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
125636991	12563699	1	I	20160229	20160705	20160716	20160716	EXP		CN-JNJFOC-20160702506	JOHNSON AND JOHNSON		6.00	YR	C	M	Y	23.00000	KG	20160715		OT	CN	CN

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
125636991	12563699	1	PS	MOTRIN	IBUPROFEN	1	Intravenous (not otherwise specified)				Y	N	150910027		20516	12	ML	SUSPENSION	QD
125636991	12563699	2	SS	MOTRIN	IBUPROFEN	1	Intravenous (not otherwise specified)				Y	N	150910027		20516	12	ML	SUSPENSION	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125636991	12563699	1	Pyrexia
125636991	12563699	2	Pneumonia

Outcome of event

Event ID	CASEID	OUTC COD
125636991	12563699	OT

Reactions reported

Event ID	CASEID	PT
125636991	12563699	Asthma
125636991	12563699	Incorrect route of drug administration
125636991	12563699	Off label use
125636991	12563699	Product use issue

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
125636991	12563699	1	20160229	20160229	0
125636991	12563699	2	20160229	20160229	0