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1

Do pharmacists' reports of adverse drug reactions reflect patients' concerns?

Kees van Grootheest, Eugène P. van Puijenbroek, Lolkje T.W. de Jong-van den Berg

Journal:

International Journal of Clinical Pharmacy

Year:

2004

Language:

english

File:

PDF, 62 KB

english, 2004

2

Pharmacists' role in reporting adverse drug reactions in an international perspective

Kees van Grootheest, Sten Olsson, Mary Couper, Lolkje de Jong-van den Berg

Journal:

Pharmacoepidemiology and Drug Safety

Year:

2004

Language:

english

File:

PDF, 85 KB

english, 2004

3

Consumer Adverse Drug Reaction Reporting

Dr Kees van Grootheest, Linda de Graaf, Lolkje T.W. de Jong-van den Berg

Journal:

Year:

2003

Language:

english

File:

PDF, 87 KB

english, 2003

4

Spontaneous ADR Reports as a Trigger for Pharmacogenetic Research

Dr Eugène van Puijenbroek, Jean Conemans, Kees van Grootheest

Journal:

Year:

2009

Language:

english

File:

PDF, 195 KB

english, 2009

5

Determinants of signal selection in a spontaneous reporting system for adverse drug reactions

Eugène P. Van Puijenbroek, Kees Van Grootheest, Willem L Diemont, Hubert G. M. Leufkens, Antoine C. G. Egberts

Journal:

British Journal of Clinical Pharmacology

Year:

2001

Language:

english

File:

PDF, 81 KB

english, 2001

6

Expectations of general practitioners and specialist doctors regarding the feedback received after reporting an adverse drug reaction

Lotte Cornelissen, Eugène van Puijenbroek, Kees van Grootheest

Journal:

Pharmacoepidemiology and Drug Safety

Year:

2008

Language:

english

File:

PDF, 228 KB

english, 2008

7

Media attention and the influence on the reporting odds ratio in disproportionality analysis: an example of patient reporting of statins

Florence van Hunsel, Eugène van Puijenbroek, Lolkje de Jong- van den Berg, Kees van Grootheest

Journal:

Pharmacoepidemiology and Drug Safety

Year:

2010

Language:

english

File:

PDF, 131 KB

english, 2010

8

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, Lolkje de Jong-van den Berg, Kees van Grootheest

Journal:

Pharmacoepidemiology and Drug Safety

Year:

2011

Language:

english

File:

PDF, 111 KB

english, 2011

9

Longitudinal monitoring of the safety of drugs by using a web-based system: the case of pregabalin

Linda Härmark, Eugene van Puijenbroek, Kees van Grootheest

Journal:

Pharmacoepidemiology and Drug Safety

Year:

2011

Language:

english

File:

PDF, 241 KB

english, 2011

10

Mirena® en uterusperforatie

Mark de Groot, Kees van Grootheest

Journal:

Huisarts en wetenschap

Year:

2005

Language:

dutch

File:

PDF, 66 KB

dutch, 2005

11

Motives for reporting adverse drug reactions by patient-reporters in the Netherlands

Florence van Hunsel, Christine van der Welle, Anneke Passier, Eugène van Puijenbroek, Kees van Grootheest

Journal:

European Journal of Clinical Pharmacology

Year:

2010

Language:

english

File:

PDF, 160 KB

english, 2010

12

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

Journal:

British Journal of Clinical Pharmacology

Year:

2009

Language:

english

File:

PDF, 552 KB

english, 2009

13

Neuropsychiatric symptoms during cefepime treatment

Willem Diemont, Marius MacKenzie, Nicolaas Sxhaap, Gerard Goverde, Hedwig van Heereveld, Yechiel Hekster, Kees van Grootheest

Journal:

International Journal of Clinical Pharmacy

Year:

2001

Language:

english

File:

PDF, 98 KB

english, 2001

14

Epistaxis and other haemorrhagic events associated with the smoking cessation medicine varenicline: a case series from two national pharmacovigilance centres

Harrison-Woolrych, Mira, Härmark, Linda, Tan, Ming, Maggo, Simran, Grootheest, Kees

Journal:

European Journal of Clinical Pharmacology

Year:

2012

Language:

english

File:

PDF, 155 KB

english, 2012

15

Patients' motives for participating in active post-marketing surveillance

Linda Härmark, Miguel Lie-Kwie, Lisette Berm, Han de Gier, Kees van Grootheest

Journal:

Pharmacoepidemiology and Drug Safety

Year:

2012

Language:

english

File:

PDF, 134 KB

english, 2012

16

Representativeness of diabetes patients participating in a web-based adverse drug reaction monitoring system

Linda Härmark, Susanne Alberts, Eugène van Puijenbroek, Petra Denig, Kees van Grootheest

Journal:

Pharmacoepidemiology and Drug Safety

Year:

2012

Language:

english

File:

PDF, 139 KB

english, 2012

17

Monitoring the safety of influenza A (H1N1) vaccine using web-based intensive monitoring

Linda Härmark, Florence van Hunsel, Eelko Hak, Kees van Grootheest

Journal:

Year:

2011

Language:

english

File:

PDF, 285 KB

english, 2011

18

Labelling and ‘Dear Doctor’ Letters

Dr A.C. Kees van Grootheest, I. Ralph Edwards

Journal:

Year:

2002

Language:

english

File:

PDF, 70 KB

english, 2002

19

Application of Quantitative Signal Detection in the Dutch Spontaneous Reporting System for Adverse Drug Reactions

