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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523653 | 7048841 | F | 6523653-0 | 20081025 | 20091228 | 20091231 | EXP | PHHY2009FR27026 | NOVARTIS PHARMACEUTICAL CORPORATION | 48 | YR | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523653 | 1012886616 | PS | FEMARA | 1 | ORAL | 2.5 MG | 20726 | ||||
| 6523653 | 1012886617 | SS | FEMARA | 1 | ORAL | UNK | 020726 | ||||
| 6523653 | 1012886618 | SS | ESCITALOPRAM | 1 | ORAL | UNK | |||||
| 6523653 | 1012886619 | SS | TERCIAN | 2 | ORAL | UNK | |||||
| 6523653 | 1012886620 | SS | PRAZEPAM | 1 | ORAL | UNK | |||||
| 6523653 | 1012886621 | SS | SECTRAL | 1 | ORAL | UNK |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6523653 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6523653 | BALANCE DISORDER |
| 6523653 | CEREBELLAR SYNDROME |
| 6523653 | EYE PAIN |
| 6523653 | INTRACRANIAL PRESSURE INCREASED |
| 6523653 | MENINGEAL DISORDER |
| 6523653 | SCOTOMA |
| 6523653 | SPINAL CORD INJURY |
| 6523653 | VERTIGO |
| 6523653 | VISION BLURRED |
| 6523653 | VISUAL ACUITY REDUCED |
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 |
|---|---|---|---|---|---|
| 6523653 | 1012886616 | 20010615 | |||
| 6523653 | 1012886618 | 20070401 | |||
| 6523653 | 1012886619 | 20070901 | |||
| 6523653 | 1012886620 | 20030101 | |||
| 6523653 | 1012886621 | 20010101 |