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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6809881 | 7448694 | I | 6809881-5 | 20100531 | 20100618 | 20100630 | EXP | GB-WATSON-2010-08550 | WATSON | 37 | YR | F | Y | 50.6 | KG | 20100630 | OT | UNITED KINGDOM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6809881 | 1014005282 | PS | LAMOTRIGINE | 1 | ORAL | 25 MG, Q 2 DAYS | UNCONFIRMED | 076928 | |||
| 6809881 | 1014005283 | C | VALPROATE SODIUM | 1 | 900 MG, BID |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6809881 | 1014005282 | EPILEPSY |
| 6809881 | 1014005283 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6809881 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6809881 | DECREASED APPETITE |
| 6809881 | ERYTHEMA |
| 6809881 | LETHARGY |
| 6809881 | LIP BLISTER |
| 6809881 | LIP SWELLING |
| 6809881 | MOBILITY DECREASED |
| 6809881 | MOUTH ULCERATION |
| 6809881 | RASH PAPULAR |
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 |
|---|---|---|---|---|---|
| 6809881 | 1014005282 | 20100521 | 20100603 | 13 | DAY |