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A Disproportionality Analysis of the Adverse Drug Events Associated with Lurasidone in Paediatric Patients Using the US FDA Adverse Event Reporting System (FAERS)
Drug Safety
◽
10.1007/s40264-020-00928-1
◽
2020
◽
Vol 43
(6)
◽
pp. 607-609
Author(s):
Kate E. Rees
◽
Te-yuan Chyou
◽
Prasad S. Nishtala
Keyword(s):
Adverse Event
◽
Adverse Drug Events
◽
Reporting System
◽
Adverse Event Reporting System
◽
Adverse Event Reporting
◽
Disproportionality Analysis
◽
Event Reporting
◽
Paediatric Patients
◽
The Us
◽
Us Fda
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Analysis of the US FDA adverse event reporting system to identify adverse cardiac events associated with hydroxychloroquine in older adults
Pharmacoepidemiology and Drug Safety
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10.1002/pds.5155
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2020
◽
Vol 29
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pp. 1689-1695
Author(s):
Prasad S. Nishtala
◽
Sakirat Gill
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Keyword(s):
Older Adults
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Reporting System
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Event Reporting
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SGLT2 inhibitors and amputations in the US FDA Adverse Event Reporting System
The Lancet Diabetes & Endocrinology
◽
10.1016/s2213-8587(17)30257-7
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2017
◽
Vol 5
(9)
◽
pp. 680-681
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Cited By ~ 82
Author(s):
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Keyword(s):
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Adverse Event Reporting
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ATYPICAL ANTIPSYCHOTIC DRUGS AND DIABETES MELLITUS IN THE US FDA ADVERSE EVENT REPORTING SYSTEM (AERS) DATABASE IN PEDIATRIC AND ADULT PATIENTS
Schizophrenia Research
◽
10.1016/s0920-9964(08)70738-2
◽
2008
◽
Vol 102
(1-3)
◽
pp. 245
Author(s):
Estelle Vester-Blokland
◽
Ramin B Arani
◽
David Gan
◽
Andrei Pikalov
◽
Quynh-Van Tran
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...
Keyword(s):
Diabetes Mellitus
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Adverse Event
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Atypical Antipsychotic
◽
Antipsychotic Drugs
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Adverse Event Reporting System
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Adverse Event Reporting
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An Evaluation of Postmarketing Reports with an Outcome of Death in the US FDA Adverse Event Reporting System
Drug Safety
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10.1007/s40264-020-00908-5
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2020
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Vol 43
(5)
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pp. 457-465
◽
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Author(s):
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PCN200 ASSESSMENT OF THE SAFETY OF ONCOLOGY THERAPEUTIC BIOLOGIC DRUGS USING THE US FDA ADVERSE EVENT REPORTING SYSTEM
Value in Health
◽
10.1016/j.jval.2020.04.1675
◽
2020
◽
Vol 23
◽
pp. S57
Author(s):
K. Lotfi
◽
H. Althobaiti
◽
R. Rodriguez-Monguio
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E. Seoane-Vazquez
Keyword(s):
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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Biologic Drugs
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Event Reporting
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The US FDA is posting on its website quarterly reports concerning potential safety issues identified through the agency's Adverse Event Reporting System
Reactions Weekly
◽
10.2165/00128415-200812190-00007
◽
2008
◽
Vol &NA;
(1219)
◽
pp. 4
Author(s):
&NA;
Keyword(s):
Adverse Event
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Adverse Event Reporting System
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Adverse Event Reporting
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Event Reporting
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Potential Safety
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Novel Adverse Events of Bevacizumab in the US FDA Adverse Event Reporting System Database
Drug Safety
◽
10.2165/11597600-000000000-00000
◽
2012
◽
Vol 35
(6)
◽
pp. 507-518
◽
Cited By ~ 25
Author(s):
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◽
Pankdeep Chhabra
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Andrew N. Freedman
◽
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◽
Jennifer Malin
◽
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Keyword(s):
Adverse Event
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Adverse Events
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Reporting System
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Adverse Event Reporting System
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Prospective Data Mining of Six Products in the US FDA Adverse Event Reporting System
Drug Safety
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10.2165/11319000-000000000-00000
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◽
Vol 33
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◽
pp. 139-146
◽
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Author(s):
Steven Bailey
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Ajay Singh
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Robert Azadian
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Peter Huber
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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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Prospective Data
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Event Reporting
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Safety of Marketed Cancer Supportive Care Biosimilars in the US: A Disproportionality Analysis Using the Food and Drug Administration Adverse Event Reporting System (FAERS) Database
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Drug Administration
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Food And Drug Administration
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Adverse Event Reporting
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Disproportionality Analysis
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Systemic quinolones and risk of acute liver failure I: Analysis of data from the US FDA adverse event reporting system
JGH Open
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10.1002/jgh3.12585
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2021
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Author(s):
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Abdallah Alami
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Keyword(s):
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Acute Liver Failure
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Adverse Event Reporting System
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Adverse Event Reporting
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Event Reporting
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Us Fda
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