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
126218011	12621801	1	I	20160602	20160726	20160804	20160804	EXP		FR-SA-2016SA138028	AVENTIS		36.00	YR	A	M	Y	0.00000		20160804		OT	FR	FR

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	LOT NUM	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
126218011	12621801	1	PS	ZOLPIDEM	ZOLPIDEMOLPIDEM TARTRATE	1	Oral	UNKNOWN	19908	100	MG	FILM-COATED TABLET	1X
126218011	12621801	2	SS	TERCIAN	CYAMEMAZINE	1	Oral	UNKNOWN	0	350	MG	FILM-COATED TABLET	1X
126218011	12621801	3	SS	XANAX	ALPRAZOLAM	1	Oral	UNKNOWN	0	10	DF	TABLET	1X

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126218011	12621801	1	Suicide attempt
126218011	12621801	2	Suicide attempt
126218011	12621801	3	Suicide attempt

Outcome of event

Event ID	CASEID	OUTC COD
126218011	12621801	HO

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
126218011	12621801		Toxicity to various agents

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
126218011	12621801	1	20160602	20160602
126218011	12621801	2	20160602	20160602
126218011	12621801	3	20160602	20160602