Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125486311 | 12548631 | 1 | I | 20151104 | 20160712 | 20160712 | PER | US-TEVA-607136USA | TEVA | 0.00 | F | Y | 0.00000 | 20160712 | CN | US | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125486311 | 12548631 | 1 | PS | LAMOTRIGINE. | LAMOTRIGINE | 1 | 300 MILLIGRAM DAILY; | 76420 | 150 | MG | TABLET | BID | |||||||
| 125486311 | 12548631 | 2 | SS | EPILIM | VALPROATE SODIUM | 1 | Unknown | 1800 MILLIGRAM DAILY; | 0 | 900 | MG | BID | |||||||
| 125486311 | 12548631 | 3 | SS | KEPPRA | LEVETIRACETAM | 1 | Unknown | 4000 MILLIGRAM DAILY; | 0 | 2000 | MG | BID |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125486311 | 12548631 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125486311 | 12548631 | Fatigue | |
| 125486311 | 12548631 | Seizure |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |