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
125224681 12522468 1 I 20160627 20160701 20160701 PER US-ELI_LILLY_AND_COMPANY-US201606010370 ELI LILLY AND CO 0.00 F Y 0.00000 20160701 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
125224681 12522468 1 PS HUMALOG INSULIN LISPRO 1 Unknown UNK, UNKNOWN 205747 INJECTION
125224681 12522468 2 SS HUMALOG INSULIN LISPRO 1 Unknown UNK, UNKNOWN C446949C 205747 INJECTION
125224681 12522468 3 C LANTUS INSULIN GLARGINE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125224681 12522468 1 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125224681 12522468 Visual impairment

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
125224681 12522468 1 2006 0