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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6918679 | 7476233 | F | 6918679-9 | 20100618 | 20100728 | 20100811 | EXP | PHHY2010US40235 | NOVARTIS PHARMACEUTICAL CORPORATION | 57 | YR | M | Y | 89.1 | KG | 20100811 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6918679 | 1014390750 | PS | EXJADE | 1 | ORAL | 1000 MG, QD | 021882 | ||||
| 6918679 | 1014390751 | C | BLOOD CELLS, PACKED HUMAN | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6918679 | 1014390750 | MYELODYSPLASTIC SYNDROME |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6918679 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6918679 | DIARRHOEA |
| 6918679 | FEBRILE NEUTROPENIA |
| 6918679 | KNEE OPERATION |
| 6918679 | NAUSEA |
| 6918679 | VISUAL IMPAIRMENT |
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 |
|---|---|---|---|---|---|
| 6918679 | 1014390750 | 20100611 | 20100618 | 8 | DAY |