Safety Rates Drug Report: adverse events in 2016 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	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
125839573	12583957	3	F	2007	20160824	20160722	20160829	EXP		PHHY2016AR100149	NOVARTIS		80.00	YR		F	Y	0.00000		20160829		CN	AR	AR

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	CUM DOSE CHR	CUM DOSE UNIT	DECHAL	RECHAL	LOT NUM	EXP DT	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
125839573	12583957	1	SS	SINTROM	ACENOCOUMAROL	1	Unknown	0.5 DF ON MONDAYS AND 0.25 DF THE REST OF THE DAYS							0
125839573	12583957	2	PS	FEMARA	LETROZOLE	1	Unknown				U				20726

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125839573	12583957	1	Coagulopathy
125839573	12583957	2	Breast cancer recurrent

Outcome of event

Event ID	CASEID	OUTC COD
125839573	12583957	DS
125839573	12583957	HO

Reactions reported

Event ID	CASEID	PT
125839573	12583957	Arthritis infective
125839573	12583957	Drug ineffective
125839573	12583957	Motor dysfunction
125839573	12583957	Nosocomial infection
125839573	12583957	Osteoarthritis

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

no results found

no results found

Therapies reported

Event ID	CASEID	DSG DRUG SEQ	START DT	END DT	DUR	DUR COD
125839573	12583957	1	200709		0
125839573	12583957	2	200709		0