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
125917021 12591702 1 I 20160525 0 20160725 20160725 DIR 61.73 YR F N 65.40000 KG 20160720 N MD CA

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
125917021 12591702 1 PS 5-FLUOROURACIL (5-FU) FLUOROURACIL 1 D D 0 4600 MG
125917021 12591702 2 SS LEUCOVORIN CALCIUM. LEUCOVORIN CALCIUM 1 0 650 MG
125917021 12591702 3 SS ELOXATIN OXALIPLATIN 1 0 140 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125917021 12591702 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125917021 12591702 Acute kidney injury
125917021 12591702 Hyponatraemia
125917021 12591702 Mucosal discolouration
125917021 12591702 Nausea
125917021 12591702 Vomiting
125917021 12591702 Wound complication

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

Event ID CASEID RPSR COD
125917021 12591702 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125917021 12591702 1 20151027 0
125917021 12591702 2 20151027 0
125917021 12591702 3 20151027 0