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
119205113	11920511	3	F		20160826	20160115	20160831	EXP		CA-ABBVIE-16K-028-1536903-00	ABBVIE		0.00			F	Y	0.00000		20160831		CN	COUNTRY NOT SPECIFIED	CA

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
119205113	11920511	1	PS	HUMIRA	ADALIMUMAB	1	Subcutaneous				U		UNKNOWN		125057	40	MG	SOLUTION FOR INJECTION IN PRE-FILLED PEN	/wk
119205113	11920511	2	SS	HUMIRA	ADALIMUMAB	1	Subcutaneous				U		UNKNOWN		125057	160	MG	SOLUTION FOR INJECTION IN PRE-FILLED PEN

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
119205113	11920511	1	Crohn's disease

Outcome of event

Reactions reported

Event ID	CASEID	PT
119205113	11920511	Amnesia
119205113	11920511	Fall
119205113	11920511	Gastrointestinal ischaemia
119205113	11920511	Hip fracture
119205113	11920511	Limb injury
119205113	11920511	Malaise
119205113	11920511	Muscle atrophy

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
119205113	11920511	1	20120531	2015	0
119205113	11920511	2	20160527	20160527	0