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Drug Safety
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October 26, 2018
The Role of European Patient Organizations in Pharmacovigilance
Cristiano Matos, Gerda Weits, Florence van Hunsel
Archives of Disease in Childhood
|
April 20, 2016
Adverse drug reactions of systemic antihistamines in children in the Netherlands
Tjalling W de Vries, Florence van Hunsel
Drug Safety
|
January 29, 2015
ADR Reporting by the General Public: Lessons Learnt from the Dutch and Swedish Systems
Linda Härmark, Florence van Hunsel, Birgitta Grundmark
Pharmacoepidemiology and Drug Safety
|
May 20, 2017
The contribution of direct patient reported ADRs to drug safety signals in the Netherlands from 2010 to 2015
Florence van Hunsel, Susan de Waal, Linda Härmark
Archives of Disease in Childhood
|
February 16, 2020
Psychiatric adverse drug reactions in the paediatric population
Corine Ekhart, Tjalling de Vries, Florence van Hunsel
Regulatory Toxicology and Pharmacology : RTP
|
October 21, 2015
Adverse food-drug interactions
Alie de Boer, Florence van Hunsel, Aalt Bast
British Journal of Clinical Pharmacology
|
June 26, 2009
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
Expert Opinion on Drug Safety
|
November 18, 2021
Persistent sexual dysfunction after SSRI withdrawal: a scoping review and presentation of 86 cases from the Netherlands
Katherine Chinchilla Alfaro, Florence van Hunsel, Corine Ekhart
British Journal of Clinical Pharmacology
|
August 6, 2021
Numbers of spontaneous reports: How to use and interpret?
Agnes Kant, Florence van Hunsel, Eugene van Puijenbroek
Vaccines
|
June 25, 2026
Characteristics of Hypotonic-Hyporesponsive Episodes (HHEs) Following Childhood Vaccination: A 13-Year Analysis of Spontaneous Reports to the Dutch Pharmacovigilance Centre Lareb
Sanne Boetzkes, Leontine van Balveren, Florence van Hunsel
Page
of 10
Search research articles
Search
Showing results (11-20 of 91) with videos related to
Sort By:
Page
of 10
Drug Safety
|
October 26, 2018
The Role of European Patient Organizations in Pharmacovigilance
Cristiano Matos, Gerda Weits, Florence van Hunsel
Archives of Disease in Childhood
|
April 20, 2016
Adverse drug reactions of systemic antihistamines in children in the Netherlands
Tjalling W de Vries, Florence van Hunsel
Drug Safety
|
January 29, 2015
ADR Reporting by the General Public: Lessons Learnt from the Dutch and Swedish Systems
Linda Härmark, Florence van Hunsel, Birgitta Grundmark
Pharmacoepidemiology and Drug Safety
|
May 20, 2017
The contribution of direct patient reported ADRs to drug safety signals in the Netherlands from 2010 to 2015
Florence van Hunsel, Susan de Waal, Linda Härmark
Archives of Disease in Childhood
|
February 16, 2020
Psychiatric adverse drug reactions in the paediatric population
Corine Ekhart, Tjalling de Vries, Florence van Hunsel
Regulatory Toxicology and Pharmacology : RTP
|
October 21, 2015
Adverse food-drug interactions
Alie de Boer, Florence van Hunsel, Aalt Bast
British Journal of Clinical Pharmacology
|
June 26, 2009
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
Expert Opinion on Drug Safety
|
November 18, 2021
Persistent sexual dysfunction after SSRI withdrawal: a scoping review and presentation of 86 cases from the Netherlands
Katherine Chinchilla Alfaro, Florence van Hunsel, Corine Ekhart
British Journal of Clinical Pharmacology
|
August 6, 2021
Numbers of spontaneous reports: How to use and interpret?
Agnes Kant, Florence van Hunsel, Eugene van Puijenbroek
Vaccines
|
June 25, 2026
Characteristics of Hypotonic-Hyporesponsive Episodes (HHEs) Following Childhood Vaccination: A 13-Year Analysis of Spontaneous Reports to the Dutch Pharmacovigilance Centre Lareb
Sanne Boetzkes, Leontine van Balveren, Florence van Hunsel
Page
of 10