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
125661443	12566144	3	F	20160709	20160802	20160718	20160808	EXP		BR-ELI_LILLY_AND_COMPANY-BR201607004352	ELI LILLY AND CO		11.36	YR		M	Y	47.00000	KG	20160808		CN	BR	BR

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	DECHAL	LOT NUM	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
125661443	12566144	1	PS	HUMALOG	INSULIN LISPRO	1	Subcutaneous	UNK UNK, OTHER		C464985A	20563			INJECTION
125661443	12566144	2	SS	HUMALOG	INSULIN LISPRO	1	Subcutaneous	UNK UNK, QD		C459940A	20563			INJECTION	QD
125661443	12566144	3	C	LANTUS	INSULIN GLARGINE	1	Unknown	22 IU, EACH MORNING	U		0	22	IU		QD
125661443	12566144	4	C	LANTUS	INSULIN GLARGINE	1	Unknown	24 IU, EACH MORNING	U		0	24	IU		QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125661443	12566144	1	Product used for unknown indication
125661443	12566144	3	Product used for unknown indication

Outcome of event

Event ID	CASEID	OUTC COD
125661443	12566144	OT

Reactions reported

Event ID	CASEID	PT
125661443	12566144	Hyperglycaemia
125661443	12566144	Nervousness
125661443	12566144	Underdose

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
125661443	12566144	1	20160705		0