Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5119581 | 6144842 | I | 5119581-8 | 20060101 | 20060905 | 20060929 | EXP | 2006115117 | PFIZER INC | N | 20060928 | MD | GERMANY |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
5119581 | 1007725123 | PS | SUTENT | 1 | ORAL | 50 MG (50 MG,1 IN 1 D), ORAL | U | U | 21968 | ||
5119581 | 1007746635 | SS | FORTECORTIN (DEXAMETHASONE) | 2 | 10 MG (10 MG,1 IN 1 D) | U | U |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5119581 | 1007725123 | RENAL CELL CARCINOMA STAGE UNSPECIFIED |
5119581 | 1007746635 | RENAL CELL CARCINOMA STAGE UNSPECIFIED |
Outcome of event
Event ID | OUTC COD |
---|---|
5119581 | OT |
Reactions reported
Event ID | PT |
---|---|
5119581 | DRUG INEFFECTIVE |
5119581 | DRUG INTERACTION |
5119581 | METASTASES TO LUNG |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5119581 | FGN |
5119581 | HP |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5119581 | 1007725123 | 20060401 |