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
125869671 12586967 1 I 20160413 20160419 20160725 20160725 EXP JP-ROCHE-1746683 ROCHE 76.00 YR M Y 0.00000 20160725 MD JP JP

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
125869671 12586967 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous drip DOSAGE IS UNCERTAIN. ?OUTSIDE COURSE 125085 SOLUTION FOR INFUSION
125869671 12586967 2 SS CAPECITABINE. CAPECITABINE 1 Oral DOSAGE IS UNCERTAIN. ?OUTSIDE COURSE 20896 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125869671 12586967 1 Colon cancer
125869671 12586967 2 Colon cancer

Outcome of event

Event ID CASEID OUTC COD
125869671 12586967 DE
125869671 12586967 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125869671 12586967 Colitis ischaemic
125869671 12586967 Duodenal perforation
125869671 12586967 Gastrointestinal necrosis
125869671 12586967 Large intestine perforation
125869671 12586967 Peritonitis
125869671 12586967 Sepsis
125869671 12586967 Small intestinal perforation

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
125869671 12586967 1 20151201 2016 0
125869671 12586967 2 20151201 2016 0