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
125737801	12573780	1	I	20160223	20160411	20160718	20160718	PER		DL2016-0203	DANCO		22.00	YR		F	N	0.00000		20160629	N	OT	US

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DECHAL	RECHAL	LOT NUM	EXP DT	NDA NUM	DOSE AMT	DOSE UNIT
125737801	12573780	1	PS	MIFEPRISTONE TABLETS, 200 MG (DANCO LABS)	MIFEPRISTONE	1	Oral	D	D	13010000134	20180930	20687	200	MG
125737801	12573780	2	SS	MISOPROSTOL TABLETS, 200 MCG	MISOPROSTOL	1	Buccal	D	D			0	800	UG
125737801	12573780	4	C	AZITHROMYCIN ANHYDROUS.	AZITHROMYCIN ANHYDROUS	1						0

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125737801	12573780	1	Abortion induced

Outcome of event

Event ID	CASEID	OUTC COD
125737801	12573780	HO

Reactions reported

Event ID	CASEID	PT
125737801	12573780	Abortion incomplete
125737801	12573780	Anaemia
125737801	12573780	Haemorrhage

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID	CASEID	RPSR COD
125737801	12573780	HP

Therapies reported

Event ID	CASEID	DSG DRUG SEQ	START DT	END DT	DUR	DUR COD
125737801	12573780	1	20160203		0
125737801	12573780	2	20160204		0