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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6662240 | 7309829 | F | 6662240-0 | 20090312 | 20100318 | 20100331 | EXP | CA-PFIZER INC-2010025332 | PFIZERINC | 73 | YR | F | Y | 20100330 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6662240 | 1013423822 | PS | LYRICA | 1 | ORAL | 25 MG, 1X/DAY AT BEDTIME | 021446 | ||||
| 6662240 | 1013423823 | C | TRAMADOL | 2 | 200 MG, 1X/DAY |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6662240 | 1013423822 | PAIN |
| 6662240 | 1013423823 | PAIN |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6662240 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6662240 | HYPERSENSITIVITY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6662240 | 1013423822 | 20090310 | 20090301 | ||
| 6662240 | 1013423823 | 20090310 |