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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5195461 | 6206066 | I | 5195461-7 | 20061021 | 20061219 | 20061230 | EXP | CN-ABBOTT-06P-035-0353642-00 | ABBOTT | F | Y | 20061230 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5195461 | 1007999570 | PS | DEPAKENE | 1 | ORAL | UNKNOWN | 018081 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5195461 | 1007999570 | EPILEPSY |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5195461 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5195461 | BLOOD FIBRINOGEN DECREASED |
| 5195461 | CEREBRAL HAEMORRHAGE |
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 |
|---|---|---|---|---|---|
| 5195461 | 1007999570 | 20061021 | 20061106 |