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 |