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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126412751 | 12641275 | 1 | I | 20160729 | 20160810 | 20160810 | PER | US-PFIZER INC-2016369227 | PFIZER | 57.00 | YR | F | Y | 87.35000 | KG | 20160810 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126412751 | 12641275 | 1 | PS | DILANTIN | PHENYTOIN | 1 | Oral | 200 MG, 1X/DAY | U | 84349 | 200 | MG | CAPSULE, HARD | QD | |||||
| 126412751 | 12641275 | 2 | C | MYSOLINE | PRIMIDONE | 1 | Oral | 250 MG, 2X/DAY | 0 | 250 | MG | TABLET | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126412751 | 12641275 | 1 | Partial seizures |
| 126412751 | 12641275 | 2 | Partial seizures |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126412751 | 12641275 | Aura | |
| 126412751 | 12641275 | Drug dose omission |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |