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
125850461	12585046	1	I	201607	20160721	20160723	20160723	EXP		DE-009507513-1607DEU008803	MERCK		0.00			F	Y	0.00000		20160723		CN	DE	DE

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	NDA NUM	DOSE FORM
125850461	12585046	1	PS	NUVARING	ETHINYL ESTRADIOLETONOGESTREL	1	Vaginal	UNK	21187	VAGINAL RING
125850461	12585046	2	SS	NUVARING	ETHINYL ESTRADIOLETONOGESTREL	1	Vaginal	UNK	21187	VAGINAL RING
125850461	12585046	3	SS	NUVARING	ETHINYL ESTRADIOLETONOGESTREL	1	Vaginal	UNK	21187	VAGINAL RING

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125850461	12585046	1	Contraception

Outcome of event

Event ID	CASEID	OUTC COD
125850461	12585046	OT

Reactions reported

Event ID	CASEID	PT
125850461	12585046	Abnormal withdrawal bleeding
125850461	12585046	Colitis ulcerative
125850461	12585046	Incorrect drug administration duration

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
125850461	12585046	1	20160623	20160721	0
125850461	12585046	2	201607		0