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
122025075 12202507 5 F 20160210 20160830 20160322 20160912 EXP GB-ROCHE-1727329 ROCHE 78.69 YR F Y 0.00000 20160909 MD GB GB

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
122025075 12202507 1 PS Pertuzumab PERTUZUMAB 1 Intravenous (not otherwise specified) U 125409 420 MG SOLUTION FOR INFUSION Q3W
122025075 12202507 2 SS Pertuzumab PERTUZUMAB 1 Intravenous (not otherwise specified) U 125409 840 MG SOLUTION FOR INFUSION Q3W
122025075 12202507 3 SS Trastuzumab TRASTUZUMAB 1 Intravenous (not otherwise specified) U 103792 472.5 MG SOLUTION FOR INFUSION Q3W
122025075 12202507 4 SS Trastuzumab TRASTUZUMAB 1 Intravenous (not otherwise specified) U 103792 630 MG SOLUTION FOR INFUSION Q3W
122025075 12202507 5 SS DOCETAXEL. DOCETAXEL 1 Intravenous (not otherwise specified) PLANNED NUMBER OF CYCLES COMPLETED Y 0 94 MG Q3W
122025075 12202507 6 C TAXOTERE DOCETAXEL 1 Intravenous (not otherwise specified) CHEMOTHERAPY 0 94 MG Q3W
122025075 12202507 7 C METOCLOPRAMIDE. METOCLOPRAMIDE 1 Intravenous (not otherwise specified) 0 10 MG
122025075 12202507 8 C METOCLOPRAMIDE. METOCLOPRAMIDE 1 Intravenous (not otherwise specified) 0 10 MG
122025075 12202507 9 C DEXAMETHASONE. DEXAMETHASONE 1 Intravenous (not otherwise specified) 0 8 MG BID
122025075 12202507 10 C Filgrastim FILGRASTIM 1 Intravenous (not otherwise specified) 0 480 UG
122025075 12202507 11 C DEXAMETHASONE. DEXAMETHASONE 1 Oral 0 8 MG TABLET BID
122025075 12202507 12 C FLUCLOXACILLIN FLUCLOXACILLIN 1 Oral 0 500 MG TABLET QID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122025075 12202507 1 HER-2 positive breast cancer
122025075 12202507 3 HER-2 positive breast cancer
122025075 12202507 5 HER-2 positive breast cancer

Outcome of event

Event ID CASEID OUTC COD
122025075 12202507 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122025075 12202507 Decreased appetite
122025075 12202507 Deep vein thrombosis
122025075 12202507 Diarrhoea
122025075 12202507 Dyspepsia
122025075 12202507 Fatigue
122025075 12202507 Nausea
122025075 12202507 Peripheral swelling
122025075 12202507 Rash

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
122025075 12202507 1 20160212 0
122025075 12202507 2 20160121 20160121 0
122025075 12202507 3 20160212 0
122025075 12202507 4 20160121 20160121 0
122025075 12202507 5 20160122 20160520 0
122025075 12202507 6 20160122 0
122025075 12202507 7 20160122 20160122 0
122025075 12202507 8 20160112 20160112 0
122025075 12202507 9 20160121 20160123 0
122025075 12202507 10 20160123 20160127 0
122025075 12202507 11 20160211 20160214 0
122025075 12202507 12 20160427 0