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Robin E Ferner

Showing results (51-60 of 100) with videos related to

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Drug Safety|August 16, 2017
Deaths from Medicines: A Systematic Analysis of Coroners' Reports to Prevent Future DeathsRobin E Ferner, Craig Easton, Anthony R Cox
British Journal of Clinical Pharmacology|July 17, 2023
Drug shortages. Part 1. Definitions and harmsJeffrey K Aronson, Carl Heneghan, Robin E Ferner
Drug Safety|November 18, 2009
Improving follow-up rates in spontaneous adverse drug reaction reporting: effectiveness of a targeted letter used by a regional centre in the UKChristopher Anton, Anthony R Cox, Robin E Ferner
Drug Safety|February 17, 2016
Evidence of Misclassification of Drug-Event Associations Classified as Gold Standard 'Negative Controls' by the Observational Medical Outcomes Partnership (OMOP)Manfred Hauben, Jeffrey K Aronson, Robin E Ferner
BMJ (Clinical Research Ed.)|July 26, 2018
Prescribing biosimilarsJeffrey K Aronson, Ben Goldacre, Robin E Ferner
Drug Safety|February 25, 2009
A strategy for regulatory action when new adverse effects of a licensed product emergeJeffrey K Aronson, Deirdre Price, Robin E Ferner
BMJ Evidence-Based Medicine|December 22, 2021
Deaths attributed to the use of medications purchased onlineJeffrey K Aronson, Robin E Ferner, Georgia C Richards
British Journal of Clinical Pharmacology|July 15, 2009
The pathophysiology of medication errors: how and where they ariseSarah E McDowell, Harriet S Ferner, Robin E Ferner
Drug Safety|June 28, 2012
Dose omissions in hospitalized patients in a UK hospital: an analysis of the relative contribution of adverse drug reactionsJamie J Coleman, Sarah E McDowell, Robin E Ferner
BMJ (Clinical Research Ed.)|January 7, 2010
NICE and new: appraising innovationRobin E Ferner, Dyfrig A Hughes, Jeffrey K Aronson
Pageof 10

Showing results (51-60 of 100) with videos related to

Sort By:
Pageof 10
Drug Safety|August 16, 2017
Deaths from Medicines: A Systematic Analysis of Coroners' Reports to Prevent Future DeathsRobin E Ferner, Craig Easton, Anthony R Cox
British Journal of Clinical Pharmacology|July 17, 2023
Drug shortages. Part 1. Definitions and harmsJeffrey K Aronson, Carl Heneghan, Robin E Ferner
Drug Safety|November 18, 2009
Improving follow-up rates in spontaneous adverse drug reaction reporting: effectiveness of a targeted letter used by a regional centre in the UKChristopher Anton, Anthony R Cox, Robin E Ferner
Drug Safety|February 17, 2016
Evidence of Misclassification of Drug-Event Associations Classified as Gold Standard 'Negative Controls' by the Observational Medical Outcomes Partnership (OMOP)Manfred Hauben, Jeffrey K Aronson, Robin E Ferner
BMJ (Clinical Research Ed.)|July 26, 2018
Prescribing biosimilarsJeffrey K Aronson, Ben Goldacre, Robin E Ferner
Drug Safety|February 25, 2009
A strategy for regulatory action when new adverse effects of a licensed product emergeJeffrey K Aronson, Deirdre Price, Robin E Ferner
BMJ Evidence-Based Medicine|December 22, 2021
Deaths attributed to the use of medications purchased onlineJeffrey K Aronson, Robin E Ferner, Georgia C Richards
British Journal of Clinical Pharmacology|July 15, 2009
The pathophysiology of medication errors: how and where they ariseSarah E McDowell, Harriet S Ferner, Robin E Ferner
Drug Safety|June 28, 2012
Dose omissions in hospitalized patients in a UK hospital: an analysis of the relative contribution of adverse drug reactionsJamie J Coleman, Sarah E McDowell, Robin E Ferner
BMJ (Clinical Research Ed.)|January 7, 2010
NICE and new: appraising innovationRobin E Ferner, Dyfrig A Hughes, Jeffrey K Aronson
Pageof 10