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
124664772	12466477	2	F	201606	20160706	20160615	20160714	PER		US-ALEXION-A201604281	ALEXION		0.00			F	Y	0.00000		20160714		CN	US	US

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
124664772	12466477	1	PS	SOLIRIS	ECULIZUMAB	1	Intravenous (not otherwise specified)	1200 MG, Q2W	33818.1836	MG	N	U			125166	1200	MG	CONCENTRATE FOR SOLUTION FOR INFUSION	QOW
124664772	12466477	2	SS	SOLIRIS	ECULIZUMAB	1	Intravenous (not otherwise specified)	1200 MG, Q2W	33818.1836	MG	N	U			125166	1200	MG	CONCENTRATE FOR SOLUTION FOR INFUSION	QOW

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
124664772	12466477	1	Haemolytic uraemic syndrome

Outcome of event

no results found

no results found

Reactions reported

Event ID	CASEID	PT
124664772	12466477	Blood pressure fluctuation
124664772	12466477	Movement disorder
124664772	12466477	Nausea

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
124664772	12466477	1	20150225	20160328	0
124664772	12466477	2	201606	20160624	0