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
125402411 12540241 1 I 201606 20160701 20160708 20160708 PER US-ELI_LILLY_AND_COMPANY-US201607001408 ELI LILLY AND CO 0.00 F Y 0.00000 20160708 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
125402411 12540241 1 PS HUMALOG INSULIN LISPRO 1 Unknown 20 U, EACH MORNING C453929E 205747 20 IU INJECTION QD
125402411 12540241 2 SS HUMALOG INSULIN LISPRO 1 Unknown UNK, UNKNOWN U U C443105E 0 INJECTION
125402411 12540241 3 C LANTUS INSULIN GLARGINE 1 60 U, EACH MORNING U 0 60 IU QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125402411 12540241 1 Type 2 diabetes mellitus
125402411 12540241 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125402411 12540241 Blood glucose decreased
125402411 12540241 Blood glucose increased
125402411 12540241 Intercepted product selection error

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
125402411 12540241 1 2015 0