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
127049991	12704999	1	I	20160829	0	20160831	20160831	DIR					45.00	YR		F	N	71.10000	KG	20160830	N	PH	US

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DECHAL	RECHAL	DOSE AMT	DOSE UNIT	DOSE FREQ
127049991	12704999	1	PS	HYDROXYZINE	HYDROXYZINEHYDROXYZINE HYDROCHLORIDE	1	Oral	D	D	25	MG	PRN
127049991	12704999	2	SS	SOTALOL.	SOTALOL	1	Oral	D	D	80	MG	BID
127049991	12704999	4	C	ZYRTEC	CETIRIZINE HYDROCHLORIDE	1

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127049991	12704999	1	Urticaria
127049991	12704999	2	Ventricular tachycardia

Outcome of event

Reactions reported

Event ID	CASEID	PT
127049991	12704999	Cardiac arrest
127049991	12704999	Torsade de pointes
127049991	12704999	Ventricular fibrillation

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID	CASEID	RPSR COD
127049991	12704999	HP

Therapies reported

Event ID	CASEID	DSG DRUG SEQ	START DT	END DT	DUR	DUR COD
127049991	12704999	2	20151007	20160829	0