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
125274362 12527436 2 F 20160718 20160705 20160727 EXP BR-ELI_LILLY_AND_COMPANY-BR201606009120 ELI LILLY AND CO 0.00 M Y 0.00000 20160726 CN BR BR

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
125274362 12527436 1 PS HUMULIN N INSULIN HUMAN 1 Subcutaneous 60 IU, EACH MORNING U U 18780 60 IU INJECTION QD
125274362 12527436 2 SS HUMULIN N INSULIN HUMAN 1 Subcutaneous 60 IU, EACH EVENING U U 18780 60 IU INJECTION QD
125274362 12527436 3 SS HUMULIN N INSULIN HUMAN 1 Subcutaneous 60 IU, EACH MORNING U U C589028 18780 60 IU INJECTION QD
125274362 12527436 4 SS HUMULIN N INSULIN HUMAN 1 Subcutaneous 60 IU, EACH EVENING U U C589028 18780 60 IU INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125274362 12527436 1 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125274362 12527436 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125274362 12527436 Drug ineffective
125274362 12527436 Expired product administered
125274362 12527436 Injury
125274362 12527436 Malabsorption from administration site

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
125274362 12527436 1 2006 0
125274362 12527436 2 2006 0