Dr Eugène P. van Puijenbroek, Willem L. Diemont, Kees van Grootheest

Journal:

Year:

2003

Language:

english

File:

PDF, 113 KB

english, 2003

20

Adverse Drug Reaction-Related Hospitalisations

Cornelis S. van der Hooft, Miriam C.J.M. Sturkenboom, Kees van Grootheest, Herre J. Kingma, Dr Bruno H.Ch. Stricker

Journal:

Year:

2006

Language:

english

File:

PDF, 101 KB

english, 2006

21

Adverse Drug Reaction Reporting by Patients in the Netherlands Three Years of Experience

de Langen, Joyce, van Hunsel, Florence, Passier, Anneke, de Jong-van den Berg, Lolkje, van Grootheest, Kees

Journal:

Year:

2008

Language:

english

File:

PDF, 109 KB

english, 2008

22

Spontaneous Reports and Pharmacogenetics

Eugène van Puijenbroek, Jean Conemans, Kees van Grootheest

Journal:

Year:

2009

Language:

english

File:

PDF, 67 KB

english, 2009

23

Reporting of Adverse Drug Reactions by General Practitioners

Anneke Passier PhD, Marije ten Napel, Kees van Grootheest, Eugène van Puijenbroek

Journal:

Year:

2009

Language:

english

File:

PDF, 185 KB

english, 2009

24

Fever Following Immunization with Influenza A (H1N1) Vaccine in Children

Nancy Broos MSc, Eugène P. van Puijenbroek, Kees van Grootheest

Journal:

Year:

2010

Language:

english

File:

PDF, 130 KB

english, 2010

25

Uterine Perforation with the Levonorgestrel-Releasing Intrauterine Device

Professor Kees van Grootheest, Bernhardt Sachs, Mira Harrison-Woolrych, Pia Caduff-Janosa, Eugène van Puijenbroek

Journal:

Year:

2011

Language:

english

File:

PDF, 113 KB

english, 2011

26

Monitoring Adverse Events of the Vaccination Campaign Against Influenza A (H1N1) in the Netherlands

Dr Eugène P. van Puijenbroek, Kees van Grootheest

Journal:

Year:

2010

Language:

english

File:

PDF, 168 KB

english, 2010

27

Intensive Monitoring of Pregabalin

Linda Härmark, Eugène van Puijenbroek, Sabine Straus, Kees van Grootheest

Journal:

Year:

2011

Language:

english

File:

PDF, 144 KB

english, 2011

28

Experiences with Adverse Drug Reaction Reporting by Patients

Florence van Hunsel, Linda Härmark, Shanthi Pal, Sten Olsson, Kees van Grootheest

Journal:

Year:

2012

Language:

english

File:

PDF, 180 KB

english, 2012

29

Effectiveness of Pharmacovigilance Training of General Practitioners

Roald Gerritsen, Hans Faddegon, Fred Dijkers, Kees van Grootheest, Eugène van Puijenbroek

Journal:

Year:

2011

Language:

english

File:

PDF, 117 KB

english, 2011

30

The Dawn of Pharmacovigilance

Dr Kees van Grootheest

Journal:

Pharmaceutical Medicine

Year:

2003

Language:

english

File:

PDF, 102 KB

english, 2003

31

Important information regarding reporting of adverse drug reactions: a qualitative study

Rolfes, Leàn, Wilkes, Sarah, van Hunsel, Florence, van Puijenbroek, Eugène, van Grootheest, Kees

Journal:

International Journal of Pharmacy Practice

Year:

2014

Language:

english

File:

PDF, 185 KB

english, 2014

32

Non-response in a pharmacy and patient-based intensive monitoring system: a quantitative study on non-response bias and reasons for non-response

Härmark, Linda V.D., Huls, Harmen J., de Gier, J.J. Han, van Grootheest, A.C. Kees

Journal:

International Journal of Pharmacy Practice

Year:

2014

Language:

english

File:

PDF, 220 KB

english, 2014

33

Patients’ role in reporting adverse drug reactions

van Grootheest, Kees, de Jong-van den Berg, Lolkje

Journal:

Expert Opinion on Drug Safety

Year:

2004

Language:

english

File:

PDF, 94 KB

english, 2004

34

Feedback for patients reporting adverse drug reactions; satisfaction and expectations

Rolfes, Leàn, van Hunsel, Florence, van Grootheest, Kees, van Puijenbroek, Eugène

Journal:

Expert Opinion on Drug Safety

Year:

2015

Language:

english

File:

PDF, 382 KB

english, 2015

35

Web-based intensive monitoring: from passive to active drug surveillance

Härmark, Linda, van Grootheest, Kees

Journal:

Expert Opinion on Drug Safety

Year:

2012

Language:

english

File:

PDF, 213 KB

english, 2012

36

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

Rolfes, Leàn, van Hunsel, Florence, Wilkes, Sarah, van Grootheest, Kees, van Puijenbroek, Eugène

Journal:

Pharmacoepidemiology and Drug Safety

Year:

2015

Language:

english

File:

PDF, 204 KB

english, 2015

37

Adjuvanted A/H1N1 (2009) influenza vaccination during pregnancy: Description of a prospective cohort and spontaneously reported pregnancy-related adverse reactions in the Netherlands

de Vries, Loes, van Hunsel, Florence, Cuppers-Maarschalkerweerd, Benedikte, van Puijenbroek, Eugène, van Grootheest, Kees

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2014

Language:

english

File:

PDF, 87 KB

english, 2014