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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 114351052 | 11435105 | 2 | F | 20160826 | 20150831 | 20160901 | PER | US-PFIZER INC-2015255176 | PFIZER | 0.00 | M | Y | 0.00000 | 20160901 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 114351052 | 11435105 | 1 | PS | SUTENT | SUNITINIB MALATE | 1 | 50 MG, 1X/DAY | 21938 | 50 | MG | CAPSULE, HARD | QD | |||||||
| 114351052 | 11435105 | 2 | SS | SUTENT | SUNITINIB MALATE | 1 | 37.5 MG, 1X/DAY | 21938 | 37.5 | MG | CAPSULE, HARD | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 114351052 | 11435105 | 1 | Renal cell carcinoma |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 114351052 | 11435105 | Dysgeusia | |
| 114351052 | 11435105 | Fatigue | |
| 114351052 | 11435105 | Laceration | |
| 114351052 | 11435105 | Pain in extremity | |
| 114351052 | 11435105 | Skin haemorrhage | |
| 114351052 | 11435105 | Yellow skin |
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 |
|---|---|---|---|---|---|---|
| 114351052 | 11435105 | 1 | 20150720 | 0 |