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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5375201 | 6298288 | F | 5375201-9 | 20070101 | 20070626 | 20070629 | EXP | US-ASTRAZENECA-2007UW08047 | AZPRODUW00 | 51 | YR | F | Y | 20070629 | 20070402 | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5375201 | 1008648572 | PS | FASLODEX | 1 | ORAL | 021344 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5375201 | 1008648572 | BREAST CANCER RECURRENT |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5375201 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 5375201 | DEATH |
| 5375201 | LIVER FUNCTION TEST ABNORMAL |
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 |
|---|---|---|---|---|---|
| 5375201 | 1008648572 | 20061201 | 20070201 | 2 | MON |