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
125855002 12585500 2 F 2013 20160815 20160724 20160826 EXP US-ELI_LILLY_AND_COMPANY-US201607005143 ELI LILLY AND CO 0.00 F Y 0.00000 20160825 MD 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
125855002 12585500 1 PS Insulin Human INSULIN HUMAN 1 Unknown 18 U, EACH MORNING U U 18780 18 IU INJECTION QD
125855002 12585500 2 SS Insulin Human INSULIN HUMAN 1 Unknown 15 U, QD U U 18780 15 IU INJECTION QD
125855002 12585500 3 SS Insulin Human INSULIN HUMAN 1 Unknown 8 U, EACH EVENING U U 18780 8 IU INJECTION QD
125855002 12585500 4 SS HUMULIN N INSULIN HUMAN 1 Unknown UNK, UNKNOWN U U 0
125855002 12585500 5 C SINVASTATINA SIMVASTATIN 1 U 0
125855002 12585500 6 C QUINAPRIL. QUINAPRIL 1 U 0
125855002 12585500 7 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125855002 12585500 1 Diabetes mellitus
125855002 12585500 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125855002 12585500 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125855002 12585500 Blindness

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
125855002 12585500 1 2012 0
125855002 12585500 2 2012 0
125855002 12585500 3 2012 0