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
125196432 12519643 2 F 20160510 20160630 20160701 20160704 EXP IT-ROCHE-1786686 ROCHE 60.89 YR F Y 0.00000 20160704 OT IT IT

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
125196432 12519643 1 PS AVASTIN BEVACIZUMAB 1 Intravenous (not otherwise specified) LAST DOSE PRIOR TO SAE: 27/APR/2016 Y B7054H06 125085 500 MG
125196432 12519643 2 SS AVASTIN BEVACIZUMAB 1 Intravenous (not otherwise specified) Y B7054H06 125085 500 MG
125196432 12519643 3 SS PACLITAXEL. PACLITAXEL 1 Intravenous (not otherwise specified) LAST DOSE PRIOR TO SAE: 27/APR/2016 Y 0 132 MG
125196432 12519643 4 SS PACLITAXEL. PACLITAXEL 1 Intravenous (not otherwise specified) Y 0 132 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125196432 12519643 1 Breast cancer
125196432 12519643 3 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
125196432 12519643 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125196432 12519643 Anaemia
125196432 12519643 Thrombocytopenia

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
125196432 12519643 1 20160414 0
125196432 12519643 2 20160609 0
125196432 12519643 3 20160414 0
125196432 12519643 4 20160609 0