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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7914581 | 8244856 | I | 7914581-4 | 20110915 | 20111104 | 20111115 | EXP | PHEH2011US008740 | NOVARTIS PHARMACEUTICAL CORPORATION | 57 | YR | M | Y | 20111115 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7914581 | 1018048302 | PS | MYFORTIC | 1 | ORAL | 360 MG, BID | 050791 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7914581 | 1018048302 | RENAL TRANSPLANT |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7914581 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 7914581 | LIMB DISCOMFORT |
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 |
|---|---|---|---|---|---|
| 7914581 | 1018048302 | 20110531 |