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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5041736 | 6080429 | I | 5041736-1 | 20060622 | 20060630 | EXP | 2006080203 | PFIZER INC | N | 20060629 | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5041736 | 1007435649 | PS | NEURONTIN | 1 | D | D | 20235 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5041736 | 1007435649 | BACK PAIN |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5041736 | DE |
| 5041736 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5041736 | COMPLETED SUICIDE |
| 5041736 | SUICIDAL IDEATION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5041736 | CSM |
Therapies reported
| no results found |