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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6031466 | 6887668 | I | 6031466-1 | 20081029 | 20081231 | PER | 179694USA | TEVA PHARMACEUTICALS USA | N | 20081216 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6031466 | 1010963870 | PS | SERTRALINE HYDROCHLORIDE | 1 | (25 MG) | 75719 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6031466 | OT |
Reactions reported
Event ID | PT |
---|---|
6031466 | DRUG EFFECT DECREASED |
6031466 | HALLUCINATION |
6031466 | HYPERTENSION |
6031466 | IRRITABILITY |
6031466 | SUICIDAL IDEATION |
6031466 | SUICIDE ATTEMPT |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6031466 | HP |
Therapies reported
no results found |