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
126281582 12628158 2 F 20160802 20160902 20160808 20160912 EXP DE-ROCHE-1808874 ROCHE 0.00 F Y 51.00000 KG 20160912 MD DE DE

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
126281582 12628158 1 PS Pertuzumab PERTUZUMAB 1 Intravenous (not otherwise specified) 125409 420 MG SOLUTION FOR INFUSION Q3W
126281582 12628158 2 SS Trastuzumab TRASTUZUMAB 1 Intravenous (not otherwise specified) 103792 6 MG/KG SOLUTION FOR INFUSION Q3W
126281582 12628158 3 SS DOCETAXEL. DOCETAXEL 1 Intravenous (not otherwise specified) 0 75 MG/M**2 Q3W

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126281582 12628158 1 HER-2 positive breast cancer
126281582 12628158 2 HER-2 positive breast cancer
126281582 12628158 3 HER-2 positive breast cancer

Outcome of event

Event ID CASEID OUTC COD
126281582 12628158 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126281582 12628158 Dysphagia
126281582 12628158 Leukopenia

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
126281582 12628158 1 20160725 0
126281582 12628158 2 20160725 0
126281582 12628158 3 20160725 0