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
125006662 12500666 2 F 2014 20160628 20160627 20160706 EXP CN-ELI_LILLY_AND_COMPANY-CN201606007000 ELI LILLY AND CO 0.00 F Y 63.00000 KG 20160706 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
125006662 12500666 1 PS HUMULIN R INSULIN HUMAN 1 Subcutaneous 5 U, BID 18780 5 IU INJECTION BID
125006662 12500666 2 SS HUMULIN R INSULIN HUMAN 1 Subcutaneous 6 U, QD 18780 6 IU INJECTION QD
125006662 12500666 3 SS HUMULIN R INSULIN HUMAN 1 Subcutaneous 7 U, TID 18780 7 IU INJECTION TID
125006662 12500666 4 SS HUMULIN N INSULIN HUMAN 1 Subcutaneous 8 U, QD 0 8 IU INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125006662 12500666 1 Diabetes mellitus
125006662 12500666 4 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125006662 12500666 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125006662 12500666 Blood glucose increased
125006662 12500666 Cerebral infarction

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
125006662 12500666 1 2011 0
125006662 12500666 2 2011 0
125006662 12500666 4 2011 0