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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6255539 | 7048361 | I | 6255539-3 | 20090501 | 20090622 | 20090630 | EXP | 2009AL004193 | ACTAVIS ELIZABETH LLC | 41 | YR | M | N | 20090629 | OT | UNITED KINGDOM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6255539 | 1011834560 | PS | GABAPENTIN | 1 | ORAL | 900 MG; PO | D | D | 75694 | ||
| 6255539 | 1011875752 | C | ZONEGRAN | 1 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6255539 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6255539 | DRUG INTERACTION |
| 6255539 | MUTISM |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6255539 | CR |
| 6255539 | FGN |
| 6255539 | HP |
| 6255539 | OTH |
Therapies reported
| no results found |