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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7583761 | 8017034 | I | 7583761-2 | 20110622 | 20110630 | EXP | CH-ROCHE-785304 | ROCHE | YR | M | Y | 20110630 | OT | SWITZERLAND |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7583761 | 1016905418 | PS | ISOTRETINOIN | 1 | ORAL | 018662 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
7583761 | DE |
Reactions reported
Event ID | PT |
---|---|
7583761 | COMPLETED SUICIDE |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |