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
126655962	12665596	2	F	2016	20160919	20160818	20160920	PER		US-SHIRE-US201610484	SHIRE		8.78	YR			Y	0.00000		20160920		PH	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	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
126655962	12665596	1	PS	VYVANSE	LISDEXAMFETAMINE DIMESYLATE	1	Oral	40 MG, UNKNOWN	2900	MG	21977	40	MG	CAPSULE
126655962	12665596	2	SS	VYVANSE	LISDEXAMFETAMINE DIMESYLATE	1	Oral	UNK	2900	MG	21977			CAPSULE
126655962	12665596	3	SS	VYVANSE	LISDEXAMFETAMINE DIMESYLATE	1	Oral	50 MG, 1X/DAY:QD	2900	MG	21977	50	MG	CAPSULE	QD
126655962	12665596	4	SS	VYVANSE	LISDEXAMFETAMINE DIMESYLATE	1	Oral	40 MG, UNKNOWN	2900	MG	21977	40	MG	CAPSULE

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126655962	12665596	1	Product used for unknown indication

Outcome of event

no results found

no results found

Reactions reported

Event ID	CASEID	PT
126655962	12665596	Adverse event
126655962	12665596	Product quality issue
126655962	12665596	Underdose
126655962	12665596	Unevaluable event
126655962	12665596	Wrong technique in product usage process

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
126655962	12665596	1		20160614
126655962	12665596	3	20160614	20160811
126655962	12665596	4	20160811