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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7298896 | 7817060 | I | 7298896-1 | 20110207 | 20110217 | EXP | PHHY2011US11406 | NOVARTIS PHARMACEUTICAL CORPORATION | YR | F | Y | 64.86 | KG | 20110217 | CN | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7298896 | 1015806157 | PS | EXJADE | 1 | ORAL | 500 MG, TID | 021882 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7298896 | 1015806157 | IRON METABOLISM DISORDER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7298896 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7298896 | COLITIS ISCHAEMIC |
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 |
|---|---|---|---|---|---|
| 7298896 | 1015806157 | 20080108 |