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
126196971 12619697 1 I 201603 20160725 20160803 20160803 EXP US-SA-2016SA137362 AVENTIS 60.00 YR A F Y 0.00000 20160803 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
126196971 12619697 1 PS LANTUS SOLOSTAR INSULIN GLARGINE 1 Unknown DOSE:50 UNIT(S) 6F3200A 21081 QD
126196971 12619697 2 C SOLOSTAR DEVICE 1 0
126196971 12619697 3 C PROLIA DENOSUMAB 1 0
126196971 12619697 4 C TOUJEO INSULIN GLARGINE 1 0
126196971 12619697 5 C SOLOSTAR DEVICE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126196971 12619697 1 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126196971 12619697 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126196971 12619697 Arthritis
126196971 12619697 Gallbladder disorder
126196971 12619697 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
126196971 12619697 1 2015 0
126196971 12619697 2 2015 0
126196971 12619697 3 2016 0