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
127001201	12700120	1	I		20160819	20160830	20160830	EXP		BR-ELI_LILLY_AND_COMPANY-BR201608010434	ELI LILLY AND CO		0.00			M	Y	0.00000		20160830		CN	BR	BR

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
127001201	12700120	1	PS	CIALIS	TADALAFIL	1	Unknown	20 MG, UNKNOWN			Y	U			21368	20	MG	TABLET
127001201	12700120	2	SS	CIALIS	TADALAFIL	1		20 MG, PRN			Y	U	C583455		21368	20	MG	TABLET

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127001201	12700120	1	Product used for unknown indication

Outcome of event

Event ID	CASEID	OUTC COD
127001201	12700120	OT

Reactions reported

Event ID	CASEID	PT
127001201	12700120	Drug ineffective
127001201	12700120	Haemorrhoids
127001201	12700120	Intentional product misuse
127001201	12700120	Suspected counterfeit product
127001201	12700120	Wrong technique in product usage process

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
127001201	12700120	1	2011		0
127001201	12700120	2	20160710		0