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
119842532 11984253 2 F 2014 20160706 20160201 20160714 EXP US-SA-2016SA014612 AVENTIS 58.00 YR A M Y 76.20000 KG 20160714 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
119842532 11984253 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:30 UNIT(S) 5F2060A 21081 INJECTION QD
119842532 11984253 2 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:30 UNIT(S) UNKNOWN 21081 INJECTION QD
119842532 11984253 3 C SOLOSTAR DEVICE 1 5F2060A 0 QD
119842532 11984253 4 C SOLOSTAR DEVICE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119842532 11984253 1 Type 2 diabetes mellitus
119842532 11984253 2 Type 2 diabetes mellitus
119842532 11984253 3 Type 2 diabetes mellitus
119842532 11984253 4 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
119842532 11984253 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119842532 11984253 Cerebrovascular accident
119842532 11984253 Visual impairment

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found