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JAMA Internal Medicine
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October 30, 2013
Development times, clinical testing, postmarket follow-up, and safety risks for the new drugs approved by the US food and drug administration: the class of 2008
Thomas J Moore, Curt D Furberg
Seminars in Thrombosis and Hemostasis
|
October 23, 2012
Underreporting of hemorrhagic and thrombotic complications of pharmaceuticals to the U.S. Food and Drug Administration: empirical findings for warfarin, clopidogrel, ticlopidine, and thalidomide from the Southern Network on Adverse Reactions (SONAR)
Thomas J Moore, Charles L Bennett
JAMA Internal Medicine
|
December 13, 2016
Adult Utilization of Psychiatric Drugs and Differences by Sex, Age, and Race
Thomas J Moore, Donald R Mattison
JAMA
|
September 6, 2012
The safety risks of innovation: the FDA's Expedited Drug Development Pathway
Thomas J Moore, Curt D Furberg
Plos One
|
December 24, 2010
Prescription drugs associated with reports of violence towards others
Thomas J Moore, Joseph Glenmullen, Curt D Furberg
The Annals of Pharmacotherapy
|
July 22, 2010
Thoughts and acts of aggression/violence toward others reported in association with varenicline
Thomas J Moore, Joseph Glenmullen, Curt D Furberg
Clinical Trials (London, England)
|
March 30, 2019
Globalization of clinical trials: Variation in estimated regional costs of pivotal trials, 2015-2016
Yao Qiao, G Caleb Alexander, Thomas J Moore
Archives of Internal Medicine
|
January 11, 2012
The FDA and new safety warnings
Thomas J Moore, Sonal Singh, Curt D Furberg
The New England Journal of Medicine
|
December 14, 2017
The Fate of FDA Postapproval Studies
Lisa M Schwartz, Steven Woloshin, Thomas J Moore
Pharmacotherapy
|
October 22, 2025
Developing New Drugs for the COVID-19 Emergency: Anatomy of the U.S. Response
Thomas J Moore, Mariana P Socal, Gerard Anderson
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of 8
Search research articles
Search
Showing results (11-20 of 75) with videos related to
Sort By:
Page
of 8
JAMA Internal Medicine
|
October 30, 2013
Development times, clinical testing, postmarket follow-up, and safety risks for the new drugs approved by the US food and drug administration: the class of 2008
Thomas J Moore, Curt D Furberg
Seminars in Thrombosis and Hemostasis
|
October 23, 2012
Underreporting of hemorrhagic and thrombotic complications of pharmaceuticals to the U.S. Food and Drug Administration: empirical findings for warfarin, clopidogrel, ticlopidine, and thalidomide from the Southern Network on Adverse Reactions (SONAR)
Thomas J Moore, Charles L Bennett
JAMA Internal Medicine
|
December 13, 2016
Adult Utilization of Psychiatric Drugs and Differences by Sex, Age, and Race
Thomas J Moore, Donald R Mattison
JAMA
|
September 6, 2012
The safety risks of innovation: the FDA's Expedited Drug Development Pathway
Thomas J Moore, Curt D Furberg
Plos One
|
December 24, 2010
Prescription drugs associated with reports of violence towards others
Thomas J Moore, Joseph Glenmullen, Curt D Furberg
The Annals of Pharmacotherapy
|
July 22, 2010
Thoughts and acts of aggression/violence toward others reported in association with varenicline
Thomas J Moore, Joseph Glenmullen, Curt D Furberg
Clinical Trials (London, England)
|
March 30, 2019
Globalization of clinical trials: Variation in estimated regional costs of pivotal trials, 2015-2016
Yao Qiao, G Caleb Alexander, Thomas J Moore
Archives of Internal Medicine
|
January 11, 2012
The FDA and new safety warnings
Thomas J Moore, Sonal Singh, Curt D Furberg
The New England Journal of Medicine
|
December 14, 2017
The Fate of FDA Postapproval Studies
Lisa M Schwartz, Steven Woloshin, Thomas J Moore
Pharmacotherapy
|
October 22, 2025
Developing New Drugs for the COVID-19 Emergency: Anatomy of the U.S. Response
Thomas J Moore, Mariana P Socal, Gerard Anderson
Page
of 8