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
123522873 12352287 3 F 2013 20160816 20160510 20160822 EXP US-SA-2016SA088096 AVENTIS 77.00 YR E F Y 81.64000 KG 20160822 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
123522873 12352287 1 SS SOLOSTAR DEVICE 1 5F323A 0 TID
123522873 12352287 2 PS APIDRA SOLOSTAR INSULIN GLULISINE 1 Unknown DOSE:2-10 UNITS?DAILY DOSE: 6-30 UNIT 5F323A 21629 INJECTION TID
123522873 12352287 3 SS LANTUS INSULIN GLARGINE 1 Unknown U UNK 21081

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123522873 12352287 1 Type 1 diabetes mellitus
123522873 12352287 2 Type 1 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
123522873 12352287 HO
123522873 12352287 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123522873 12352287 Arthropathy
123522873 12352287 Cardiac failure congestive
123522873 12352287 Device issue
123522873 12352287 Hyperglycaemia
123522873 12352287 Myocardial infarction

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
123522873 12352287 1 2001 0
123522873 12352287 2 2001 0