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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5195455 | 6206062 | I | 5195455-1 | 20061012 | 20061222 | 20061230 | EXP | FR-ABBOTT-06P-056-0354221-00 | ABBOTT | M | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5195455 | 1007999523 | PS | VALPROATE SODIUM | 1 | ORAL | UNKNOWN | 018723 | ||||
| 5195455 | 1007999524 | SS | VALPROATE SODIUM | 1 | ORAL | UNKNOWN | 018723 | ||||
| 5195455 | 1007999525 | C | ZOPICLONE | 2 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5195455 | 1007999523 | AFFECTIVE DISORDER |
| 5195455 | 1007999525 | SLEEP DISORDER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5195455 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5195455 | HEARING IMPAIRED |
| 5195455 | HYPOACUSIS |
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 |
|---|---|---|---|---|---|
| 5195455 | 1007999523 | 20021201 | 20061001 | ||
| 5195455 | 1007999524 | 20061001 | |||
| 5195455 | 1007999525 | 20020101 |