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
127500762	12750076	2	F	20160903	20160922	20160916	20160929	EXP		CA-JNJFOC-20160907070	JANSSEN		55.31	YR	A	M	Y	0.00000		20160929		CN	CA	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
127500762	12750076	1	SS	STELARA	USTEKINUMAB	1	Subcutaneous				N	N			0	45	MG	SOLUTION FOR INJECTION
127500762	12750076	2	PS	STELARA	USTEKINUMAB	1	Subcutaneous				N	N			125261	45	MG	SOLUTION FOR INJECTION

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127500762	12750076	1	Psoriasis
127500762	12750076	2	Psoriasis

Outcome of event

Event ID	CASEID	OUTC COD
127500762	12750076	OT

Reactions reported

Event ID	CASEID	PT
127500762	12750076	Lower respiratory tract infection
127500762	12750076	Malaise
127500762	12750076	Nasopharyngitis

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
127500762	12750076	1	20131106		0
127500762	12750076	2	20111128		0