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
126594191	12659419	1	I	201608	20160808	20160817	20160817	EXP		KR-BAXTER-2016BAX042218	BAXTER		80.27	YR		M	Y	0.00000		20160817		OT	KR	KR

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
126594191	12659419	1	PS	EXTRANEAL	CALCIUM CHLORIDEICODEXTRINMAGNESIUM CHLORIDESODIUM CHLORIDESODIUM LACTATE	1	Intraperitoneal								21321	2	L	SOLUTION FOR PERITONEAL DIALYSIS	QD
126594191	12659419	2	SS	PHYSIONEAL 2.5%	CALCIUM CHLORIDEDEXTROSEMAGNESIUM CHLORIDESODIUM CHLORIDE SOLUTION	1	Intraperitoneal								0	2	L	SOLUTION FOR PERITONEAL DIALYSIS	TID

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126594191	12659419	1	End stage renal disease
126594191	12659419	2	End stage renal disease

Outcome of event

Event ID	CASEID	OUTC COD
126594191	12659419	DE
126594191	12659419	HO

Reactions reported

Event ID	CASEID	PT
126594191	12659419	Cholelithiasis
126594191	12659419	Myocardial infarction
126594191	12659419	Sepsis

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
126594191	12659419	1	20040930	20160807	0
126594191	12659419	2	20040930	20160807	0