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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
114319193 | 11431919 | 3 | F | 20160913 | 20150828 | 20160919 | PER | US-PFIZER INC-2015274043 | PFIZER | 45.00 | YR | M | Y | 88.89000 | KG | 20160919 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
114319193 | 11431919 | 1 | PS | SUTENT | SUNITINIB MALATE | 1 | Oral | 50 MG, CYCLIC (FOR DAY 1 TO DAY 14 EVERY 21 DAYS) | Y | 21938 | 50 | MG | CAPSULE, HARD | ||||||
114319193 | 11431919 | 2 | SS | SUTENT | SUNITINIB MALATE | 1 | Oral | 50 MG, CYCLIC (DAY 1-14 Q21 DAYS) | Y | 753CA | 21938 | 50 | MG | CAPSULE, HARD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
114319193 | 11431919 | 1 | Renal cell carcinoma |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
114319193 | 11431919 | Diarrhoea | |
114319193 | 11431919 | Emotional disorder | |
114319193 | 11431919 | Fatigue | |
114319193 | 11431919 | Feeling abnormal | |
114319193 | 11431919 | Gastric disorder | |
114319193 | 11431919 | Lethargy |
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 |
---|---|---|---|---|---|---|
114319193 | 11431919 | 1 | 20150817 | 0 | ||
114319193 | 11431919 | 2 | 20160617 | 0 |