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
125896501 12589650 1 I 2016 20160719 20160725 20160725 PER US-ELI_LILLY_AND_COMPANY-US201607008104 ELI LILLY AND CO 0.00 F Y 0.00000 20160725 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
125896501 12589650 1 PS HUMALOG INSULIN LISPRO 1 Unknown 15 U, EACH MORNING Y U 20563 15 IU INJECTION QD
125896501 12589650 2 SS HUMALOG INSULIN LISPRO 1 Unknown 15 U, EACH EVENING Y U 20563 15 IU INJECTION QD
125896501 12589650 3 SS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 15 U, EACH MORNING C503107E 0 15 IU INJECTION QD
125896501 12589650 4 SS HUMALOG MIX75/25 INSULIN LISPRO 1 Unknown 12 U, EACH EVENING C503107E 0 12 IU INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125896501 12589650 1 Type 2 diabetes mellitus
125896501 12589650 3 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125896501 12589650 Blood glucose abnormal
125896501 12589650 Rash

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
125896501 12589650 1 201603 0
125896501 12589650 2 201603 0
125896501 12589650 3 201604 0
125896501 12589650 4 201604 0