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
127383201 12738320 1 I 20160713 20160912 20160912 PER US-SA-2016SA130764 AVENTIS 0.00 A M 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
127383201 12738320 1 PS APIDRA SOLOSTAR INSULIN GLULISINE 1 Unknown DOSE: SSI UPTO 4 TIMES A DAY 5F255A 21629 SOLUTION FOR INJECTION
127383201 12738320 2 SS TOUJEO INSULIN GLARGINE 1 Unknown DOSE:26 UNIT(S) U 5F192A 206538 QD
127383201 12738320 3 C SOLOSTAR DEVICE 1 DOSE: SSI UPTO 4 TIMES A DAY 5F255A 0
127383201 12738320 4 C SOLOSTAR DEVICE 1 5F192A 0 QD
127383201 12738320 5 C LANTUS INSULIN GLARGINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127383201 12738320 1 Diabetes mellitus
127383201 12738320 2 Diabetes mellitus
127383201 12738320 3 Diabetes mellitus
127383201 12738320 4 Diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127383201 12738320 Blood glucose increased
127383201 12738320 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
127383201 12738320 2 201605 0
127383201 12738320 4 201605 0