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
127076981	12707698	1	I	20160602	20160602	20160901	20160901	EXP		AR-ELI_LILLY_AND_COMPANY-AR201606001905	ELI LILLY AND CO		31.31	YR		F	Y	0.00000		20160901		CN	AR	AR

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	DECHAL	RECHAL	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FREQ
127076981	12707698	1	PS	HUMULIN N	INSULIN HUMAN	1	Subcutaneous	2 U, EACH MORNING	U	U	18780	2	IU	QD
127076981	12707698	2	SS	HUMULIN N	INSULIN HUMAN	1	Subcutaneous	10 U, EACH EVENING	U	U	18780	10	IU	QD
127076981	12707698	3	C	LEVOTHYROXINE.	LEVOTHYROXINE	1		100 MG, UNK			0	100	MG

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127076981	12707698	1	Gestational diabetes
127076981	12707698	3	Hypertension

Outcome of event

Event ID	CASEID	OUTC COD
127076981	12707698	OT

Reactions reported

Event ID	CASEID	PT
127076981	12707698	Blood glucose increased
127076981	12707698	Exposure during breast feeding
127076981	12707698	Hypertension
127076981	12707698	Maternal exposure during pregnancy

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
127076981	12707698	1	20160602	20160715	0
127076981	12707698	2	20160602	20160715	0