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
115312202 11531220 2 F 2013 20160919 20150921 20160929 EXP US-SA-2015SA139803 AVENTIS 69.00 YR E F Y 0.00000 20160929 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
115312202 11531220 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown U 5F1501A 21081 INJECTION BID
115312202 11531220 2 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown 8-10U U 5F1501A 21081 INJECTION QD
115312202 11531220 3 SS HUMALOG INSULIN LISPRO 1 Unknown UNKNOWN 0
115312202 11531220 4 SS NOVOLOG INSULIN ASPART 1 Unknown U UNKNOWN 0
115312202 11531220 5 C SOLOSTAR DEVICE 1 0
115312202 11531220 6 C TOUJEO INSULIN GLARGINE 1 Unknown UNK 0
115312202 11531220 7 C SOLOSTAR DEVICE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
115312202 11531220 1 Type 1 diabetes mellitus
115312202 11531220 2 Type 1 diabetes mellitus
115312202 11531220 5 Type 1 diabetes mellitus
115312202 11531220 6 Type 1 diabetes mellitus
115312202 11531220 7 Type 1 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
115312202 11531220 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
115312202 11531220 Blood glucose decreased
115312202 11531220 Blood glucose increased
115312202 11531220 Product use issue
115312202 11531220 Vascular graft

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
115312202 11531220 1 2013 0
115312202 11531220 2 2016 0
115312202 11531220 5 2013 0