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
125688461 12568846 1 I 20071210 20150713 20160719 20160719 EXP US-ROCHE-1674882 ROCHE 57.00 YR M Y 0.00000 20160719 MD US US

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
125688461 12568846 1 PS Pertuzumab PERTUZUMAB 1 Intravenous (not otherwise specified) U 125409 420 MG SOLUTION FOR INFUSION
125688461 12568846 2 SS CETUXIMAB CETUXIMAB 1 Intravenous (not otherwise specified) OVER 120 MIN ON DAY 2 U 0 400 MG/M**2
125688461 12568846 3 SS CETUXIMAB CETUXIMAB 1 Intravenous (not otherwise specified) OVER 120 MIN ON DAYS 8 AND 15 U 0 250 MG/M**2
125688461 12568846 4 SS IRINOTECAN IRINOTECAN 1 Intravenous (not otherwise specified) ON DAY 2 (CYCLE 1) U 0 350 MG/M**2

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125688461 12568846 1 Colorectal cancer metastatic
125688461 12568846 2 Colorectal cancer metastatic
125688461 12568846 4 Colorectal cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
125688461 12568846 OT
125688461 12568846 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125688461 12568846 Dehydration
125688461 12568846 Dermatitis acneiform
125688461 12568846 Palmar-plantar erythrodysaesthesia syndrome
125688461 12568846 Vomiting

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found