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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 128021581 | 12802158 | 1 | I | 20160805 | 0 | 20160930 | 20160930 | DIR | US-FDA-351977 | FDA-CTU | 39.43 | YR | F | N | 63.00000 | KG | 20160930 | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 128021581 | 12802158 | 1 | PS | LEVETIRACETAM. | LEVETIRACETAM | 1 | Oral | ? QUANTITY:4 TABLET(S);? | Y | D | 311369025700 | 20170726 | 0 | 4 | DF | COATED TABLET | QD | ||
| 128021581 | 12802158 | 2 | C | ESCITALOPRAM | ESCITALOPRAM OXALATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 128021581 | 12802158 | 1 | Epilepsy |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 128021581 | 12802158 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 128021581 | 12802158 | Epilepsy | |
| 128021581 | 12802158 | Fall | |
| 128021581 | 12802158 | Head injury |
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 |
|---|---|---|---|---|---|---|
| 128021581 | 12802158 | 1 | 20160725 | 20160909 | 0 |