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???Extreme Duplication??? in the US FDA Adverse Events Reporting System Database
Drug Safety
◽
10.2165/00002018-200730060-00009
◽
2007
◽
Vol 30
(6)
◽
pp. 551-554
◽
Cited By ~ 37
Author(s):
Manfred Hauben
◽
Lester Reich
◽
James DeMicco
◽
Katherine Kim
Keyword(s):
Adverse Events
◽
Reporting System
◽
System Database
◽
The Us
◽
Us Fda
Download Full-text
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10.2165/11597600-000000000-00000
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13711 Isotretinoin use in acne is associated with a higher odds of the adverse effect of insomnia: Results from the US FDA Adverse Events Reporting System
Journal of the American Academy of Dermatology
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0917 Finasteride is Associated with a Higher Odds of Obstructive Sleep Apnea (OSA): Results from the US FDA Adverse Events Reporting System (FAERS)
SLEEP
◽
10.1093/sleep/zsy061.916
◽
2018
◽
Vol 41
(suppl_1)
◽
pp. A340-A341
Author(s):
M A Gupta
◽
B Vujcic
◽
A D Sheridan
◽
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Antipsychotics and Torsadogenic Risk: Signals Emerging from the US FDA Adverse Event Reporting System Database
Drug Safety
◽
10.1007/s40264-013-0032-z
◽
2013
◽
Vol 36
(6)
◽
pp. 467-479
◽
Cited By ~ 42
Author(s):
Elisabetta Poluzzi
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An Experimental Investigation of Masking in the US FDA Adverse Event Reporting System Database
Drug Safety
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10.2165/11584390-000000000-00000
◽
2010
◽
Vol 33
(12)
◽
pp. 1117-1133
◽
Cited By ~ 33
Author(s):
Hsin-wei Wang
◽
Alan M. Hochberg
◽
Ronald K. Pearson
◽
Manfred Hauben
Keyword(s):
Experimental Investigation
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Adverse Event
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Reporting System
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Adverse Event Reporting System
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Adverse Event Reporting
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0473 Alendronate is Associated With a Significantly Higher Odds of Obstructive Sleep Apnea (OSA): Results from the US FDA Adverse Events Reporting System (FAERS)
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10.1093/sleep/zsz067.471
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Madhulika A Gupta
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Risk of psychiatric adverse events in hidradenitis suppurativa patients treated with biologics: Results from the US FDA Adverse Event Reporting System (FAERS)
Journal of the American Academy of Dermatology
◽
10.1016/j.jaad.2019.06.1170
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2019
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Data Mining of the US FDA’s Adverse Events Reporting System Database to Evaluate Drug–Drug Interactions Associated with Statin-Induced Rhabdomyolysis
Pharmaceutical Medicine
◽
10.1007/s40290-016-0162-6
◽
2016
◽
Vol 30
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pp. 327-337
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PDG5 COMMONLY REPORTED ADVERSE EVENTS ASSOCIATED WITH ANTICOAGULANTS USING FDA ADVERSE EVENT REPORTING SYSTEM DATABASE 2012-2018
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2019
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Adverse Events Associated With the Use of Sipuleucel-T Reported to the US Food and Drug Administration’s Adverse Event Reporting System, 2010-2017
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