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
125380891 12538089 1 I 20160630 20160707 20160707 EXP US-SA-2016SA123419 AVENTIS 55.00 YR A M Y 0.00000 20160707 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
125380891 12538089 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:30 UNIT(S) UNKNOWN 21081 QD
125380891 12538089 2 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:30 UNIT(S) UNKNOWN 21081 QD
125380891 12538089 3 C SOLOSTAR DEVICE 1 0
125380891 12538089 4 C SOLOSTAR DEVICE 1 0
125380891 12538089 5 C HUMALOG INSULIN LISPRO 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125380891 12538089 1 Type 2 diabetes mellitus
125380891 12538089 2 Type 2 diabetes mellitus
125380891 12538089 3 Type 2 diabetes mellitus
125380891 12538089 4 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125380891 12538089 DS
125380891 12538089 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125380891 12538089 Cerebrovascular accident
125380891 12538089 Condition aggravated
125380891 12538089 Disability
125380891 12538089 Drug dose omission
125380891 12538089 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
125380891 12538089 1 2015 0
125380891 12538089 3 2015 0