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
116815862	11681586	2	F	20130823	20151026	20151029	20160819	EXP		US-ROCHE-1386292	ROCHE		78.17	YR		M	Y	77.00000	KG	20160819		MD	US	US

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	DECHAL	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FREQ
116815862	11681586	1	PS	CELLCEPT	MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE	1	Oral	200MG/ML	U	50759	6	ML	BID
116815862	11681586	2	SS	CELLCEPT	MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE	1	Oral		U	50759	1200	MG	BID
116815862	11681586	3	SS	CELLCEPT	MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE	1	Oral	4 PO	U	50759	250	MG	BID
116815862	11681586	4	C	MIDODRINE	MIDODRINE	1	Oral			0	10	MG	TID

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
116815862	11681586	1	Myasthenia gravis
116815862	11681586	4	Orthostatic hypotension

Outcome of event

Event ID	CASEID	OUTC COD
116815862	11681586	OT

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
116815862	11681586		Malaise
116815862	11681586		Parkinson's disease

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
116815862	11681586	2	20060905		0
116815862	11681586	4	20110202		0