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Florence van Hunsel
Florence van Hunsel
Lead Safety Innovation, Netherlands Pharmacovigilance Centre Lareb
Geverifieerd e-mailadres voor lareb.nl
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Adverse drug reaction reporting by patients in the Netherlands three years of experience
J de Langen, F van Hunsel, A Passier, LJ den Berg, K van Grootheest
Drug Safety 31, 515-524, 2008
2422008
Experiences with adverse drug reaction reporting by patients: an 11-country survey
F van Hunsel, L Härmark, S Pal, S Olsson, K van Grootheest
Drug safety 35, 45-60, 2012
1872012
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 …
F Van Hunsel, A Passier, K Van Grootheest
British journal of clinical pharmacology 67 (5), 558-564, 2009
1212009
Motives for reporting adverse drug reactions by patient-reporters in the Netherlands
F van Hunsel, C van der Welle, A Passier, E van Puijenbroek, ...
European journal of clinical pharmacology 66, 1143-1150, 2010
962010
Acute effects of nicotine on attention and response inhibition
EM Bekker, KBE Böcker, F Van Hunsel, MC Van Den Berg, JL Kenemans
Pharmacology Biochemistry and Behavior 82 (3), 539-548, 2005
902005
Adverse drug reactions of montelukast in children and adults
MG Haarman, F van Hunsel, TW de Vries
Pharmacology research & perspectives 5 (5), e00341, 2017
872017
ADR reporting by the general public: lessons learnt from the Dutch and Swedish systems
L Härmark, F Van Hunsel, B Grundmark
Drug safety 38 (4), 337-347, 2015
862015
Adverse drug reaction reports of patients and healthcare professionals—differences in reported information
L Rolfes, F van Hunsel, S Wilkes, K van Grootheest, E van Puijenbroek
Pharmacoepidemiology and drug safety 24 (2), 152-158, 2015
752015
The quality of clinical information in adverse drug reaction reports by patients and healthcare professionals: a retrospective comparative analysis
L Rolfes, F van Hunsel, L van der Linden, K Taxis, E van Puijenbroek
Drug safety 40, 607-614, 2017
692017
Adverse food–drug interactions
A de Boer, F Van Hunsel, A Bast
Regulatory Toxicology and Pharmacology 73 (3), 859-865, 2015
692015
The impact of experiencing adverse drug reactions on the patient’s quality of life: a retrospective cross-sectional study in the Netherlands
L Rolfes, F van Hunsel, K Taxis, E van Puijenbroek
Drug safety 39, 769-776, 2016
662016
The proportion of patient reports of suspected ADRs to signal detection in the Netherlands: case–control study
F van Hunsel, A Talsma, E van Puijenbroek, L de Jong‐van den Berg, ...
pharmacoepidemiology and drug safety 20 (3), 286-291, 2011
592011
Are consumers ready to take part in the Pharmacovigilance System?—A Portuguese preliminary study concerning ADR reporting
C Matos, F van Hunsel, J Joaquim
European journal of clinical pharmacology 71, 883-890, 2015
512015
Risk of candidiasis associated with interleukin-17 inhibitors: A real-world observational study of multiple independent sources
L Davidson, JMPA van den Reek, M Bruno, F van Hunsel, RMC Herings, ...
The Lancet Regional Health–Europe 13, 2022
472022
Safety concerns reported by patients identified in a collaborative signal detection workshop using VigiBase: results and reflections from Lareb and Uppsala Monitoring Centre
S Watson, RE Chandler, H Taavola, L Härmark, B Grundmark, A Zekarias, ...
Drug safety 41, 203-212, 2018
462018
Patient reporting of adverse drug reactions: an international survey of national competent authorities’ views and needs
C Matos, L Härmark, F van Hunsel
Drug safety 39, 1105-1116, 2016
442016
The contribution of direct patient reported ADRs to drug safety signals in the Netherlands from 2010 to 2015
F van Hunsel, S De Waal, L Härmark
Pharmacoepidemiology and Drug Safety 26 (8), 977-983, 2017
432017
Description of frequencies of reported adverse events following immunization among four different COVID-19 vaccine brands
A Kant, J Jansen, L van Balveren, F van Hunsel
Drug safety 45 (4), 319-331, 2022
422022
Important information regarding reporting of adverse drug reactions: a qualitative study
L Rolfes, S Wilkes, F van Hunsel, E van Puijenbroek, K van Grootheest
International Journal of Pharmacy Practice 22 (3), 231-233, 2014
362014
Monitoring the safety of influenza A (H1N1) vaccine using web-based intensive monitoring
L Härmark, F van Hunsel, E Hak, K van Grootheest
Vaccine 29 (10), 1941-1947, 2011
322011
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