Safety Rates Drug Report: adverse events in 2006 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	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
4959780	6008015	F		4959780-9	20060301	20060308	20060331	EXP	JP-BRISTOL-MYERS SQUIBB COMPANY-13316286	BRISTOL-MYERS SQUIBB COMPANY	89	YR	M	Y			20060331	MD	20060301			JAPAN

Drug(s) used by person

Event ID	DRUG SEQ	ROLE COD	DRUGNAME	VAL VBM	ROUTE	NDA NUM
4959780	1007117888	PS	GATIFLOXACIN	1	ORAL	21061
4959780	1007117889	C	MUCOTRON	2
4959780	1007117890	C	LEFTOSE	2
4959780	1007117891	C	THEO-DUR	1
4959780	1007117892	C	ISOSORBIDE DINITRATE	1
4959780	1007117893	C	PANTOSIN	2
4959780	1007117894	C	MAGNESIUM OXIDE	2
4959780	1007117895	C	ADENOSINE TRIPHOSPHATE DISODIUM	2
4959780	1007117896	C	NICORANDIL	2
4959780	1007117897	C	TICLOPIDINE HCL	1
4959780	1007117898	C	ASPIRIN + DI-ALMINATE	2
4959780	1007117899	C	ZANTAC	1
4959780	1007117900	C	FRANDOL TAPE S	2

Indications of drugs used

Event ID	DRUG SEQ	INDI PT
4959780	1007117888	BRONCHITIS

Outcome of event

Reactions reported

Event ID	PT
4959780	HYPOGLYCAEMIA
4959780	PNEUMONIA

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

no results found

no results found

Therapies reported

Event ID	DRUG SEQ	START DT	END DT	DUR	DUR COD
4959780	1007117888	20060216	20060222	7	DAY