Safety Rates Drug Report: adverse events in 2004 Q3 - FDA prescription drugs adverse events in an open, searchable, online, public database

Drug Injury Quarter

Person who experienced the adverse event (patient)

Event ID	CASE	I F COD	FOLL SEQ	IMAGE	EVENT DT	MFR DT	FDA DT	REPT COD	MFR NUM	MFR SNDR	AGE	AGE COD	GNDR COD	E SUB	WT	WT COD	REPT DT	OCCP COD	DEATH DT	TO MFR	CONFID	REPORTER COUNTRY
4466781	4112376	F	3	4466781-6	20040108	20040914	20040930	EXP	8005682	UCB PHARMA, INC.	47	YR	F	N	50	KG	20040922	OT

Drug(s) used by person

Event ID	DRUG SEQ	ROLE COD	DRUGNAME	VAL VBM	ROUTE	DOSE VBM	DECHAL	RECHAL	NDA NUM
4466781	1005268308	PS	KEPPRA	1	ORAL	1500 MG 2/D PO	N	D	21035
4466781	1005289928	SS	KEPPRA	1	ORAL	1000 MG 2/D PO	N	D
4466781	1005289931	SS	TEMODAR	1	ORAL	NI /D PO	N	D
4466781	1005289933	SS	TEMOZOLOMIDE	2	ORAL	NI /D PO	N	D
4466781	1005289934	SS	TEMOZOLOMIDE	2	ORAL	NI /D PO	N	D
4466781	1005289936	SS	RADIATION THERAPY	2			N	D

Indications of drugs used

Outcome of event

Event ID	OUTC COD
4466781	OT

Reactions reported

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

Event ID	RPSR COD
4466781	HP

Therapies reported

Event ID	DRUG SEQ	START DT	END DT
4466781	1005268308	20031211	20040303
4466781	1005289928	20040304	20040708
4466781	1005289931	20031229	20040114
4466781	1005289933	20040405	20040409
4466781	1005289934	20040601	20040604
4466781	1005289936	20031229	20040215