Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5282282 | 6276602 | I | 5282282-X | 20060601 | 20070319 | 20070331 | EXP | CA-PFIZER INC-2007023368 | PFIZER INC | 59 | YR | M | Y | 20070330 | CN | CANADA |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5282282 | 1008316813 | PS | DILANTIN | 1 | ORAL | DAILY DOSE:400MG | 084427 | ||||
| 5282282 | 1008316814 | C | LIPITOR | 1 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5282282 | 1008316813 | GRAND MAL CONVULSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5282282 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5282282 | ABDOMINAL PAIN |
| 5282282 | ARTHRALGIA |
| 5282282 | CONSTIPATION |
| 5282282 | CONVULSION |
| 5282282 | DYSARTHRIA |
| 5282282 | EYE ROLLING |
| 5282282 | FRACTURE |
| 5282282 | HAEMATOCHEZIA |
| 5282282 | VOMITING |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |