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
125515103 12551510 3 F 20160202 20160721 20160713 20160729 EXP 365704 IT-ACCORD-042259 ACCORD 65.00 YR M Y 88.00000 KG 20160729 MD 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
125515103 12551510 1 PS CAPECITABINE. CAPECITABINE 1 Oral THE PATIENT UNDERWENT CYCLE 5 AND 7 XELOX 202593 2000 MG TABLET
125515103 12551510 2 SS OXALIPLATIN. OXALIPLATIN 1 Intravenous (not otherwise specified) THE PATIENT UNDERWENT CYCLE 5 AND 7 XELOX 200750096 160 MG SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125515103 12551510 1 Adenocarcinoma of colon
125515103 12551510 2 Adenocarcinoma of colon

Outcome of event

Event ID CASEID OUTC COD
125515103 12551510 OT
125515103 12551510 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125515103 12551510 Dizziness
125515103 12551510 Fall
125515103 12551510 Pain in extremity
125515103 12551510 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
125515103 12551510 1 20151009 0
125515103 12551510 2 20151009 0