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
126518241 12651824 1 I 20160730 20160801 20160815 20160815 EXP DE-SA-2016SA141444 AVENTIS 46.00 YR A M Y 0.00000 20160815 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
126518241 12651824 1 PS OXALIPLATIN. OXALIPLATIN 1 Unknown U UNK 21759
126518241 12651824 2 SS BEVACIZUMAB BEVACIZUMAB 1 Unknown U UNK 0
126518241 12651824 3 SS LEUCOVORIN. LEUCOVORIN 1 Unknown U UNK 0
126518241 12651824 4 SS IRINOTECAN IRINOTECAN 1 0
126518241 12651824 5 SS 5-FU FLUOROURACIL 1 Unknown U UNK 0
126518241 12651824 6 SS 5-FU FLUOROURACIL 1 Unknown U UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126518241 12651824 1 Colorectal cancer metastatic
126518241 12651824 2 Colorectal cancer metastatic
126518241 12651824 3 Colorectal cancer metastatic
126518241 12651824 5 Colorectal cancer metastatic
126518241 12651824 6 Colorectal cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
126518241 12651824 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126518241 12651824 Abdominal pain lower
126518241 12651824 Constipation
126518241 12651824 Pyrexia

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

no results found

Therapies reported

no results found