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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5117314 | 6102089 | F | 5117314-2 | 20060710 | 20060731 | 20060929 | EXP | PHEH2006US09891 | NOVARTIS PHARMACEUTICALS CORP. | 28 | YR | M | Y | 74.829 | KG | 20060929 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5117314 | 1007715812 | PS | EXJADE | 1 | ORAL | 1500 MG, QD | 21882 | ||||
| 5117314 | 1007715813 | C | HYDREA | 1 | 1000 MG, QD | ||||||
| 5117314 | 1007715814 | C | FOLIC ACID | 1 | 1 MG, QD |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5117314 | 1007715813 | SICKLE CELL ANAEMIA |
| 5117314 | 1007715814 | SICKLE CELL ANAEMIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5117314 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5117314 | ALANINE AMINOTRANSFERASE INCREASED |
| 5117314 | ASPARTATE AMINOTRANSFERASE INCREASED |
| 5117314 | BLOOD ALKALINE PHOSPHATASE INCREASED |
| 5117314 | BLOOD BILIRUBIN INCREASED |
| 5117314 | BLOOD LACTATE DEHYDROGENASE INCREASED |
| 5117314 | CHOLELITHIASIS |
| 5117314 | CHOLESTASIS |
| 5117314 | CHROMATURIA |
| 5117314 | HEPATITIS CHOLESTATIC |
| 5117314 | JAUNDICE |
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 |
|---|---|---|---|---|---|
| 5117314 | 1007715812 | 20060320 | 20060715 | 118 | DAY |