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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126780131 | 12678013 | 1 | I | 20160817 | 20160823 | 20160823 | EXP | US-PFIZER INC-2016392940 | PFIZER | 0.00 | E | F | Y | 59.42000 | KG | 20160823 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126780131 | 12678013 | 1 | PS | DILANTIN | PHENYTOIN | 1 | Oral | 200 MG, EVERY NIGHT | 84349 | 200 | MG | CAPSULE, HARD | QD | ||||||
| 126780131 | 12678013 | 2 | C | METOPROLOL. | METOPROLOL | 1 | 50 MG, 1X/DAY | 0 | 50 | MG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126780131 | 12678013 | 1 | Seizure |
| 126780131 | 12678013 | 2 | Blood pressure abnormal |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126780131 | 12678013 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126780131 | 12678013 | Condition aggravated | |
| 126780131 | 12678013 | Dementia Alzheimer's type | |
| 126780131 | 12678013 | Drug ineffective | |
| 126780131 | 12678013 | Fall |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |