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
122568567	12256856	7	F	201603	20160822	20160412	20160825	EXP		JP-GLAXOSMITHKLINE-JP2016JPN047152	GLAXOSMITHKLINE		70.00	YR		F	Y	50.00000	KG	20160825		MD	JP	JP

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	CUM DOSE CHR	CUM DOSE UNIT	DECHAL	RECHAL	LOT NUM	EXP DT	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
122568567	12256856	1	PS	VALTREX	VALACYCLOVIR HYDROCHLORIDE	1	Oral	1000 MG, TID			Y				20487	1000	MG	TABLET	TID
122568567	12256856	2	SS	VALTREX	VALACYCLOVIR HYDROCHLORIDE	1	Oral	1000 MG, BID			Y				20487	1000	MG	TABLET	BID

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
122568567	12256856	1	Herpes zoster

Outcome of event

Event ID	CASEID	OUTC COD
122568567	12256856	OT
122568567	12256856	HO

Reactions reported

Event ID	CASEID	PT
122568567	12256856	Decreased appetite
122568567	12256856	Headache
122568567	12256856	Malaise
122568567	12256856	Renal impairment

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	DUR	DUR COD
122568567	12256856	1	20160325	20160325	0
122568567	12256856	2	20160326	20160328	0