Safety Rates Drug Report: adverse events in 2013 Q1 - FDA prescription drugs adverse events in an open, searchable, online, public database

Drug Injury Quarter

Person who experienced the adverse event (patient)

Event ID	CASEID	CASEVERSION	I F COD	EVENT DT	MFR DT	INIT FDA DT	FDA DT	REPT COD	AUTH NUM	MFR NUM	MFR SNDR	LIT REF	AGE	AGE COD	AGE GRP	GNDR COD	E SUB	WT	WT COD	REPT DT	TO MFR	OCCP COD	REPORTER COUNTRY	OCCR COUNTRY
90600381	9060038	1	I		0	20130207	20130207	DIR					75.00	YR		F	N	162.00000	LBS	20130129		CN	US

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	VAL VBM	DOSE VBM	DECHAL	RECHAL	LOT NUM	EXP DT	DOSE AMT	DOSE UNIT	DOSE FREQ
90600381	9060038	1	PS	ZOLIPIDERM TARTRATE 10MG (TORRENT)	1	10 MG 1 AT BEDTIME	N	D	BM691078	20130731	10	MG	X1QHS
90600381	9060038	2	SS	ZOLPEDEM TARTRATE 10MG (TORRENT)	1	10 MG 1 AT BEDTIME	Y	D	BM692003	20141231	10	MG	X1QHS
90600381	9060038	3	SS	ZOLPIDEM TARTRATE 10 MG (TORRENT)	1	10 MG 1 AT BEDTIME	Y	D	BM692004	20150131	10	MG	X1@HS

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
90600381	9060038	1	Sleep disorder
90600381	9060038	2	Sleep disorder
90600381	9060038	3	Sleep disorder

Outcome of event

Event ID	CASEID	OUTC COD
90600381	9060038	OT

Reactions reported

Event ID	CASEID	PT
90600381	9060038	Disorientation
90600381	9060038	Feeling abnormal
90600381	9060038	Hypoaesthesia
90600381	9060038	Neck pain
90600381	9060038	Pain in extremity

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID	CASEID	RPSR COD
90600381	9060038	CSM

Therapies reported

Event ID	CASEID	DSG DRUG SEQ	START DT	END DT
90600381	9060038	1	20120503	20121015
90600381	9060038	2	20121015
90600381	9060038	3		20121015