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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6809625 | 6909714 | F | 6809625-7 | 20060901 | 20100621 | 20100630 | EXP | US-PFIZER INC-2006118865 | PFIZERINC | 65 | YR | F | Y | 62.6 | KG | 20100630 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6809625 | 1014004277 | PS | CHANTIX | 1 | 0.5 MG, UNK | 021928 | |||||
| 6809625 | 1014004278 | C | BENADRYL | 1 | UNK | ||||||
| 6809625 | 1014004279 | C | REMERON | 1 | UNK | ||||||
| 6809625 | 1014004280 | C | REMERON | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6809625 | 1014004278 | HYPERSENSITIVITY |
| 6809625 | 1014004279 | INSOMNIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6809625 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6809625 | DEPRESSION |
| 6809625 | MEMORY IMPAIRMENT |
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 |
|---|---|---|---|---|---|
| 6809625 | 1014004277 | 20060901 |