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
127386811 12738681 1 I 20160810 20160912 20160912 PER US-SA-2016SA148811 AVENTIS 75.00 YR E F Y 0.00000 20160912 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
127386811 12738681 1 PS SOLOSTAR DEVICE 1 6F293A 206538 QD
127386811 12738681 2 SS TOUJEO INSULIN GLARGINE 1 Unknown DOSE:26 UNIT(S) 6F293A 206538 QD
127386811 12738681 3 C LANTUS INSULIN GLARGINE 1 0
127386811 12738681 4 C LANTUS SOLOSTAR INSULIN GLARGINE 1 0
127386811 12738681 5 C SOLOSTAR DEVICE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127386811 12738681 1 Type 1 diabetes mellitus
127386811 12738681 2 Type 1 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127386811 12738681 Blood glucose fluctuation
127386811 12738681 Device issue
127386811 12738681 Hyperhidrosis
127386811 12738681 Hypoglycaemia

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
127386811 12738681 1 2015 0
127386811 12738681 2 2015 0