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
109119593 10911959 3 F 2013 20160829 20150313 20160907 EXP US-SA-2015SA028589 AVENTIS 0.00 A M Y 0.00000 20160907 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
109119593 10911959 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE: 24 U A.M./20 U P.M. 4F494A 21081 INJECTION BID
109119593 10911959 2 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE: 24 U A.M./20 U P.M. 6F2948A 21081 INJECTION BID
109119593 10911959 3 C SOLOSTAR DEVICE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109119593 10911959 1 Type 2 diabetes mellitus
109119593 10911959 2 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
109119593 10911959 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
109119593 10911959 Cerebrovascular accident
109119593 10911959 Product use issue
109119593 10911959 Thrombosis

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
109119593 10911959 1 2013 0
109119593 10911959 2 2013 0
109119593 10911959 3 2013 0