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Isla Mackenzie

Showing results (1-10 of 7) with videos related to

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Trials|June 6, 2020
Cluster randomised trials of prescribing policy: an ethical approach to generating drug safety evidence? A discussion of the ethical application of a new research methodAmy Rogers, Gillian Craig, Angela Flynn, et al.
British Journal of Clinical Pharmacology|March 10, 2017
Electronic case report forms and electronic data capture within clinical trials and pharmacoepidemiologyDavid A Rorie, Robert W V Flynn, Kerr Grieve, et al.
BMJ Open|June 1, 2022
Adverse events and overall health and well-being after COVID-19 vaccination: interim results from the VAC4COVID cohort safety studyAmy Rogers, Evelien Rooke, Steve Morant, et al.
Antioxidants (Basel, Switzerland)|August 26, 2022
The Prognostic Value of Derivatives-Reactive Oxygen Metabolites (d-ROMs) for Cardiovascular Disease Events and Mortality: A ReviewFilippo Pigazzani, Davide Gorni, Kenneth A Dyar, et al.
Lancet (London, England)|September 29, 2015
Spironolactone versus placebo, bisoprolol, and doxazosin to determine the optimal treatment for drug-resistant hypertension (PATHWAY-2): a randomised, double-blind, crossover trialBryan Williams, Thomas M MacDonald, Steve Morant, et al.
Pharmacoepidemiology and Drug Safety|January 2, 2021
Impact of EMA regulatory label changes on hydroxyzine initiation, discontinuation and switching to other medicines in Denmark, Scotland, England and the Netherlands: An interrupted time series regression analysisDaniel R Morales, Tatiana Macfarlane, Thomas M MacDonald, et al.
Research Involvement and Engagement|July 7, 2026
Embedding the public voice in clinical trials: developing public-informed training for patient data researchFiona V Lugg-Widger, Caroline Brocklehurst, Sarah Chave, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Trials|June 6, 2020
Cluster randomised trials of prescribing policy: an ethical approach to generating drug safety evidence? A discussion of the ethical application of a new research methodAmy Rogers, Gillian Craig, Angela Flynn, et al.
British Journal of Clinical Pharmacology|March 10, 2017
Electronic case report forms and electronic data capture within clinical trials and pharmacoepidemiologyDavid A Rorie, Robert W V Flynn, Kerr Grieve, et al.
BMJ Open|June 1, 2022
Adverse events and overall health and well-being after COVID-19 vaccination: interim results from the VAC4COVID cohort safety studyAmy Rogers, Evelien Rooke, Steve Morant, et al.
Antioxidants (Basel, Switzerland)|August 26, 2022
The Prognostic Value of Derivatives-Reactive Oxygen Metabolites (d-ROMs) for Cardiovascular Disease Events and Mortality: A ReviewFilippo Pigazzani, Davide Gorni, Kenneth A Dyar, et al.
Lancet (London, England)|September 29, 2015
Spironolactone versus placebo, bisoprolol, and doxazosin to determine the optimal treatment for drug-resistant hypertension (PATHWAY-2): a randomised, double-blind, crossover trialBryan Williams, Thomas M MacDonald, Steve Morant, et al.
Pharmacoepidemiology and Drug Safety|January 2, 2021
Impact of EMA regulatory label changes on hydroxyzine initiation, discontinuation and switching to other medicines in Denmark, Scotland, England and the Netherlands: An interrupted time series regression analysisDaniel R Morales, Tatiana Macfarlane, Thomas M MacDonald, et al.
Research Involvement and Engagement|July 7, 2026
Embedding the public voice in clinical trials: developing public-informed training for patient data researchFiona V Lugg-Widger, Caroline Brocklehurst, Sarah Chave, et al.
Pageof 1