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
125463171	12546317	1	I	20160702	20160704	20160711	20160711	EXP		PHHY2016CN092319	NOVARTIS		73.00	YR		M	Y	51.00000	KG	20160711		MD	CN	CN

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
125463171	12546317	1	PS	ACLASTA	ZOLEDRONIC ACID	1	Intravenous drip	UNK							21817			SOLUTION FOR INJECTION
125463171	12546317	2	C	HEPARIN CALCIUM	HEPARIN CALCIUM	1	Subcutaneous	5000 IU, QD	55000	IU	Y				0	5000	IU		QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125463171	12546317	1	Osteoporosis
125463171	12546317	2	Product used for unknown indication

Outcome of event

Event ID	CASEID	OUTC COD
125463171	12546317	HO

Reactions reported

Event ID	CASEID	PT
125463171	12546317	Cerebral infarction
125463171	12546317	Coma
125463171	12546317	Loss of consciousness
125463171	12546317	Pyrexia

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
125463171	12546317	1	20160701		0
125463171	12546317	2	20160622	20160704	0