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
127380551 12738055 1 I 20160818 20160912 20160912 PER US-SA-2016SA154490 AVENTIS 0.00 A 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
127380551 12738055 1 PS TOUJEO INSULIN GLARGINE 1 Unknown U UNK 206538
127380551 12738055 2 SS JANUVIA SITAGLIPTIN PHOSPHATE 1 Unknown U UNK 0
127380551 12738055 3 C SOLOSTAR DEVICE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127380551 12738055 1 Diabetes mellitus
127380551 12738055 3 Diabetes mellitus

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127380551 12738055 Blood glucose decreased
127380551 12738055 Blood glucose increased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found