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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7299192 | 7368827 | F | 7299192-9 | 19980101 | 20110209 | 20110217 | EXP | US-PFIZER INC-2010050391 | PFIZERINC | 39 | YR | F | Y | 83.9 | KG | 20110216 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7299192 | 1015807204 | PS | ZOLOFT | 1 | 50 MG, DAILY | 019839 | |||||
| 7299192 | 1015807206 | C | AMBIEN | 1 | UNK | ||||||
| 7299192 | 1015807207 | C | XANAX | 1 | UNK | ||||||
| 7299192 | 1015807208 | C | SOMA | 1 | UNK | ||||||
| 7299192 | 1015807209 | C | CODEINE | 2 | |||||||
| 7299192 | 1015807205 | SS | PRISTIQ | 1 | 50 MG, 1X/DAY | 021992 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7299192 | 1015807204 | DEPRESSION |
| 7299192 | 1015807206 | INSOMNIA |
| 7299192 | 1015807205 | DEPRESSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7299192 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7299192 | DYSMENORRHOEA |
| 7299192 | HEADACHE |
| 7299192 | DRY MOUTH |
| 7299192 | CONSTIPATION |
| 7299192 | OROPHARYNGEAL BLISTERING |
| 7299192 | GALLBLADDER DISORDER |
| 7299192 | ABDOMINAL PAIN UPPER |
| 7299192 | ABDOMINAL PAIN |
| 7299192 | WEIGHT INCREASED |
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 |
|---|---|---|---|---|---|
| 7299192 | 1015807204 | 19980101 | |||
| 7299192 | 1015807205 | 20100414 |