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
125227872	12522787	2	F	201604	20160728	20160701	20160803	EXP		AR-ABBVIE-16P-007-1666475-00	ABBVIE		78.89	YR		M	Y	0.00000		20160803		CN	COUNTRY NOT SPECIFIED	AR

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
125227872	12522787	1	PS	ZEMPLAR	PARICALCITOL	1	Intravenous (not otherwise specified)						UNKNOWN		20819	5	UG	INJECTION	TIW
125227872	12522787	2	C	ENSURE	AMINO ACIDSDEXTROSEELECTROLYTES NOSSOYBEAN OILVITAMINS	1	Oral								0				QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125227872	12522787	1	Hyperparathyroidism secondary
125227872	12522787	2	Decreased appetite

Outcome of event

Reactions reported

Event ID	CASEID	PT
125227872	12522787	Acute respiratory failure
125227872	12522787	Anaemia
125227872	12522787	Cardio-respiratory arrest
125227872	12522787	Decreased appetite
125227872	12522787	Multiple organ dysfunction syndrome
125227872	12522787	Pneumonitis

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
125227872	12522787	1	20151221		0