Safety Rates Drug Report: SEREVENT DISKUS Device use error adverse events in 2016 Q3 - FDA prescription drugs adverse events in an open, searchable, online, public database

The Safety Rates Drug Report

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Drug Injury Quarter

Drug: SEREVENT DISKUS Injury: Device use error Quarter: 2016Q3

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Total Records: 8 Number of Pages: 1

Event ID	DRUGNAME	PT	Drug Manufacturer	Patient Age	Sex	Weight	Date (YYYYMMDD)	Country
126408831	SEREVENT DISKUS	Device use error	GLAXOSMITHKLINE	0.00	F	0	20160810	US
126520841	SEREVENT DISKUS	Device use error	GLAXOSMITHKLINE	75.81 YR	F	0	20160815	US
126520871	SEREVENT DISKUS	Device use error	GLAXOSMITHKLINE	0.00	F	0	20160815	US
126521942	SEREVENT DISKUS	Device use error	GLAXOSMITHKLINE	0.00	F	0	20160901	US
126989622	SEREVENT DISKUS	Device use error	GLAXOSMITHKLINE	0.00	F	0	20160909	US
127186821	SEREVENT DISKUS	Device use error	GLAXOSMITHKLINE	0.00	M	0	20160906	US
127693731	SEREVENT DISKUS	Device use error	GLAXOSMITHKLINE	81.88 YR	M	0	20160921	US
127876241	SEREVENT DISKUS	Device use error	GLAXOSMITHKLINE	76.15 YR	F	0	20160928	US

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Total Records: 8 Number of Pages: 1

Execution Time: 0.012349843978882 seconds (ucode:4999244). Developed by: James D. Barger