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
127080191 12708019 1 I 20160822 20160901 20160901 EXP US-SA-2016SA155872 AVENTIS 55.00 YR A F Y 0.00000 20160901 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
127080191 12708019 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:34 UNIT(S) U 4F1269A 21081
127080191 12708019 2 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:28 UNIT(S) U 4F1269A 21081
127080191 12708019 3 SS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:22 UNIT(S) U 4F1269A 21081 QD
127080191 12708019 4 C SOLOSTAR DEVICE 1 DOSE:34 UNIT(S) 4F1269A 0
127080191 12708019 5 C SOLOSTAR DEVICE 1 DOSE:28 UNIT(S) 4F1269A 0
127080191 12708019 6 C SOLOSTAR DEVICE 1 DOSE:22 UNIT(S) 4F1269A 0 QD
127080191 12708019 7 C LANTUS INSULIN GLARGINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127080191 12708019 1 Type 1 diabetes mellitus
127080191 12708019 2 Type 1 diabetes mellitus
127080191 12708019 3 Type 1 diabetes mellitus
127080191 12708019 4 Type 1 diabetes mellitus
127080191 12708019 5 Type 1 diabetes mellitus
127080191 12708019 6 Type 1 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
127080191 12708019 HO
127080191 12708019 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127080191 12708019 Diabetic complication
127080191 12708019 Limb injury
127080191 12708019 Renal disorder

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
127080191 12708019 1 2007 0
127080191 12708019 4 2007 0