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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4785951 | 5893921 | I | 4785951-0 | 20021205 | 20050916 | 20050930 | EXP | SUS1-2005-00700 | SHIRE DEVELOPMENT INC. | 20 | YR | F | N | 20050927 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4785951 | 1006476341 | PS | PENTASA | 1 | ORAL | ORAL | Y | D | 20049 | ||
| 4785951 | 1006495583 | C | PREDNISONE | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4785951 | 1006476341 | COLITIS ULCERATIVE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4785951 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4785951 | VASCULITIS CEREBRAL |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4785951 | FGN |
| 4785951 | HP |
| 4785951 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4785951 | 1006476341 | 20020101 |