Kees van Grootheest - Concepedia

Author

Kees van Grootheest

Netherlands Pharmacovigilance Centre Lareb

Also Known As

Grootheest, Kees Van, K Van Grootheest, K. van Grootheest, Kees Grootheest, Kees Van Grootheest, Kees van Grootheest, van Grootheest, Kees, E. Van Puijenbroek, L. Härmark

Publications

Citations

H-Index

Concepts

All Affiliations

Netherlands Pharmacovigilance Centre Lareb University of Groningen Erasmus University Rotterdam Pharmac Dialyse Centrum Groningen

About

Kees van Grootheest is an author at Netherlands Pharmacovigilance Centre Lareb specializing in medicine, pharmacotherapy, and drug safety.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	14	788
2	Public Health	3	3	95
3	Epidemiology	2	2	58
4	Engineering	1	1	144
5	Social Sciences	1	1	12

Kees van Grootheest

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Adverse Drug Reaction-Related Hospitalisations C Hooft, Miriam Sturkenboom, Kees van Grootheest, Drug Safety Drug SafetyDrug HypersensitivityAdverse EventPatient SafetyPharmacotherapy	2006	187
Adverse Drug Reaction Reporting by Patients in the Netherlands Joyce de Langen, Florence van Hunsel, Anneke Passier, Drug Safety Drug SafetyDrug HypersensitivitySubstance AbusePatient SafetyForensic Toxicology	2008	180
Pharmacists' role in reporting adverse drug reactions in an international perspective Kees van Grootheest, Sten Olsson, Mary Couper, Pharmacoepidemiology and Drug Safety	2003	174
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 Drug SafetyDrug HypersensitivityTherapeutic Drug MonitoringEngineeringAdverse Drug Reactions	2003	144
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 van Hunsel, Anneke Passier, Kees van Grootheest British Journal of Clinical Pharmacology	2009	87
Motives for reporting adverse drug reactions by patient-reporters in the Netherlands Florence van Hunsel, Christine M. Cramer‐van der Welle, Anneke Passier, European Journal of Clinical Pharmacology	2010	82
Adverse drug reaction reports of patients and healthcare professionals—differences in reported information Leàn Rolfes, Florence van Hunsel, Sarah Wilkes, Pharmacoepidemiology and Drug Safety	2014	76
Determinants of signal selection in a spontaneous reporting system for adverse drug reactions Eugène van Puijenbroek, Kees van Grootheest, Willem L. Diemont, British Journal of Clinical Pharmacology	2001	70
The proportion of patient reports of suspected ADRs to signal detection in the Netherlands: case–control study Florence van Hunsel, Attje Talsma, Eugène van Puijenbroek, Pharmacoepidemiology and Drug Safety	2010	53
Thromboembolism associated with the new contraceptive Yasmin Kees van Grootheest, Tom Vrieling BMJ	2003	52

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