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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523651 | 7235081 | I | 6523651-7 | 20091106 | 20091228 | 20091231 | EXP | PHHY2009FR58988 | NOVARTIS PHARMACEUTICAL CORPORATION | 79 | F | Y | 20091231 | OT | FRANCE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523651 | 1012886612 | PS | FEMARA | 1 | ORAL | UNK | 020726 | ||||
| 6523651 | 1012886613 | C | NITRENDIPINE | 2 | |||||||
| 6523651 | 1012886614 | C | INFLUENZA VACCINE | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6523651 | 1012886612 | BREAST CANCER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6523651 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6523651 | C-REACTIVE PROTEIN INCREASED |
| 6523651 | CYTOLYTIC HEPATITIS |
| 6523651 | ERYTHEMA MULTIFORME |
| 6523651 | INFLAMMATION |
| 6523651 | ORAL DISORDER |
| 6523651 | PRURITUS |
| 6523651 | PYREXIA |
| 6523651 | RASH |
| 6523651 | SKIN LESION |
| 6523651 | THROMBOCYTOPENIA |
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 |
|---|---|---|---|---|---|
| 6523651 | 1012886612 | 20090815 | 20091109 | 87 | DAY |