in Postoperative Analgesia in Patients with Contraindications for Nonsteroidal Anti‐Inflammatory Drugs Jorieke Konijnenbelt‐Peters, Charlotte van der Heijden, Corine Ekhart et al. · Pain Practice 27 Jun 2016 99
37 The Quality of Clinical Information in Adverse Drug Reaction Reports by Patients and Healthcare Professionals: A Retrospective Comparative Analysis Leàn Rolfes, Florence P. A. M. van Hunsel, Laura van der Linden et al. · Drug Safety Open access 12 Apr 2017 95
38 Adverse drug reactions of montelukast in children and adults Meindina G. Haarman, Florence P. A. M. van Hunsel, Tjalling W. de Vries · Pharmacology Research & Perspectives Open access 20 Sep 2017 94
39 Hypothermia following antipsychotic drug use Rob J. van Marum, Michelle A. Wegewijs, ANTON J. M. LOONEN et al. · European Journal of Clinical Pharmacology Open access 30 Mar 2007 93
40 Adverse Events Associated With PCSK 9 Inhibitors: A Real‐World Experience Muhammed T. Gürgöze, A H G Muller-Hansma, Michelle M. Schreuder et al. · Clinical Pharmacology & Therapeutics Open access 27 Jul 2018 91
41 Maternal use of SSRIs, SNRIs and NaSSAs: practical recommendations during pregnancy and lactation Sintha D. Sie, JOHANNA M. B. WENNINK, J J van Driel et al. · Archives of Disease in Childhood Fetal & Neonatal 18 Oct 2012 89
42 Comparing patients' and healthcare professionals' ADR reports after media attention: the broadcast of a Dutch television programme about the benefits and risks of statins as an example Florence P. A. M. van Hunsel, Anneke Passier, Kees van Grootheest · British Journal of Clinical Pharmacology Open access 26 Feb 2009 88
43 Progressive multifocal leukoencephalopathy in patients treated with fumaric acid esters: a review of 19 cases Robbert-Jan Gieselbach, A H G Muller-Hansma, Martijn T. Wijburg et al. · Journal of Neurology Open access 23 May 2017 87
44 Drug-associated progressive multifocal leukoencephalopathy: a clinical, radiological, and cerebrospinal fluid analysis of 326 cases Roderick P.P.W.M. Maas, A H G Muller-Hansma, Rianne A.J. Esselink et al. · Journal of Neurology Open access 11 Jul 2016 86
45 Adverse drug reaction reports of patients and healthcare professionals—differences in reported information Leàn Rolfes, Florence P. A. M. van Hunsel, Sarah Wilkes et al. · Pharmacoepidemiology and Drug Safety Open access 31 Jul 2014 86
46 Motives for reporting adverse drug reactions by patient-reporters in the Netherlands Florence P. A. M. van Hunsel, Christine M. Cramer‐van der Welle, Anneke Passier et al. · European Journal of Clinical Pharmacology Open access 23 Jul 2010 85
47 SARS-CoV-2 Vaccine Willingness among Pregnant and Breastfeeding Women during the First Pandemic Wave: A Cross-Sectional Study in Switzerland Sarah Stückelberger, Guillaume Favre, Michael Ceulemans et al. · Viruses Open access 22 Jun 2021 84
48 QT lengthening and life-threatening arrhythmias associated with fexofenadine YM Pinto, IC van Gelder, Marten J. Heeringa et al. · The Lancet Mar 1999 81
49 Surveillance of suspected adverse reactions to natural health products in Italy Francesca Menniti‐Ippolito, Gabriela Mazzanti, Carmela Santuccio et al. · Pharmacoepidemiology and Drug Safety 10 Mar 2008 81
50 Non‐puerperal lactation associated with antidepressant drug use Toine C. G. Egberts, Ronald H.B. Meyboom, Fred H.P. De Koning et al. · British Journal of Clinical Pharmacology Open access Sep 1997 80

Citations are OpenAlex's own counts, from its 2026-09-23 snapshot, so the ranking can differ from Google Scholar or Web of Science. A paper is listed for an institution when any of its authors gave it as an affiliation; retracted papers and papers whose citation count cannot be traced to citing works are left out, and a preprint and the article it became are shown once. Release dates are OpenAlex's: where a source gave only a month or a year, that is what is shown. How the lists are chosen.