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
101880823 10188082 3 F 20160830 20140522 20160908 EXP US-SA-2013SA098670 AVENTIS 59.00 YR A M Y 74.84000 KG 20160908 OT 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
101880823 10188082 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:24 UNIT(S) 3F102A 21081 SOLUTION FOR INJECTION QD
101880823 10188082 2 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:24 UNIT(S) 5F2033A 21081 SOLUTION FOR INJECTION QD
101880823 10188082 3 C SOLOSTAR DEVICE 1 0 QD
101880823 10188082 4 C CARVEDILOL. CARVEDILOL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101880823 10188082 1 Type 2 diabetes mellitus
101880823 10188082 2 Type 2 diabetes mellitus
101880823 10188082 3 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
101880823 10188082 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
101880823 10188082 Intentional product misuse
101880823 10188082 Product use issue
101880823 10188082 Renal disorder
101880823 10188082 Visual acuity reduced

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
101880823 10188082 1 2013 0
101880823 10188082 2 2013 0
101880823 10188082 3 2013 0