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
126768112	12676811	2	F		20160906	20160823	20160908	PER		US-PFIZER INC-2016394614	PFIZER		68.00	YR		M	Y	0.00000		20160908		CN	US	US

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	DOSE VBM	DECHAL	LOT NUM	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
126768112	12676811	1	PS	VIAGRA	SILDENAFIL CITRATE	1	200 MG, UNK	N		20895	200	MG	FILM-COATED TABLET
126768112	12676811	2	SS	VIAGRA	SILDENAFIL CITRATE	1	100 MG, AND TOOK ANOTHER 100 MG	N		20895	100	MG	FILM-COATED TABLET
126768112	12676811	3	SS	VIAGRA	SILDENAFIL CITRATE	1	100 MG, 2X/DAY	N	8001203	20895	100	MG	FILM-COATED TABLET	BID
126768112	12676811	4	SS	VIAGRA	SILDENAFIL CITRATE	1	100 MG, 1X/DAY	N	A602101	20895	100	MG	FILM-COATED TABLET	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126768112	12676811	1	Erectile dysfunction
126768112	12676811	2	Sexual dysfunction

Outcome of event

no results found

no results found

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
126768112	12676811		Drug ineffective
126768112	12676811		Intentional product use issue

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
126768112	12676811	3	201608	20160829	0
126768112	12676811	4	201606		0