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
126470901 12647090 1 I 20151007 20160812 20160812 EXP JP-CIPLA LTD.-2016JP17177 CIPLA DOI T, YOSHINO T, FUSE N, BOKU N, YAMAZAKI K, KOIZUMI W ET AL. PHASE I STUDY OF TAS-102 AND IRINOTECAN COMBINATION THERAPY IN JAPANESE PATIENTS WITH ADVANCED COLORECTAL CANCER. INVEST NEW DRUGS. 2015;33:1068 TO 1077 0.00 Y 0.00000 20160812 OT 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
126470901 12647090 1 PS Irinotecan IRINOTECAN 1 Intravenous (not otherwise specified) 150 MG/M2, OVER AT LEAST 90 MIN ON DAYS 1 AND 15 IN A 28-DAY CYCLE Y U 0 150 MG/M**2 INFUSION
126470901 12647090 2 SS OXALIPLATIN. OXALIPLATIN 1 Unknown UNK 0
126470901 12647090 3 SS TAS-102 TIPIRACIL HYDROCHLORIDETRIFLURIDINE 1 Unknown 50 MG/M2/DAY, BID Y U 0 BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126470901 12647090 1 Colorectal cancer
126470901 12647090 2 Colorectal cancer
126470901 12647090 3 Colorectal cancer

Outcome of event

Event ID CASEID OUTC COD
126470901 12647090 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126470901 12647090 Disease progression
126470901 12647090 Febrile neutropenia
126470901 12647090 Neutropenia

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

no results found

Therapies reported

no results found