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
127915891 12791589 1 I 2001 20160919 20160929 20160929 EXP US-SA-2016SA174587 AVENTIS 66.00 YR E F Y 0.00000 20160929 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
127915891 12791589 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:70 UNIT(S) 6F3431A 21081 BID
127915891 12791589 2 SS SOLOSTAR DEVICE 1 6F3431A 0 BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127915891 12791589 1 Type 2 diabetes mellitus
127915891 12791589 2 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
127915891 12791589 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127915891 12791589 Arthropathy
127915891 12791589 Blood glucose increased
127915891 12791589 Device issue
127915891 12791589 Fall
127915891 12791589 Haematoma
127915891 12791589 Product use issue
127915891 12791589 Pulmonary embolism

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
127915891 12791589 1 1998 0
127915891 12791589 2 1998 0