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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523388 | 7234928 | I | 6523388-4 | 20091222 | 20091231 | EXP | JP-ROCHE-676720 | ROCHE | 77 | YR | M | Y | 20091231 | MD | JAPAN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523388 | 1012885608 | PS | VESANOID | 1 | ORAL | 020438 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6523388 | 1012885608 | ACUTE PROMYELOCYTIC LEUKAEMIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6523388 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 6523388 | ASCITES |
| 6523388 | SEPSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |