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
127077171	12707717	1	I	20160803	20160826	20160901	20160901	EXP		BR-ELI_LILLY_AND_COMPANY-BR201608012951	ELI LILLY AND CO		4.39	YR		F	Y	15.20000	KG	20160901		CN	BR	BR

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	DECHAL	RECHAL	LOT NUM	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
127077171	12707717	1	PS	HUMULIN N	INSULIN HUMAN	1	Subcutaneous	6 IU, EACH MORNING	U	U		18780	6	IU	INJECTION	QD
127077171	12707717	2	SS	HUMULIN N	INSULIN HUMAN	1	Subcutaneous	2 IU, EACH EVENING	U	U		18780	2	IU	INJECTION	QD
127077171	12707717	3	SS	HUMULIN N	INSULIN HUMAN	1	Subcutaneous	6 IU, EACH MORNING	U	U	C525255C	18780	6	IU	INJECTION	QD
127077171	12707717	4	SS	HUMULIN N	INSULIN HUMAN	1	Subcutaneous	2 IU, EACH EVENING	U	U	C525255C	18780	2	IU	INJECTION	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127077171	12707717	1	Diabetes mellitus

Outcome of event

Event ID	CASEID	OUTC COD
127077171	12707717	OT

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
127077171	12707717		Blood glucose increased
127077171	12707717		Drug dose omission

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
127077171	12707717	1	20160329		0
127077171	12707717	2	20160329		0