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
116693162 11669316 2 F 201512 20160901 20151027 20160913 EXP US-ELI_LILLY_AND_COMPANY-US201510006572 ELI LILLY AND CO 74.38 YR F Y 0.00000 20160913 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
116693162 11669316 1 SS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 25 U, PRN 0 25 IU INJECTION
116693162 11669316 2 SS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 25 U, PRN C370889A 0 25 IU INJECTION
116693162 11669316 3 SS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 35 U, PRN C558467A 0 35 IU INJECTION
116693162 11669316 4 SS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 35 U, PRN 0 35 IU INJECTION
116693162 11669316 5 PS HUMALOG INSULIN LISPRO 1 Unknown 25 U, TID U U C428126A 20563 25 IU INJECTION TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116693162 11669316 1 Type 2 diabetes mellitus
116693162 11669316 5 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
116693162 11669316 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116693162 11669316 Blood glucose increased
116693162 11669316 Incorrect product storage
116693162 11669316 Weight increased

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
116693162 11669316 1 2014 0