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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119947806 | 11994780 | 6 | F | 2015 | 20160912 | 20160203 | 20160913 | EXP | AR-PFIZER INC-2016001921 | PFIZER | 70.00 | YR | F | Y | 0.00000 | 20160913 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 119947806 | 11994780 | 1 | PS | SUTENT | SUNITINIB MALATE | 1 | 50 MG, CYCLIC (4/2) | Y | 420AB | 21938 | 50 | MG | CAPSULE, HARD | ||||||
| 119947806 | 11994780 | 2 | SS | SUTENT | SUNITINIB MALATE | 1 | UNK | Y | 991PC | 21938 | CAPSULE, HARD | ||||||||
| 119947806 | 11994780 | 3 | SS | SUTENT | SUNITINIB MALATE | 1 | UNK | Y | 68CPC | 21938 | CAPSULE, HARD | ||||||||
| 119947806 | 11994780 | 4 | SS | SUTENT | SUNITINIB MALATE | 1 | 37.5 MG, CYCLIC | Y | 680AD | 21938 | 37.5 | MG | CAPSULE, HARD | ||||||
| 119947806 | 11994780 | 5 | SS | SUTENT | SUNITINIB MALATE | 1 | UNK | Y | 21938 | CAPSULE, HARD | |||||||||
| 119947806 | 11994780 | 6 | SS | SUTENT | SUNITINIB MALATE | 1 | UNK | Y | 21938 | CAPSULE, HARD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 119947806 | 11994780 | 1 | Metastatic renal cell carcinoma |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 119947806 | 11994780 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 119947806 | 11994780 | Amnesia | |
| 119947806 | 11994780 | Anxiety | |
| 119947806 | 11994780 | Blood potassium decreased | |
| 119947806 | 11994780 | Blood pressure fluctuation | |
| 119947806 | 11994780 | Blood pressure increased | |
| 119947806 | 11994780 | Blood sodium decreased | |
| 119947806 | 11994780 | Burning sensation | |
| 119947806 | 11994780 | Condition aggravated | |
| 119947806 | 11994780 | Coordination abnormal | |
| 119947806 | 11994780 | Decreased immune responsiveness | |
| 119947806 | 11994780 | Diabetes mellitus | |
| 119947806 | 11994780 | Disease progression | |
| 119947806 | 11994780 | Erythema | |
| 119947806 | 11994780 | Loss of consciousness | |
| 119947806 | 11994780 | Lung infection | |
| 119947806 | 11994780 | Malaise | |
| 119947806 | 11994780 | Metastatic renal cell carcinoma | |
| 119947806 | 11994780 | Pain | |
| 119947806 | 11994780 | Pruritus | |
| 119947806 | 11994780 | Rash | |
| 119947806 | 11994780 | Skin exfoliation | |
| 119947806 | 11994780 | Skin lesion | |
| 119947806 | 11994780 | Skin sensitisation | |
| 119947806 | 11994780 | Stomatitis | |
| 119947806 | 11994780 | Syncope | |
| 119947806 | 11994780 | Time perception altered | |
| 119947806 | 11994780 | Urinary tract infection | |
| 119947806 | 11994780 | Visual impairment | |
| 119947806 | 11994780 | 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 |
|---|---|---|---|---|---|---|
| 119947806 | 11994780 | 1 | 20151204 | 20160105 | 0 | |
| 119947806 | 11994780 | 5 | 20160318 | 0 | ||
| 119947806 | 11994780 | 6 | 20160530 | 0 |