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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5578161 | 6517274 | F | 5578161-0 | 20070724 | 20071217 | 20071231 | EXP | GB-PFIZER INC-2007102843 | PFIZER INC | M | Y | 95.6 | KG | 20071231 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5578161 | 1009350773 | PS | CHANTIX | 1 | ORAL | 021928 | |||||
| 5578161 | 1009350774 | C | DULOXETINE | 2 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5578161 | 1009350773 | EX-SMOKER |
| 5578161 | 1009350774 | DEPRESSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5578161 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5578161 | THERAPEUTIC RESPONSE UNEXPECTED |
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 |
|---|---|---|---|---|---|
| 5578161 | 1009350774 | 20070511 | 20070724 |