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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5117317 | 6123963 | F | 5117317-8 | 20060818 | 20060827 | 20060929 | EXP | DE-BAYER-200611127BVD | BAYER PHARMACEUTICALS CORPORATION | 64 | YR | M | Y | 20060929 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5117317 | 1007715817 | PS | NEXAVAR | 1 | ORAL | 21923 | |||||
| 5117317 | 1007715818 | C | IBUPROFEN | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5117317 | 1007715817 | UNEVALUABLE EVENT |
| 5117317 | 1007715818 | UNEVALUABLE EVENT |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5117317 | HO |
| 5117317 | LT |
Reactions reported
| Event ID | PT |
|---|---|
| 5117317 | RENAL FAILURE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5117317 | 1007715817 | 20060812 |