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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8602292 | 8738407 | I | 8602292-1 | 20090421 | 20120423 | PER | PHEH2009US04008 | NOVARTIS PHARMACEUTICALS CORP. | 79 | YR | F | N | 20090730 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8602292 | 1020590547 | PS | FEMARA | 1 | 20726 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8602292 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8602292 | FATIGUE |
| 8602292 | BONE PAIN |
| 8602292 | ARTHRITIS |
| 8602292 | ARTHRALGIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 8602292 | CSM |
Therapies reported
| no results found |