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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6316798 | 7086790 | I | 6316798-1 | 20090501 | 20090817 | 20090820 | EXP | PHHY2009FR32783 | NOVARTIS PHARMACEUTICALS CORP. | 34 | YR | M | Y | 20090820 | LW | 20090501 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6316798 | 1012079499 | PS | LEPONEX | 2 | ORAL | UNK | 19758 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6316798 | 1012079499 | DEPRESSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6316798 | DE |
| 6316798 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6316798 | BALANCE DISORDER |
| 6316798 | FALL |
| 6316798 | GENERAL PHYSICAL HEALTH DETERIORATION |
| 6316798 | IMPAIRED SELF-CARE |
| 6316798 | MOVEMENT DISORDER |
| 6316798 | SUDDEN DEATH |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |