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
93760911 9376091 1 I 201306 20130619 20130630 20130630 EXP BR-SANOFI-AVENTIS-2013SA062653 AVENTIS 82.00 YR F Y 64.00000 KG 20130630 CN BR BR

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
93760911 9376091 1 PS CLEXANE 1 DOSE: 1 SYRINGE DAILY?ROUTE: INJECTION ON BUTTOCK D 2SN44 20164 40 G SOLUTION FOR INJECTION QD
93760911 9376091 2 C LANTUS 1 D 0
93760911 9376091 3 C INSULIN 1 FROM: ABOUT 7 YEARS AGO D 0
93760911 9376091 4 C SELOZOK 1 ORAL FROM: ABOUT THREE YEARS AGO?DOSE: UNSPECIFIED DOSE IN THE MORNING D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
93760911 9376091 1 Product used for unknown indication
93760911 9376091 3 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
93760911 9376091 HO
93760911 9376091 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
93760911 9376091 Drug administered at inappropriate site
93760911 9376091 Malaise
93760911 9376091 Pulmonary embolism

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
93760911 9376091 1 20130605 20130606 0
93760911 9376091 2 20130606 0
93760911 9376091 3 20130606 0