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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126403441 | 12640344 | 1 | I | 20160712 | 0 | 20160809 | 20160809 | DIR | 57.78 | YR | M | N | 77.60000 | KG | 20160803 | N | MD | US |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126403441 | 12640344 | 1 | PS | 5-FLUOROURACIL (5-FU) | FLUOROURACIL | 1 | 0 | 57106 | MG | ||||||||||
126403441 | 12640344 | 2 | SS | LEUCOVORIN CALCIUM. | LEUCOVORIN CALCIUM | 1 | 0 | 6304 | MG | ||||||||||
126403441 | 12640344 | 3 | SS | ELOXATIN | OXALIPLATIN | 1 | 0 | 1122.2 | MG |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126403441 | 12640344 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126403441 | 12640344 | Abdominal pain | |
126403441 | 12640344 | Bile duct stone | |
126403441 | 12640344 | Chest pain | |
126403441 | 12640344 | Haemangioma | |
126403441 | 12640344 | Hepatic steatosis | |
126403441 | 12640344 | Pancreatitis |
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 |
---|---|---|---|---|---|---|
126403441 | 12640344 | 1 | 20151116 | 0 | ||
126403441 | 12640344 | 2 | 20160705 | 0 | ||
126403441 | 12640344 | 3 | 20160613 | 0 |