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
125834601 12583460 1 I 20160609 20160722 20160722 EXP US-ELI_LILLY_AND_COMPANY-US201607008197 ELI LILLY AND CO 0.00 F Y 0.00000 20160722 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
125834601 12583460 1 PS HUMALOG INSULIN LISPRO 1 Unknown SLIDING SCALE 20563 INJECTION
125834601 12583460 2 SS HUMALOG INSULIN LISPRO 1 SLIDING SCALE C536215A 20563 INJECTION
125834601 12583460 3 C LANTUS INSULIN GLARGINE 1 15 U, UNK N 0 15 IU
125834601 12583460 4 C LANTUS INSULIN GLARGINE 1 11 U, UNK N 0 11 IU

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125834601 12583460 1 Type 1 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125834601 12583460 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125834601 12583460 Blood glucose decreased
125834601 12583460 Blood glucose increased
125834601 12583460 Cerebrovascular accident
125834601 12583460 Dawn phenomenon
125834601 12583460 Incorrect product storage

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
125834601 12583460 1 1996 0