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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5375200 | 6346142 | F | 5375200-7 | 20060601 | 20070314 | 20070629 | PER | US-ASTRAZENECA-2007UW01990 | AZPRODUW00 | 72 | YR | F | Y | 81.6 | KG | 20070629 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5375200 | 1008648570 | PS | TAMOXIFEN CITRATE | 1 | ORAL | 017970 | |||||
| 5375200 | 1008648571 | C | GLUCOVANCE | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5375200 | 1008648570 | BREAST CANCER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5375200 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5375200 | THROMBOSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |