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
125360931 12536093 1 I 201507 20140915 20160707 20160707 EXP US-ELI_LILLY_AND_COMPANY-US201409005903 ELI LILLY AND CO 75.84 YR F Y 0.00000 20160706 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
125360931 12536093 1 PS HUMALOG INSULIN LISPRO 1 Unknown UNK UNK, PRN C175102A 20563 INJECTION
125360931 12536093 2 SS HUMALOG INSULIN LISPRO 1 Unknown UNK UNK, PRN C522521F 20563 INJECTION
125360931 12536093 3 C LANTUS INSULIN GLARGINE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125360931 12536093 1 Type 2 diabetes mellitus
125360931 12536093 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125360931 12536093 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125360931 12536093 Diabetic retinal oedema
125360931 12536093 Incorrect product storage

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
125360931 12536093 1 2006 0
125360931 12536093 2 2006 0