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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5117313 | 6138942 | I | 5117313-0 | 20060801 | 20060925 | 20060929 | EXP | PHEH2006US12147 | NOVARTIS PHARMACEUTICALS CORP. | 97 | YR | F | Y | 51.247 | KG | 20060929 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5117313 | 1007715811 | PS | EXJADE | 1 | ORAL | 1000 MG, QD | 021882 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5117313 | DE |
5117313 | HO |
Reactions reported
Event ID | PT |
---|---|
5117313 | DEATH |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |