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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6250366 | 6968824 | F | 6250366-5 | 20080228 | 20090625 | 20090630 | EXP | PHHO2009NL03619 | NOVARTIS PHARMACEUTICALS CORP. | 40 | M | Y | 20090629 | MD | NETHERLANDS |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6250366 | 1011810925 | PS | CYCLOSPORINE | 1 | ORAL | UNK | 50715 | ||||
| 6250366 | 1011810926 | SS | CYCLOSPORINE | 1 | ORAL | UNK | 050715 | ||||
| 6250366 | 1011810927 | SS | NO TREATMENT RECEIVED NOMED | 2 | ORAL | UNK | |||||
| 6250366 | 1011810928 | SS | TACROLIMUS | 1 | ORAL | UNK | |||||
| 6250366 | 1011810929 | SS | TACROLIMUS | 1 | ORAL | UNK |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6250366 | 1011810925 | LIVER TRANSPLANT |
| 6250366 | 1011810927 | LIVER TRANSPLANT |
| 6250366 | 1011810928 | LIVER TRANSPLANT |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6250366 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6250366 | B-CELL LYMPHOMA |
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 |
|---|---|---|---|---|---|
| 6250366 | 1011810925 | 20070517 | 20070525 | 9 | DAY |
| 6250366 | 1011810926 | 20070714 | 20080222 | 224 | DAY |
| 6250366 | 1011810928 | 20070601 | 20070603 | 3 | DAY |
| 6250366 | 1011810929 | 20070612 | 20070713 | 32 | DAY |