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
126586671	12658667	1	I	20150625	0	20160816	20160816	DIR					78.00	YR		M	N	58.90000	KG	20150916	N	PH	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
126586671	12658667	1	PS	LITHIUM.	LITHIUM	1	Oral				D	D			0	1	DF	COATED TABLET	QD
126586671	12658667	2	SS	LITHIUM.	LITHIUM	1	Oral				D	D			0	1	DF	COATED TABLET	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126586671	12658667	1	Bipolar I disorder

Outcome of event

Reactions reported

Event ID	CASEID	PT
126586671	12658667	Cerebrovascular accident
126586671	12658667	Confusional state
126586671	12658667	Delirium
126586671	12658667	Diabetes insipidus
126586671	12658667	Fall
126586671	12658667	Lethargy

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

Event ID	CASEID	RPSR COD
126586671	12658667	HP

Therapies reported

Event ID	CASEID	DSG DRUG SEQ	START DT	END DT	DUR	DUR COD
126586671	12658667	1	20140417	20150717	0
126586671	12658667	2	20140417	20150717	0