The Safety Rates Drug Report

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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
125064392 12506439 2 F 20160608 20160720 20160628 20160727 EXP US-ELI_LILLY_AND_COMPANY-US201606008791 ELI LILLY AND CO 45.00 YR M Y 131.61000 KG 20160727 CN 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
125064392 12506439 1 PS Insulin Human INSULIN HUMAN 1 Subcutaneous 45 U, EACH MORNING U U 18780 45 IU INJECTION QD
125064392 12506439 2 SS Insulin Human INSULIN HUMAN 1 Subcutaneous 45 U, QD U U 18780 45 IU INJECTION QD
125064392 12506439 3 SS Insulin Human INSULIN HUMAN 1 Subcutaneous 40 U, EACH EVENING U U 18780 40 IU INJECTION QD
125064392 12506439 4 SS Insulin Human INSULIN HUMAN 1 Subcutaneous 45 U, EACH MORNING U U 0 45 IU INJECTION QD
125064392 12506439 5 SS Insulin Human INSULIN HUMAN 1 Subcutaneous 45 U, QD U U 0 45 IU INJECTION QD
125064392 12506439 6 SS Insulin Human INSULIN HUMAN 1 Subcutaneous 40 U, EACH EVENING U U 0 40 IU INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125064392 12506439 1 Type 2 diabetes mellitus
125064392 12506439 4 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125064392 12506439 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125064392 12506439 Death

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125064392 12506439 1 201604 0
125064392 12506439 2 201604 0
125064392 12506439 3 201604 0
125064392 12506439 4 201604 0
125064392 12506439 5 201604 0
125064392 12506439 6 201604 0