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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123094882 | 12309488 | 2 | F | 20160722 | 20160427 | 20160809 | PER | US-PFIZER INC-2016151494 | PFIZER | 48.00 | YR | M | Y | 76.00000 | KG | 20160809 | OT | US | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123094882 | 12309488 | 1 | PS | SUTENT | SUNITINIB MALATE | 1 | Oral | 50 MG, CYCLIC (4 WEEKS ON/2 WEEKS OFF, DAYS 1-28 EVERY 42 DAYS ) | U | 595BA | 21938 | 50 | MG | CAPSULE, HARD | |||||
123094882 | 12309488 | 2 | SS | SUTENT | SUNITINIB MALATE | 1 | 37.5 MG, UNK | U | 21938 | 37.5 | MG | CAPSULE, HARD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
123094882 | 12309488 | 1 | Gastrointestinal stromal tumour |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
123094882 | 12309488 | Diarrhoea | |
123094882 | 12309488 | Drug dose omission | |
123094882 | 12309488 | Dry skin | |
123094882 | 12309488 | Pain in extremity | |
123094882 | 12309488 | Peripheral swelling |
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 |
---|---|---|---|---|---|---|
123094882 | 12309488 | 1 | 20151029 | 0 | ||
123094882 | 12309488 | 2 | 20160722 | 0 |