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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5230222 | 6231558 | I | 5230222-1 | 20050501 | 20061006 | 20070206 | PER | US-GLAXOSMITHKLINE-A0622776A | GLAXOSMITHKLINE | 33 | YR | F | Y | 20070206 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5230222 | 1008119123 | PS | PAXIL CR | 1 | ORAL | 25MG PER DAY | UNKNOWN | 020936 | |||
5230222 | 1008119124 | C | COPAXONE | 1 | |||||||
5230222 | 1008119125 | C | ORLISTAT | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5230222 | 1008119123 | DEPRESSION |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
5230222 | CRYING |
5230222 | DIZZINESS |
5230222 | NAUSEA |
5230222 | SENSORY DISTURBANCE |
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 |
---|---|---|---|---|---|
5230222 | 1008119123 | 20030101 |