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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6810391 | 7449110 | F | 6810391-X | 20100616 | 20100630 | EXP | PHHY2010JP37891 | NOVARTIS PHARMACEUTICAL CORPORATION | 6 | YR | M | Y | 20100630 | JAPAN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6810391 | 1014007689 | PS | TEGRETOL | 1 | UNK,UNK | 016608 | |||||
| 6810391 | 1014007690 | SS | TEGRETOL | 1 | 016608 | ||||||
| 6810391 | 1014007691 | C | VALPROATE SODIUM | 1 | UNK |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6810391 | 1014007689 | PETIT MAL EPILEPSY |
| 6810391 | 1014007690 | PARTIAL SEIZURES |
| 6810391 | 1014007691 | PETIT MAL EPILEPSY |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6810391 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6810391 | DISTURBANCE IN ATTENTION |
| 6810391 | PSYCHOMOTOR HYPERACTIVITY |
| 6810391 | STATUS EPILEPTICUS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |