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
124110374	12411037	4	F	2016	20160718	20160527	20160725	EXP		US-JNJFOC-20160520509	JOHNSON AND JOHNSON		55.00	YR	A	F	Y	62.40000	KG	20160725		MD	US	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
124110374	12411037	1	PS	TYLENOL	ACETAMINOPHEN	1	Oral	TOOK 100 TABLETS OF 650 MG IN A SUICIDE ATTEMPT				N			999999	65000	MG	TABLETS
124110374	12411037	2	SS	ETHANOL	ALCOHOL	1	Unknown								0			UNSPECIFIED

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
124110374	12411037	1	Product used for unknown indication
124110374	12411037	2	Product used for unknown indication

Outcome of event

Reactions reported

Event ID	CASEID	PT
124110374	12411037	Acute hepatic failure
124110374	12411037	Brain injury
124110374	12411037	Brain oedema
124110374	12411037	Coma
124110374	12411037	Completed suicide
124110374	12411037	Drug administration error
124110374	12411037	Hepatic encephalopathy
124110374	12411037	Hepatic necrosis
124110374	12411037	Intentional overdose
124110374	12411037	Renal failure
124110374	12411037	Respiratory failure

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
124110374	12411037	1	20160520	20160520	0