Safety Rates Drug Report: adverse events in 2008 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
5714323	6634392	I		5714323-7	20080411	20080417	20080421	EXP	2008SP007228	SCHERING-PLOUGH CORPORATION	68	YR	M	N	67	KG	20080418	MD	20080411			GERMANY

Drug(s) used by person

Event ID	DRUG SEQ	ROLE COD	DRUGNAME	VAL VBM	ROUTE	DOSE VBM	DECHAL	RECHAL	NDA NUM
5714323	1009821516	PS	TEMOZOLOMIDE	1	ORAL	75MG/M2; PO; 200 MG/M2; QD; PO	D	D	21029
5714323	1009880570	SS	DIPYRONE TAB	1		20 GTT;PRN	D	D
5714323	1009880572	SS	HYDROCHLOROTHIAZIDE	2	ORAL	25 MG; QD; PO	D	D
5714323	1009880573	SS	TORSEMIDE	1	ORAL	10 MG; BID; PO; 10 MG; QD; PO	D	D
5714323	1009880577	SS	BISOPROLOL FUMARATE	1		2.5 MG; QD;	D	D
5714323	1009880579	SS	LISINOPRIL	1	ORAL	20 MG; QD ; PO	D	D
5714323	1009880600	SS	DEXAMETHASONE	1	ORAL	2 MG; TID; PO; 2 MG; QD; PO	D	D
5714323	1009880601	SS	NEXIUM	1	ORAL	40 MG; QD; PO	D	D
5714323	1009880603	C	FELODIPINE	1

Indications of drugs used

Outcome of event

Event ID	OUTC COD
5714323	DE
5714323	HO

Reactions reported

Event ID	PT
5714323	CARDIAC DISORDER
5714323	DYSPNOEA EXERTIONAL
5714323	RED BLOOD CELL COUNT DECREASED
5714323	VENOUS INSUFFICIENCY

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

Therapies reported

Event ID	DRUG SEQ	START DT	END DT
5714323	1009821516	20080327	20080331
5714323	1009821516	20071126
5714323	1009880573	20071211