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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5230995 | 5784689 | F | 5230995-8 | 20030901 | 20070131 | 20070206 | EXP | GB-GLAXOSMITHKLINE-B0361174A | GLAXOSMITHKLINE | F | Y | 20070206 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5230995 | 1008121299 | PS | PAROXETINE HYDROCHLORIDE | 1 | UNKNOWN | 20MG PER DAY | 020031 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5230995 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5230995 | CRYING |
| 5230995 | DRUG WITHDRAWAL SYNDROME |
| 5230995 | SUICIDAL IDEATION |
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 |
|---|---|---|---|---|---|
| 5230995 | 1008121299 | 19980127 | 20030901 | YR |