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
126370781	12637078	1	I	2011	20160726	20160809	20160809	EXP		US-ACORDA-ACO_126778_2016	ACORDA		0.00			M	Y	0.00000		20160809		CN	US	US

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	DECHAL	RECHAL	LOT NUM	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
126370781	12637078	1	PS	AMPYRA	DALFAMPRIDINE	1	Oral	10 BID	Y	U		22250	10	MG	TABLET	BID
126370781	12637078	2	SS	AMPYRA	DALFAMPRIDINE	1	Oral	10 MG, BID	Y	U	0000078437	22250	10	MG	TABLET	BID
126370781	12637078	3	C	ASPIRIN.	ASPIRIN	1	Oral	81 MG, QD				0	81	MG		QD
126370781	12637078	4	C	LASIX	FUROSEMIDE	1	Oral	40 MG, QD				0	40	MG		QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126370781	12637078	1	Nystagmus
126370781	12637078	3	Product used for unknown indication
126370781	12637078	4	Cardiac failure congestive

Outcome of event

Event ID	CASEID	OUTC COD
126370781	12637078	OT

Reactions reported

Event ID	CASEID	PT
126370781	12637078	Delusion
126370781	12637078	Drug ineffective for unapproved indication
126370781	12637078	Insomnia
126370781	12637078	Off label use

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
126370781	12637078	1	2011	2011	0
126370781	12637078	2	20160608	20160615	0