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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5282286 | 6276607 | I | 5282286-7 | 20070301 | 20070320 | 20070331 | EXP | FR-PFIZER INC-2007023422 | PFIZER INC | 69 | YR | Y | 20070330 | MD | FRANCE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5282286 | 1008316826 | PS | NEURONTIN | 1 | DAILY DOSE:3600MG | 020235 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5282286 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5282286 | CHOLESTASIS |
| 5282286 | CYTOLYTIC HEPATITIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |