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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5229968 | 6231317 | I | 5229968-0 | 20060731 | 20070206 | PER | US-GLAXOSMITHKLINE-A0614192A | GLAXOSMITHKLINE | M | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5229968 | 1008118460 | PS | PAXIL | 1 | ORAL | 20MG PER DAY | UNKNOWN | 020031 | |||
5229968 | 1008118461 | C | REMERON | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5229968 | 1008118460 | DEPRESSION |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
5229968 | ANXIETY |
5229968 | BLOOD PRESSURE INCREASED |
5229968 | POOR QUALITY SLEEP |
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 |
---|---|---|---|---|---|
5229968 | 1008118460 | 20010101 | 2 | YR |