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
126423901	12642390	1	I	20160511	20160802	20160810	20160810	EXP		PHHY2016IT108416	SANDOZ		67.58	YR		M	Y	0.00000		20160810		OT	IT	IT

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
126423901	12642390	1	PS	IBUPROFEN.	IBUPROFEN	1	Oral	20 DF, ONCE/SINGLE	70733	20	DF		1X
126423901	12642390	2	SS	QUETIAPINE.	QUETIAPINE	1	Oral	12 DF, ONCE/SINGLE	0	12	DF	TABLET	1X
126423901	12642390	3	SS	FLUVOXAMINE	FLUVOXAMINE	1	Oral	15 DF, ONCE/SINGLE	0	15	DF	TABLET	1X

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126423901	12642390	1	Product used for unknown indication
126423901	12642390	2	Product used for unknown indication
126423901	12642390	3	Product used for unknown indication

Outcome of event

Event ID	CASEID	OUTC COD
126423901	12642390	HO

Reactions reported

Event ID	CASEID	PT
126423901	12642390	Drug abuse
126423901	12642390	Loss of consciousness
126423901	12642390	Sopor

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
126423901	12642390	1	20160511
126423901	12642390	2	20160511
126423901	12642390	3	20160511