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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4524411 | 5695232 | I | 4524411-9 | 20040914 | 20041117 | PER | SUS1-2004-00569 | SHIRE PHARMACEUTICAL DEVELOPMENT INC. | F | N | 20041115 | MD |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4524411 | 1005480450 | PS | CARBATROL | 1 | U | U | 20712 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
4524411 | OT |
Reactions reported
Event ID | PT |
---|---|
4524411 | STEVENS-JOHNSON SYNDROME |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4524411 | HP |
Therapies reported
no results found |