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
127386921 12738692 1 I 20160804 20160912 20160912 PER US-SA-2016SA149955 AVENTIS 50.00 YR A M Y 0.00000 20160912 PH 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
127386921 12738692 1 PS SOLOSTAR DEVICE 1 6F246A 206538 QD
127386921 12738692 2 SS SOLOSTAR DEVICE 1 UNKNOWN 206538 QD
127386921 12738692 3 SS TOUJEO INSULIN GLARGINE 1 Unknown DOSE:80 UNIT(S) 6F246A 206538 SOLUTION FOR INJECTION QD
127386921 12738692 4 SS TOUJEO INSULIN GLARGINE 1 Unknown DOSE:80 UNIT(S) UNKNOWN 206538 SOLUTION FOR INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127386921 12738692 1 Type 2 diabetes mellitus
127386921 12738692 2 Type 2 diabetes mellitus
127386921 12738692 3 Type 2 diabetes mellitus
127386921 12738692 4 Type 2 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127386921 12738692 Blood glucose decreased
127386921 12738692 Wrong technique in product usage process

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
127386921 12738692 1 20151114 0
127386921 12738692 2 20151114 0
127386921 12738692 3 20151114 0
127386921 12738692 4 20151114 0