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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
104509602 | 10450960 | 2 | F | 20150127 | 20140912 | 20160812 | EXP | IE-PFIZER INC-2014249788 | PFIZER | 0.00 | M | Y | 0.00000 | 20160812 | CN | IE | IE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
104509602 | 10450960 | 1 | PS | SUTENT | SUNITINIB MALATE | 1 | 50 MG, CYCLIC (4/1) | 21938 | 50 | MG | CAPSULE, HARD | ||||||||
104509602 | 10450960 | 2 | SS | SUTENT | SUNITINIB MALATE | 1 | 50 MG, CYCLIC (4/2) | 21938 | 50 | MG | CAPSULE, HARD | ||||||||
104509602 | 10450960 | 3 | SS | SUTENT | SUNITINIB MALATE | 1 | UNK | 21938 | CAPSULE, HARD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
104509602 | 10450960 | 1 | Gastrointestinal stromal tumour |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
104509602 | 10450960 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
104509602 | 10450960 | Cardiac flutter | |
104509602 | 10450960 | Dyspnoea |
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 |
---|---|---|---|---|---|---|
104509602 | 10450960 | 2 | 20140804 | 0 |