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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123197973 | 12319797 | 3 | F | 20160629 | 20160429 | 20160705 | EXP | US-JNJFOC-20160319432 | JANSSEN | 0.00 | A | F | Y | 102.51000 | KG | 20160705 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123197973 | 12319797 | 1 | PS | TOPAMAX | TOPIRAMATE | 1 | Oral | U | U | UNKNOWN | 20505 | UNSPECIFIED | |||||||
| 123197973 | 12319797 | 2 | SS | KEPPRA | LEVETIRACETAM | 1 | Oral | Y | UNKNOWN | 0 | 750 | MG | UNSPECIFIED | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123197973 | 12319797 | 1 | Seizure |
| 123197973 | 12319797 | 2 | Seizure |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123197973 | 12319797 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123197973 | 12319797 | Anger | |
| 123197973 | 12319797 | Multiple sclerosis | |
| 123197973 | 12319797 | Seizure | |
| 123197973 | 12319797 | Suicidal ideation |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 123197973 | 12319797 | 2 | 20150818 | 20150915 | 0 |