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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126639552 | 12663955 | 2 | F | 201607 | 20160819 | 20160818 | 20160819 | EXP | US-PFIZER INC-2016387315 | PFIZER | 37.00 | YR | M | Y | 78.93000 | KG | 20160819 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126639552 | 12663955 | 1 | PS | DILANTIN | PHENYTOIN | 1 | Oral | 500 MG DAILY (100MG CAPSULE, TWO IN THE MORNING AND THREE AT NIGHT) | 84349 | CAPSULE, HARD | BID | ||||||||
| 126639552 | 12663955 | 2 | SS | KEPPRA | LEVETIRACETAM | 1 | 750 MG, 2X/DAY (750MG ONE IN THE MORNING AND ONE AT NIGHT) | 0 | 750 | MG | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126639552 | 12663955 | 1 | Seizure |
| 126639552 | 12663955 | 2 | Seizure |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126639552 | 12663955 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126639552 | 12663955 | Condition aggravated | |
| 126639552 | 12663955 | Fall | |
| 126639552 | 12663955 | Seizure |
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 |
|---|---|---|---|---|---|---|
| 126639552 | 12663955 | 1 | 2005 | 0 | ||
| 126639552 | 12663955 | 2 | 201605 | 201607 | 0 |