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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122565303 | 12256530 | 3 | F | 2016 | 20160627 | 20160412 | 20160707 | EXP | AR-PFIZER INC-2016196048 | PFIZER | 57.00 | YR | M | Y | 0.00000 | 20160707 | CN | AR | AR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122565303 | 12256530 | 1 | PS | SUTENT | SUNITINIB MALATE | 1 | 50 MG, CYCLIC (4/2 SCHEME) | Y | 845BB | 21938 | 50 | MG | CAPSULE, HARD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122565303 | 12256530 | 1 | Metastatic renal cell carcinoma |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122565303 | 12256530 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122565303 | 12256530 | Ageusia | |
| 122565303 | 12256530 | Bone disorder | |
| 122565303 | 12256530 | Diarrhoea | |
| 122565303 | 12256530 | Gastrointestinal disorder | |
| 122565303 | 12256530 | Malaise | |
| 122565303 | 12256530 | Nausea | |
| 122565303 | 12256530 | Rheumatoid arthritis | |
| 122565303 | 12256530 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 122565303 | 12256530 | 1 | 20151111 | 0 |