Safety Rates Drug Report: adverse events in 2010 Q2 - 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
6816940	7476623	I		6816940-X	20100327	20100617	20100630	EXP	TPG2010A00398	TAKEDA PHARMACEUTICALS NORTH AMERICA.	76	YR	M	N			20100628					SWITZERLAND

Drug(s) used by person

Event ID	DRUG SEQ	ROLE COD	DRUGNAME	VAL VBM	ROUTE	DOSE VBM	DECHAL	RECHAL	NDA NUM
6816940	1014034917	PS	ACTOS	1	ORAL	45 MG (45 MG, 1 IN 1 D), PER ORAL	Y	D	21073
6816940	1014089817	SS	LANTUS	1	SUBCUTANEOUS	10 IU SUBCUTANEOUS
6816940	1014089823	SS	AMARYL	1	ORAL	4 MG (4 MG, 1 IN 1 D) PER ORAL
6816940	1014089833	SS	GLUCOPHAGE	1	ORAL	1000 MG (1000 MG, 1 IN 1 D) PER ORAL
6816940	1014089836	C	ASPIRIN	1
6816940	1014089837	C	TOLTERODINE TARTRATE	1
6816940	1014089839	C	PRAVASTATIN	1

Indications of drugs used

Event ID	DRUG SEQ	INDI PT
6816940	1014034917	DIABETES MELLITUS
6816940	1014089817	DIABETES MELLITUS

Outcome of event

Event ID	OUTC COD
6816940	HO

Reactions reported

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

Event ID	RPSR COD
6816940	HP
6816940	OTH

Therapies reported

Event ID	DRUG SEQ	END DT
6816940	1014034917	20100327
6816940	1014089817	20100327
6816940	1014089823	20100327
6816940	1014089833	20100327