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
125698811	12569881	1	I	20160122	20160714	20160719	20160719	EXP	HR-HALMED-2016-01778	HR-GLAXOSMITHKLINE-HR2016101020	GLAXOSMITHKLINE		18.00	YR		F	Y	0.00000		20160719		MD	HR	HR

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
125698811	12569881	1	PS	LAMICTAL	LAMOTRIGINE	1	Oral	12 DF, UNK	20241	12	DF	TABLET
125698811	12569881	2	SS	RIVOTRIL	CLONAZEPAM	1	Oral	25 MG, UNK	0	25	MG	TABLET
125698811	12569881	3	SS	ZALASTA	OLANZAPINE	1	Oral	15 DF, UNK	0	15	DF	TABLET

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125698811	12569881	1	Product used for unknown indication
125698811	12569881	2	Product used for unknown indication
125698811	12569881	3	Product used for unknown indication

Outcome of event

Event ID	CASEID	OUTC COD
125698811	12569881	OT

Reactions reported

Event ID	CASEID	PT
125698811	12569881	Intentional overdose
125698811	12569881	No adverse event
125698811	12569881	Suicide attempt

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
125698811	12569881	1	20160122	20160122
125698811	12569881	2	20160122	20160122
125698811	12569881	3	20160122	20160122