Safety Rates Drug Report: adverse events in 2014 Q4 - 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
100465614	10046561	4	F	2014	20141215	20140326	20141231	EXP		US-000960	NPS		45.59	YR		F	N	138.00000	LBS	20141230	N	OT	US

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
100465614	10046561	1	PS	GATTEX	TEDUGLUTIDEWATER	1	SUBCUTANEOUS	DF			D	D			203441				QD
100465614	10046561	3	C	SOLUTION FOR PARENTERAL NUTRITION		2									0

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
100465614	10046561	1	Short-bowel syndrome

Outcome of event

Event ID	CASEID	OUTC COD
100465614	10046561	HO

Reactions reported

Event ID	CASEID	PT
100465614	10046561	Bowel movement irregularity
100465614	10046561	Dehydration
100465614	10046561	Drug dose omission
100465614	10046561	Haemorrhoids
100465614	10046561	Injection site bruising
100465614	10046561	Malnutrition
100465614	10046561	Weight decreased
100465614	10046561	Weight increased

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

Therapies reported

Event ID	CASEID	DSG DRUG SEQ	START DT	END DT	DUR	DUR COD
100465614	10046561	1	201304	20140315	0
100465614	10046561	1	201403		0