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
124359153	12435915	3	F		20160708	20160604	20160715	EXP		HK-ASTRAZENECA-2016SE57270	ASTRAZENECA		63.00	YR		F	Y	56.80000	KG	20160715		MD	HK	HK

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	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
124359153	12435915	1	PS	TAGRISSO	OSIMERTINIB	1	Oral		1840	MG		U	208065	80	MG	TABLET	QD
124359153	12435915	2	SS	IRESSA	GEFITINIB	1	Oral	DOSE UNKNOWN			U	U	0			TABLET
124359153	12435915	3	C	HERBAL MEDICINE		2							0

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
124359153	12435915	1	Lung neoplasm malignant
124359153	12435915	2	Skin reaction

Outcome of event

Event ID	CASEID	OUTC COD
124359153	12435915	DE
124359153	12435915	OT

Reactions reported

Event ID	CASEID	PT
124359153	12435915	Acute hepatic failure
124359153	12435915	Klebsiella test positive
124359153	12435915	Rash
124359153	12435915	Sepsis

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
124359153	12435915	1	20160402	20160424	0