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
125947613 12594761 3 F 2014 20160902 20160726 20160908 EXP CN-ELI_LILLY_AND_COMPANY-CN201607008183 ELI LILLY AND CO 64.00 YR F Y 0.00000 20160908 CN CN CN

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
125947613 12594761 1 PS HUMULIN 70/30 INSULIN HUMAN 1 Subcutaneous 20 U, QD 18780 20 IU INJECTION QD
125947613 12594761 2 SS HUMULIN 70/30 INSULIN HUMAN 1 Subcutaneous 20 DF, EACH MORNING 18780 20 DF INJECTION QD
125947613 12594761 3 SS HUMULIN 70/30 INSULIN HUMAN 1 Subcutaneous 14 U, EACH EVENING 18780 14 IU INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125947613 12594761 1 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125947613 12594761 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125947613 12594761 Arthritis
125947613 12594761 Blood glucose abnormal
125947613 12594761 Blood glucose increased
125947613 12594761 Cataract
125947613 12594761 Diabetes mellitus

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
125947613 12594761 1 2006 0