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
127379011 12737901 1 I 20160603 20160912 20160912 PER US-SA-2016SA108557 AVENTIS 61.00 YR A 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
127379011 12737901 1 PS SOLOSTAR DEVICE 1 5F071A 206538 QD
127379011 12737901 2 SS TOUJEO INSULIN GLARGINE 1 Unknown DOSE:15 UNIT(S) 5F071A 206538 SOLUTION FOR INJECTION QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127379011 12737901 1 Type 1 diabetes mellitus
127379011 12737901 2 Type 1 diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127379011 12737901 Blood glucose increased
127379011 12737901 Device issue
127379011 12737901 Injection site pain
127379011 12737901 Weight decreased

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
127379011 12737901 1 2015 0
127379011 12737901 2 2015 0