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
124006174 12400617 4 F 2007 20151009 20160525 20160920 EXP US-SA-2015SA160901 AVENTIS 63.00 YR A F Y 0.00000 20160920 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
124006174 12400617 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown 60U IN AM/ 20 U PM 5F1478A 21081 INJECTION BID
124006174 12400617 2 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown 60U IN AM/ 20 U PM 3F331A 21081 INJECTION BID
124006174 12400617 3 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown 60U IN AM/ 20 U PM 4F1998A 21081 INJECTION BID
124006174 12400617 4 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown 60U IN AM/ 20 U PM 5F1478A 21081 INJECTION BID
124006174 12400617 5 C SOLOSTAR DEVICE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124006174 12400617 1 Type 2 diabetes mellitus
124006174 12400617 2 Type 2 diabetes mellitus
124006174 12400617 3 Type 2 diabetes mellitus
124006174 12400617 4 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
124006174 12400617 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124006174 12400617 Condition aggravated
124006174 12400617 Drug administration error
124006174 12400617 Mental impairment
124006174 12400617 Visual impairment
124006174 12400617 Wrong technique in product usage process

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
124006174 12400617 1 2007 0
124006174 12400617 2 2007 0
124006174 12400617 3 2007 0
124006174 12400617 4 2007 0