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
82298324 8229832 4 F 20111016 20160707 20111104 20160712 EXP FR-ROCHE-1007124 ROCHE 76.99 YR F Y 0.00000 20160713 MD FR FR

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
82298324 8229832 1 PS Bevacizumab BEVACIZUMAB 1 Unknown Y 125085 10 MG/KG SOLUTION FOR INFUSION
82298324 8229832 2 SS CAPECITABINE. CAPECITABINE 1 Unknown Y 20896 1600 MG/M**2 TABLET
82298324 8229832 3 SS PACLITAXEL. PACLITAXEL 1 Unknown 0 80 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
82298324 8229832 1 Breast cancer
82298324 8229832 2 Breast cancer
82298324 8229832 3 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
82298324 8229832 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
82298324 8229832 Cardiac arrest
82298324 8229832 Dyspnoea

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
82298324 8229832 1 20110819 20111014 0
82298324 8229832 2 20110421 20111004 0
82298324 8229832 3 20110421 20110930 0