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
126411502	12641150	2	F	2015	20160809	20160810	20160811	EXP		PHHY2016BR109399	NOVARTIS		89.68	YR		F	Y	52.00000	KG	20160811		MD	BR	BR

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
126411502	12641150	1	PS	EXELON PATCH	RIVASTIGMINE	1	Transdermal	QD	22083			TRANS-THERAPEUTIC-SYSTEM	QD
126411502	12641150	2	SS	EXELON PATCH	RIVASTIGMINE	1			22083			TRANS-THERAPEUTIC-SYSTEM
126411502	12641150	3	C	NEOTIAPIM	QUETIAPINE	1	Oral	2 DF, QD	0	2	DF	TABLET	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126411502	12641150	1	Oxygen saturation decreased
126411502	12641150	2	Asthenia
126411502	12641150	3	Emotional disorder

Outcome of event

Event ID	CASEID	OUTC COD
126411502	12641150	DE

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
126411502	12641150		Cardiac arrest
126411502	12641150		Product use issue

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
126411502	12641150	1	2015		0
126411502	12641150	3	201603		0