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
126141611	12614161	1	I	20160602	20160726	20160802	20160802	EXP		FR-PFIZER INC-2016362022	PFIZER		36.00	YR		M	Y	0.00000		20160802		OT	FR	FR

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
126141611	12614161	1	PS	XANAX	ALPRAZOLAM	1	Oral	10 DF OF 0.50 MG, SINGLE	18276	5	MG	TABLET
126141611	12614161	2	SS	ZOLPIDEM	ZOLPIDEMOLPIDEM TARTRATE	1	Oral	10 DF OF 10 MG, SINGLE	0	100	MG
126141611	12614161	3	SS	TERCIAN /00759301/	CYAMEMAZINE	1	Oral	14 DF OF 25 MG, SINGLE	0	350	MG

Indications of drugs used

no results found

no results found

Outcome of event

Event ID	CASEID	OUTC COD
126141611	12614161	HO

Reactions reported

Event ID	CASEID	PT
126141611	12614161	Suicide attempt
126141611	12614161	Tachycardia
126141611	12614161	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
126141611	12614161	1	20160602	20160602
126141611	12614161	2	20160602	20160602
126141611	12614161	3	20160602	20160602