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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5689098 | 6601998 | I | 5689098-0 | 19760101 | 20080331 | EXP | GR-ROCHE-760117077001 | ROCHE | 27 | YR | F | Y | 20080331 | MD | GREECE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5689098 | 1009727663 | PS | VALIUM | 1 | ORAL | 013263 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5689098 | 1009727663 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
5689098 | DE |
Reactions reported
Event ID | PT |
---|---|
5689098 | DEATH |
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 |
---|---|---|---|---|---|
5689098 | 1009727663 | 1 | DAY |