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Prospective data mining of six products in the US FDA Adverse Event Reporting System: disposition of events identified and impact on product safety profiles.
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FAERS
2010/1/20
Priapism associated with antipsychotics: role of alpha1 adrenoceptor affinity.
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FAERS
2010/01/16
Sudden sensorineural hearing loss associated with vardenafil.
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FAERS
2009/12/25
Topical bovine thrombin: a 21-year review of topical bovine thrombin spontaneous case safety reports submitted to FDA’s Adverse Event Reporting System.
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FAERS
2009/12/17
Safety of influenza A (H1N1) 2009 monovalent vaccines – United States, October 1-November 24, 2009.
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VAERS
2009/12/17
Clinical trial and post-licensure safety profile of a prophylactic human papillomavirus (types 6, 11, 16, and 18) l1 virus-like particle vaccine.
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VAERS
2009/12/3
Prediction of drug-related cardiac adverse effects in humans–A: creation of a database of effects and identification of factors affecting their occurrence.
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FAERS
2009/11/26
Omalizumab-associated anaphylactic reactions reported between January 2007 and June 2008.
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FAERS
2009/11/26
Fragment-based prediction of the clinical occurrence of long QT syndrome and torsade de pointes.
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FAERS
2009/11/10
Kawasaki disease after vaccination: reports to the vaccine adverse event reporting system 1990-2007.
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VAERS
2009/09/17
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