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
127409472	12740947	2	F	20160614	20160916	20160914	20160915	EXP		CN-009507513-1609CHN005003	MERCK		54.14	YR		M	Y	54.00000	KG	20160915		OT	CN	CN

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	DECHAL	LOT NUM	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
127409472	12740947	1	PS	HYZAAR	HYDROCHLOROTHIAZIDELOSARTAN POTASSIUM	1	Oral	62.5 MG, QD	Y	L034468	20387			TABLET	QD
127409472	12740947	2	C	SHI HUI DA	LEVAMLODIPINE BESYLATE	1	Oral	2.5 MG, QD		160313-2	0	2.5	MG	TABLET	QD
127409472	12740947	3	C	URAPIDIL	URAPIDIL	1	Oral	30 MG, QD		1506331	0	30	MG	SUSTAINED RELEASE TABLET	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127409472	12740947	1	Hypertension
127409472	12740947	2	Hypertension
127409472	12740947	3	Hypertension

Outcome of event

Event ID	CASEID	OUTC COD
127409472	12740947	OT

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
127409472	12740947		Blood uric acid increased

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
127409472	12740947	1	20150601	20150616
127409472	12740947	2	20150601	20150613
127409472	12740947	3	20150601	20150613