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
125726621 12572662 1 I 20140401 20160720 20160720 EXP US-ROCHE-1376858 ROCHE 0.00 Y 0.00000 20160720 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
125726621 12572662 1 PS Pertuzumab PERTUZUMAB 1 Intravenous (not otherwise specified) OVER 30-60 MINUTES ON DAY 1 U 125409 210 MG
125726621 12572662 2 SS Pertuzumab PERTUZUMAB 1 U 125409
125726621 12572662 3 SS CETUXIMAB CETUXIMAB 1 Intravenous (not otherwise specified) OVER 120 MIN ON DAY 2 FOLLOWED BY 250MG/M2 IV OVER 60 MIN ON DAYS 8 AND 15 (CYCLE 1)?OVER 60-120 MIN U 0 250 MG/M**2
125726621 12572662 4 SS CETUXIMAB CETUXIMAB 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125726621 12572662 1 Colon cancer
125726621 12572662 2 Rectal cancer
125726621 12572662 3 Colon cancer
125726621 12572662 4 Rectal cancer

Outcome of event

Event ID CASEID OUTC COD
125726621 12572662 OT
125726621 12572662 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125726621 12572662 Dyspnoea
125726621 12572662 Hypokalaemia
125726621 12572662 Lung infection
125726621 12572662 Myocardial infarction
125726621 12572662 Stomatitis
125726621 12572662 Troponin I increased

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

no results found

Therapies reported

no results found